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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 20 | 7 | 1 | 12 | 0 | 0 | 6 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001 | 1/1 | 387 | 336 | 79 | 48 | 157 | 12 | 38 | 125 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0002 | 0/0 | 387 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0003 | 0/0 | 387 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0004 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0005 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0006 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0007 | 0/0 | 387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1164 | 321 | 75 | 47 | 147 | 12 | 38 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0002 | 0/0 | 1164 | 13 | 7 | 1 | 5 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0003 | 0/0 | 1164 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0004 | 0/0 | 1164 | 7 | 0 | 0 | 7 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0005 | 0/0 | 1164 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0006 | 0/0 | 1164 | 4 | 2 | 1 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0007 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0008 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0009 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0010 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0011 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0012 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
c0013 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 271 | 214 | 65 | 34 | 86 | 8 | 20 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
t0002 | 1/0 | 271 | 152 | 27 | 18 | 84 | 4 | 18 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0002 | 0/0 | 1164 | 13 | 7 | 1 | 5 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0000c0004 | 0/0 | 1164 | 7 | 0 | 0 | 7 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0001 | 1/1 | 1164 | 321 | 75 | 47 | 147 | 12 | 38 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0003 | 0/0 | 1164 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0006 | 0/0 | 1164 | 4 | 2 | 1 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0010 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0013 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0002c0005 | 0/0 | 1164 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0003c0007 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0004c0008 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0005c0011 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0006c0012 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0007c0009 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0002t0001 | 0/0 | 1434 | 6 | 5 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0000c0002t0002 | 0/0 | 1434 | 7 | 2 | 0 | 5 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0000c0004t0001 | 0/0 | 1434 | 7 | 0 | 0 | 7 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0001t0001 | 0/1 | 1434 | 187 | 50 | 30 | 78 | 8 | 20 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0001t0002 | 1/0 | 1434 | 134 | 25 | 17 | 69 | 4 | 18 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0003t0002 | 0/0 | 1434 | 9 | 0 | 0 | 9 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0006t0001 | 0/0 | 1434 | 4 | 2 | 1 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0010t0001 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0001c0013t0001 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0002c0005t0001 | 0/0 | 1434 | 4 | 4 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0003c0007t0001 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0004c0008t0001 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0005c0011t0001 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0006c0012t0002 | 0/0 | 1434 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
a0007c0009t0002 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | copy fasta | chr16 | 82030253 | 82103534 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0004t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0000c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0150 | 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 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0311 | 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 |
a0001c0001t0001g0318 | 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 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0324 | 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 |
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 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0135 | 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 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0151 | 1/0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0003t0002g0130 | 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 |
a0001c0003t0002g0132 | 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 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0006t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0006t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0010t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0001c0013t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0002c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0002c0005t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0002c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0002c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0003c0007t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0003c0007t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0004c0008t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0005c0011t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0006c0012t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
a0007c0009t0002g0183 | 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 | g0267 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | FIN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00408 | hp1 | a0000 | c0004 | t0001 | g0010 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00438 | hp2 | a0000 | c0004 | t0001 | g0196 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00544 | hp1 | a0000 | c0004 | t0001 | g0010 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01109 | hp2 | a0000 | c0002 | t0001 | g0308 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01175 | hp2 | a0005 | c0011 | t0001 | g0228 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01192 | hp2 | a0006 | c0012 | t0002 | g0103 | 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 | g0076 | AMR | PUR | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01346 | hp1 | a0004 | c0008 | t0001 | g0286 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01433 | hp1 | a0001 | c0006 | t0001 | g0074 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0075 | 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 | g0043 | AMR | CLM | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0221 | 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 | a0000 | c0004 | t0001 | g0198 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02055 | hp1 | a0002 | c0005 | t0001 | g0322 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02071 | hp1 | a0000 | c0004 | t0001 | g0199 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02074 | hp1 | a0000 | c0004 | t0001 | g0152 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02129 | hp2 | a0001 | c0006 | t0001 | g0294 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02145 | hp1 | a0001 | c0006 | t0001 | g0058 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0268 | 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 | g0207 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02451 | hp1 | a0000 | c0002 | t0001 | g0314 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02630 | hp1 | a0001 | c0013 | t0001 | g0334 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02809 | hp2 | a0000 | c0002 | t0001 | g0317 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02818 | hp1 | a0002 | c0005 | t0001 | g0325 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02970 | hp1 | a0002 | c0005 | t0001 | g0315 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0330 | 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 | g0084 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03041 | hp1 | a0003 | c0007 | t0001 | g0335 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03130 | hp2 | a0003 | c0007 | t0001 | g0336 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03195 | hp1 | a0000 | c0002 | t0002 | g0042 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03209 | hp1 | a0002 | c0005 | t0001 | g0020 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03209 | hp2 | a0000 | c0002 | t0001 | g0306 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ESN | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0333 | 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 | a0000 | c0002 | t0001 | g0316 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03579 | hp2 | a0001 | c0010 | t0001 | g0161 | AFR | MSL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | STU | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0217 | 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 | g0001 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18943 | hp1 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18943 | hp2 | a0000 | c0004 | t0001 | g0197 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18944 | hp2 | a0000 | c0002 | t0002 | g0127 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18951 | hp1 | a0001 | c0003 | t0002 | g0109 | 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 | g0205 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0215 | 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 | g0017 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0120 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0067 | 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 | g0245 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18978 | hp1 | a0000 | c0002 | t0002 | g0169 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18978 | hp2 | a0001 | c0003 | t0002 | g0137 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18990 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18995 | hp1 | a0007 | c0009 | t0002 | g0183 | 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 | g0035 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19000 | hp1 | a0001 | c0003 | t0002 | g0130 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19006 | hp1 | a0000 | c0002 | t0002 | g0168 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19043 | hp2 | a0000 | c0002 | t0001 | g0329 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19068 | hp2 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0255 | 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 | g0214 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19088 | hp1 | a0000 | c0002 | t0002 | g0171 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19091 | hp2 | a0000 | c0002 | t0002 | g0123 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA19240 | hp2 | a0001 | c0006 | t0001 | g0082 | AFR | YRI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ASW | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ASW | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | GIH | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | GIH | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0126 | 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 | g0022 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
HG02559 | hp2 | a0000 | c0002 | t0002 | g0041 | AFR | ACB | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | LWK | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0211 | REF | REF | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0151 | REF | REF | HSD17B2_chr16_82030253_82103534 | HSD17B2 | chr16 | 82030253 | 82103534 |
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 | a0004 | 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 | a0006 | 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 | a0005 | 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 | a0000 | 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 |
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 | a0001c0013 | 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 | 2 | a0000c0004a0001c0006 | 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 | a0001c0010 | 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 |
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 | a0000c0002t0001a0000c0004t0001a0001c0001t0001others(7): Show | 214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
5_prime_UTR_variant | MODIFIER | c.-133T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/5 | 133 | chr16 | 82035292 |
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 | a0001c0001t0001g0021 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0019a0001c0001t0002g0312 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0022 | 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 | a0000c0002t0002g0041a0000c0002t0002g0042a0001c0001t0001g0056others(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 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0002g0031others(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 | a0001c0001t0001g0030a0001c0001t0002g0024a0001c0001t0002g0025others(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 | 26 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(23): 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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0184others(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 | a0000c0002t0001g0308a0000c0004t0001g0010a0000c0004t0001g0196others(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 | 14 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(11): Show | 14 | HG00735.hp1 HG00738.hp1 HG01169.hp1 others(11): 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 | 107 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(104): 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 | a0000c0002t0001g0306a0001c0001t0001g0305a0001c0001t0001g0345 | 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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0341 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0185 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0304 | 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 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 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 | a0000c0002t0001g0306 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0319 | 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 | a0001c0001t0002g0038 | 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 | a0001c0001t0001g0030a0001c0001t0001g0039 | 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 | 5 | a0001c0001t0001g0011a0001c0001t0001g0212a0001c0001t0001g0213others(2): 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 | a0001c0001t0001g0022a0001c0001t0002g0062 | 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0002g0037a0001c0001t0002g0059a0001c0001t0002g0153others(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 | a0000c0004t0001g0152 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | ||||||
chr16:82038001
|
T | C | 345 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(342): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.265+2312T>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82038001 | ||||||
chr16:82038119
|
G | T | 1 | a0001c0001t0001g0313 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0002g0186 | 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 | a0000c0004t0001g0010a0000c0004t0001g0196a0000c0004t0001g0197others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0002c0005t0001g0322 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0305others(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 | a0001c0001t0002g0024a0001c0001t0002g0031 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0338a0001c0001t0001g0344 | 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 | a0000c0002t0002g0041a0000c0002t0002g0042 | 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 | 130 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0004t0001g0010others(127): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): 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 | a0000c0004t0001g0199a0001c0001t0001g0345 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0001c0001t0002g0063 | 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 | 156 | a0000c0002t0001g0306a0000c0002t0001g0314a0000c0002t0001g0316others(153): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): 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 | a0000c0004t0001g0010a0000c0004t0001g0197a0000c0004t0001g0198others(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 | a0000c0004t0001g0196a0001c0001t0001g0013a0001c0001t0001g0174others(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 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0060others(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 | 113 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(110): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0002g0062 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0300a0001c0001t0001g0301 | 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0002g0149 | 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 | 309 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(306): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0002c0005t0001g0325 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0226a0001c0001t0001g0227a0005c0011t0001g0228 | 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 | a0001c0001t0002g0149 | 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 | a0001c0001t0002g0054 | 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 | a0001c0001t0001g0345 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0006t0001g0058 | 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 | a0000c0002t0001g0329a0001c0001t0001g0006a0001c0001t0001g0020others(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 | a0001c0001t0001g0302 | 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 | a0007c0009t0002g0183 | 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 | a0000c0004t0001g0152 | 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 | a0001c0001t0002g0068 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0000c0002t0001g0314 | 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 | a0001c0001t0002g0128 | 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 | a0001c0001t0001g0313 | 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 | a0000c0004t0001g0197 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | a0001c0001t0001g0030a0001c0001t0001g0039 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0039 | 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 | 118 | a0000c0002t0001g0306a0001c0001t0001g0001a0001c0001t0001g0009others(115): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): 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 | a0000c0002t0001g0329a0001c0001t0001g0006a0001c0001t0001g0020others(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 | a0000c0004t0001g0010a0000c0004t0001g0196a0000c0004t0001g0197others(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 | ||||||
chr16:82041851
|
C | T | 1 | a0001c0001t0001g0211 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.265+6162C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 1/4 | chr16 | 82041851 | ||||||
chr16:82041886
|
C | A | 48 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(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 | a0000c0004t0001g0010a0000c0004t0001g0196a0000c0004t0001g0197others(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 | a0000c0004t0001g0010a0000c0004t0001g0196a0000c0004t0001g0197others(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 | a0001c0001t0001g0313 | 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 | a0001c0001t0002g0025 | 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 | a0000c0004t0001g0010a0000c0004t0001g0197a0000c0004t0001g0198others(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 | 115 | a0000c0002t0001g0306a0001c0001t0001g0001a0001c0001t0001g0009others(112): Show | 125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): 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 | a0003c0007t0001g0335a0003c0007t0001g0336 | 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 | a0001c0001t0001g0340 | 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 | a0001c0006t0001g0058 | 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 | a0000c0002t0001g0329a0001c0001t0001g0006a0001c0001t0001g0020others(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 | a0001c0001t0002g0057 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0340 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0032 | 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0001g0230a0001c0001t0001g0231 | 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 | a0001c0001t0002g0031 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0043a0001c0001t0002g0071a0001c0001t0002g0072 | 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 | a0001c0006t0001g0294 | 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 | a0000c0002t0002g0042a0001c0001t0001g0001a0001c0001t0001g0009others(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 | a0000c0002t0001g0308a0000c0002t0002g0041a0000c0004t0001g0010others(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 | a0000c0004t0001g0152a0000c0004t0001g0196a0000c0004t0001g0198others(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 | a0000c0002t0001g0306 | 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 | a0001c0001t0001g0305 | 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 | 14 | a0000c0002t0002g0127a0000c0002t0002g0171a0001c0001t0001g0022others(11): Show | 14 | HG00741.hp1 HG02486.hp2 HG02965.hp1 others(11): 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 | a0000c0002t0001g0329a0001c0001t0001g0006a0001c0001t0001g0020others(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 | a0001c0001t0001g0345 | 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 | a0001c0006t0001g0294 | 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 | a0001c0001t0001g0298 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0319 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0002g0128 | 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 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0060others(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 | a0001c0006t0001g0294 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0079 | 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 | a0002c0005t0001g0322 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0150a0001c0001t0001g0217a0001c0001t0002g0055others(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 | a0000c0002t0001g0308a0000c0002t0001g0329a0000c0004t0001g0010others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0340 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0205 | 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 | 178 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(175): Show | 192 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(189): 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0319others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0319others(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 | a0000c0002t0002g0123a0001c0001t0002g0052a0001c0001t0002g0096others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0339a0001c0001t0002g0164 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0319 | 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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0319others(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 | 45 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(42): 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 | a0001c0001t0002g0043 | 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 | a0001c0006t0001g0058 | 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 | a0001c0001t0001g0340 | 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 | a0004c0008t0001g0286 | 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 | a0001c0001t0001g0022a0001c0001t0001g0323a0001c0001t0001g0324others(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 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0060others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0030a0001c0001t0001g0039 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0330a0001c0001t0001g0338a0001c0001t0001g0344others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0345 | 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 | a0002c0005t0001g0315 | 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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0341 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0175 | 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 | 187 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(184): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(197): 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 | a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0263 | 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 | 113 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(110): Show | 123 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(120): 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0319others(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 | 178 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(175): Show | 191 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(188): 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0302 | 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 | a0001c0006t0001g0058 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0002g0121 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0002g0046 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0122others(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 | a0001c0001t0001g0285 | 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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0005c0011t0001g0228 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0329a0001c0001t0001g0007a0001c0001t0001g0020others(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 | a0001c0001t0001g0311 | 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 | 3 | a0001c0003t0002g0109a0001c0003t0002g0110a0001c0003t0002g0120 | 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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0319others(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 | a0001c0001t0002g0149 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0060 | 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 | a0001c0003t0002g0130 | 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 | a0001c0001t0001g0264a0001c0001t0001g0265 | 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 | a0001c0001t0001g0342 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0185 | 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 | 8 | a0001c0003t0002g0109a0001c0003t0002g0110a0001c0003t0002g0120others(5): 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0001c0001t0001g0305 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0185 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0337 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | 113 | a0000c0002t0002g0041a0000c0002t0002g0042a0001c0001t0001g0001others(110): Show | 122 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(119): 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 | a0001c0003t0002g0130 | 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 | 300 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(297): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0340 | 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 | a0001c0001t0002g0099 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(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 | a0001c0001t0002g0062 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0002g0027 | 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 | a0001c0001t0002g0051 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0002g0026 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0002g0099 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0340 | 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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0001c0001t0002g0094a0001c0001t0002g0095 | 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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0022a0001c0001t0001g0313a0001c0001t0001g0323others(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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0021 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0000c0002t0002g0123 | 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 | a0001c0001t0001g0296a0001c0001t0001g0297 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177 | 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0034 | 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 | a0001c0003t0002g0130 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0305 | 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 | a0001c0001t0001g0240 | 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 | a0002c0005t0001g0325 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0210 | 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 | a0003c0007t0001g0335a0003c0007t0001g0336 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0002t0002g0041a0000c0002t0002g0042 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0313 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200others(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 | a0000c0002t0001g0306 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0001g0313 | 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 | a0000c0002t0001g0306a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0176a0001c0001t0001g0177 | 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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0020others(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 | a0000c0002t0001g0306a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0001c0001t0001g0338 | 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 | a0001c0001t0001g0338 | 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 | a0001c0001t0001g0309a0001c0001t0001g0311 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0002g0073 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0060 | 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0313 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0002g0051 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0185a0001c0001t0001g0194a0001c0001t0001g0278others(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 | a0000c0002t0001g0306a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0006t0001g0058a0001c0006t0001g0074a0001c0006t0001g0082 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0001t0001g0313 | 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 | a0001c0006t0001g0058a0001c0006t0001g0074a0001c0006t0001g0082 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(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 | a0000c0002t0001g0306 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0002g0079 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0277 | 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 | a0000c0004t0001g0152 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0002t0001g0306a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0001c0001t0002g0093 | 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 | 113 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(110): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0341 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0001c0001t0002g0182 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0204 | 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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0170a0001c0001t0001g0213a0001c0001t0001g0247others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0313 | 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 | 2 | a0001c0001t0002g0165a0001c0001t0002g0166 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0002g0138 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0022a0001c0001t0002g0186 | 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 | a0001c0001t0001g0022 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0003c0007t0001g0335 | 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 | a0001c0001t0002g0148 | 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 | 273 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(270): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0002g0063a0001c0001t0002g0139a0001c0001t0002g0140others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0001c0001t0001g0185 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0002g0028 | 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 | a0001c0001t0002g0107 | 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 | a0001c0001t0002g0148 | 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 | a0001c0006t0001g0058 | 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 | a0001c0001t0001g0039a0001c0001t0002g0139a0001c0001t0002g0140 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0261 | 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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0326others(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 | a0001c0001t0001g0239 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(113): Show | 125 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(122): 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0129 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | 266 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0002g0041others(263): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 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 | a0001c0001t0002g0065 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0002g0172 | 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 | a0000c0004t0001g0152 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | 11 | a0001c0001t0002g0037a0001c0001t0002g0059a0001c0001t0002g0135others(8): 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 | a0000c0002t0001g0308a0001c0001t0001g0022 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0187a0001c0001t0001g0188 | 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 | a0001c0001t0002g0051 | 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0308 | 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 | a0000c0002t0002g0127a0000c0002t0002g0168 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0313 | 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 | a0000c0002t0002g0171 | 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 | a0001c0001t0001g0305a0001c0001t0001g0309a0001c0001t0001g0310others(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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0342 | 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 | a0001c0001t0001g0323 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0345 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0002g0146 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0040others(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 | a0001c0001t0002g0065 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0006t0001g0058 | 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 | a0000c0002t0001g0308a0001c0001t0001g0006a0001c0001t0001g0160others(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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0002g0046 | 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 | a0001c0001t0001g0345 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0002g0084 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | 112 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(109): Show | 121 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(118): 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 | a0000c0002t0001g0308 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0329others(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 | 3 | a0001c0001t0002g0135a0001c0001t0002g0147a0007c0009t0002g0183 | 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 | a0001c0013t0001g0334 | 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 | a0001c0001t0001g0345 | 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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0006others(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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0020others(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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(107): Show | 119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): 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 | a0001c0001t0002g0046 | 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 | a0001c0001t0002g0046 | 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 | a0000c0004t0001g0152 | 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 | a0005c0011t0001g0228 | 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 | a0000c0002t0001g0306a0001c0001t0002g0126 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0249 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0013t0001g0334 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0000c0002t0001g0316a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0185 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0192 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0006t0001g0058 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0000c0002t0001g0308a0001c0001t0001g0006a0001c0001t0001g0160others(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 | a0000c0004t0001g0152 | 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 | 108 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(105): Show | 117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): 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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0006others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0000c0002t0001g0306 | 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 | a0000c0002t0001g0317 | 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 | a0001c0001t0002g0054 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0340a0001c0001t0002g0108 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0002g0051a0001c0001t0002g0071 | 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 | a0000c0002t0001g0308a0000c0002t0001g0314a0000c0002t0001g0316others(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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(107): Show | 119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0309a0001c0001t0001g0311 | 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 | a0001c0001t0001g0229 | 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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0326others(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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0278a0001c0001t0001g0291 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0006t0001g0058a0001c0006t0001g0074a0001c0006t0001g0082 | 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 | 182 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(179): Show | 194 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(191): 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0006t0001g0058a0001c0006t0001g0074a0001c0006t0001g0082 | 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 | a0001c0001t0001g0339a0001c0013t0001g0334 | 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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0006others(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 | a0001c0001t0001g0304 | 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 | a0001c0001t0002g0032 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0000c0002t0001g0308 | 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 | 112 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(109): Show | 121 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(118): 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0187a0001c0001t0001g0188 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0006others(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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0340others(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 | a0000c0002t0001g0308 | 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 | a0001c0001t0001g0223 | 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 | a0000c0004t0001g0197 | 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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0197others(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 | a0001c0001t0001g0056a0001c0001t0001g0278a0001c0001t0001g0291 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0302 | 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 | 2 | a0001c0001t0002g0135a0001c0001t0002g0147 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0030a0001c0001t0001g0039 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0002g0024a0001c0001t0002g0031 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0343 | 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 | a0001c0006t0001g0058a0001c0006t0001g0074a0001c0006t0001g0082 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0002g0085 | 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 | a0001c0001t0001g0022a0001c0001t0001g0185 | 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 | a0001c0001t0001g0345 | 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 | 2 | a0001c0001t0002g0135a0001c0001t0002g0147 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0001t0002g0071 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | 187 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(184): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.664+4742C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82075869 | ||||||
chr16:82075908
|
T | TA | 273 | a0000c0002t0001g0308a0000c0002t0001g0329a0000c0002t0002g0041others(270): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | 14 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0160others(11): 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0239a0001c0001t0001g0260a0001c0001t0001g0266 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0284 | 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0002g0071 | 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 | a0001c0001t0002g0045 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0203 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0002g0025 | 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 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0039others(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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0305 | 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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0004c0008t0001g0286 | 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 | 119 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(116): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0002t0001g0306 | 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 | 93 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(90): 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 | a0000c0002t0001g0308a0000c0002t0001g0329a0001c0001t0001g0006others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0229 | 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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0000c0002t0001g0306a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0006t0001g0058a0001c0006t0001g0074a0001c0006t0001g0082 | 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 | a0001c0001t0001g0259 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0313 | 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 | a0000c0002t0001g0308a0001c0001t0001g0006a0001c0001t0001g0160others(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 | a0001c0001t0001g0318 | 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 | a0000c0002t0001g0308a0001c0001t0001g0006a0001c0001t0001g0160others(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 | a0000c0002t0001g0308a0001c0001t0001g0006a0001c0001t0001g0160others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0000c0002t0001g0308 | 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 | a0001c0001t0002g0078 | 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 | a0000c0002t0001g0329a0001c0001t0001g0020a0001c0001t0001g0326others(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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0343a0001c0001t0002g0149 | 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 | a0001c0001t0002g0138 | 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 | a0001c0001t0001g0227 | 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 | a0000c0002t0001g0306a0001c0001t0001g0006a0001c0001t0001g0007others(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 | a0000c0002t0001g0314a0000c0002t0001g0316a0000c0002t0001g0317others(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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0001g0320a0001c0001t0002g0062 | 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 | a0000c0002t0001g0314 | 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 | 179 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(176): Show | 191 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(188): 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 | a0001c0001t0001g0192 | 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 | 6 | a0001c0001t0002g0004a0001c0001t0002g0089a0001c0001t0002g0104others(3): 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 | a0001c0001t0002g0026 | 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 | a0000c0002t0001g0308a0001c0001t0001g0007a0001c0001t0001g0030others(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 | a0001c0001t0001g0313 | 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 | a0001c0001t0001g0304 | 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 | a0000c0004t0001g0010a0000c0004t0001g0152a0000c0004t0001g0196others(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 | a0001c0001t0001g0185 | 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 | a0001c0001t0002g0069 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0020a0001c0001t0001g0326a0001c0001t0001g0327others(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 | 73 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(70): 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 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0242others(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 | a0000c0002t0001g0308a0000c0002t0002g0041a0000c0002t0002g0042 | 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 | a0001c0001t0002g0069 | 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 | 66 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(63): 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 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(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 | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(67): 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 | a0001c0001t0002g0038a0001c0001t0002g0178 | 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 | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(67): 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 | a0001c0006t0001g0082 | 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 | a0001c0001t0001g0185a0001c0013t0001g0334 | 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 | a0001c0001t0001g0341a0001c0001t0002g0055 | 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 | 109 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(106): 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 | a0001c0001t0001g0007a0001c0001t0001g0173a0001c0001t0001g0175others(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 | a0001c0006t0001g0082 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0077 | 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 | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(66): 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 | 60 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(57): Show | 62 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(59): 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 | a0001c0001t0001g0176a0001c0001t0001g0177 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0002g0062 | 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 | a0001c0001t0002g0052 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(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 | a0001c0001t0001g0257 | 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 | a0001c0001t0002g0084 | 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 | a0001c0001t0001g0175a0001c0001t0001g0200 | 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 | a0001c0001t0002g0055 | 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 | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(68): 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 | a0001c0001t0001g0030a0001c0001t0001g0039 | 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 | 63 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(60): Show | 65 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(62): 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 | a0001c0001t0002g0003 | 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0002g0045 | 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0002g0045 | 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 | a0001c0001t0001g0313a0001c0001t0001g0342 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0313others(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 | a0001c0001t0001g0302 | 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 | a0001c0001t0002g0003a0001c0001t0002g0083a0001c0001t0002g0090 | 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 | 48 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0020others(45): Show | 50 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(47): 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 | a0001c0001t0001g0256 | 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 | 5 | a0001c0001t0001g0203a0001c0001t0001g0235a0001c0001t0001g0253others(2): Show | 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 | 150 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(147): 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 | a0001c0001t0002g0052 | 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 | a0001c0006t0001g0082 | 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 | a0001c0001t0001g0006a0001c0001t0001g0160a0001c0001t0001g0162others(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 | 50 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0020others(47): Show | 52 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(49): 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 | a0001c0001t0001g0304 | 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 | a0000c0004t0001g0199 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 25 | a0001c0001t0001g0217a0001c0001t0001g0222a0001c0001t0001g0230others(22): 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 | a0001c0001t0002g0038a0001c0001t0002g0178 | 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 | 150 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(147): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0018a0001c0001t0001g0282 | 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 | 78 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.665-6132G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82084770 | ||||||
chr16:82084836
|
G | C | 67 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(64): Show | 69 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(66): 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0201 | 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 | 159 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(156): 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 | a0001c0001t0001g0245 | 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 | a0001c0006t0001g0082 | 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 | 43 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(40): Show | 45 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.665-5735C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085167 | ||||||
chr16:82085495
|
G | A | 47 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(44): Show | 49 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(46): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 71 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(68): Show | 74 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(71): 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 | a0001c0006t0001g0074 | 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 | a0001c0001t0002g0157 | 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 | 53 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(50): Show | 55 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(52): 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 | a0001c0001t0001g0313a0001c0001t0001g0342a0001c0006t0001g0082 | 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 | 52 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(49): Show | 54 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.665-5114T>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82085788 | ||||||
chr16:82085791
|
T | C | 56 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(53): Show | 58 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(55): 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 | a0001c0001t0001g0307 | 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 | 57 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(54): Show | 59 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(56): 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 | a0001c0001t0002g0045 | 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 | 158 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(155): 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 | a0001c0001t0002g0145 | 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 | 162 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(159): 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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0002g0045 | 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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0279a0001c0001t0001g0296a0001c0001t0001g0297 | 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 | a0001c0006t0001g0294 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0305a0001c0001t0001g0338a0001c0001t0001g0344 | 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 | 291 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(288): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.665-3104C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82087798 | ||||||
chr16:82087973
|
T | G | 304 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(301): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0001c0001t0002g0052 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 164 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(161): 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 | a0001c0001t0001g0289 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0002g0035 | 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 | 304 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(301): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0001c0001t0001g0331 | 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 | 344 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(341): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): 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 | a0001c0001t0002g0149 | 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 | 68 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(65): 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 | a0001c0006t0001g0082 | 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 | 9 | a0001c0003t0002g0053a0001c0003t0002g0109a0001c0003t0002g0110others(6): 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 | 165 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(162): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0002g0038 | 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 | 3 | a0001c0001t0002g0086a0001c0001t0002g0101a0001c0001t0002g0102 | 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 | a0001c0001t0001g0201a0001c0001t0001g0206 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0002g0045 | 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 | a0001c0001t0001g0285a0001c0001t0002g0049a0001c0001t0002g0088others(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 | a0001c0001t0002g0186 | 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 | 296 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(293): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.665-1212C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82089690 | ||||||
chr16:82090035
|
A | T | 297 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(294): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0001c0001t0001g0244a0001c0001t0001g0246 | 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 | a0001c0001t0001g0233 | 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 | 285 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(282): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.665-710C>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 3/4 | chr16 | 82090192 | ||||||
chr16:82090302
|
G | GT | 52 | a0000c0002t0001g0329a0000c0002t0002g0041a0000c0002t0002g0042others(49): 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 | a0000c0002t0001g0308a0001c0001t0001g0020a0001c0001t0001g0039others(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 | a0001c0001t0001g0015a0001c0001t0001g0160a0001c0001t0001g0163others(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 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0185others(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 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0289others(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 | a0001c0001t0001g0249a0001c0001t0001g0313a0001c0001t0001g0321others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0184 | 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 | 26 | a0001c0001t0001g0007a0001c0001t0001g0207a0001c0001t0001g0210others(23): 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 | 34 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0187others(31): 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 | 23 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0188others(20): Show | 24 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(21): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0171others(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 | 42 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(39): 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 | a0001c0001t0001g0242a0001c0001t0001g0282a0001c0001t0001g0283others(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 | a0001c0001t0002g0032a0002c0005t0001g0325 | 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 | a0001c0001t0001g0340a0001c0001t0002g0108 | 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 | a0001c0001t0002g0065 | 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 | a0001c0001t0002g0008a0001c0001t0002g0064a0001c0001t0002g0179 | 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 | a0001c0001t0002g0044a0001c0001t0002g0046 | 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 | 273 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(270): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | a0001c0003t0002g0131 | 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 | a0001c0001t0001g0313a0001c0001t0001g0342 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0340a0001c0001t0002g0108 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0020a0001c0001t0001g0174a0001c0001t0001g0176others(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 | a0001c0001t0001g0341 | 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 | a0001c0001t0002g0070 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.802+86C>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091125 | ||||||
chr16:82091171
|
G | T | 345 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(342): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.802+132G>T | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82091171 | ||||||
chr16:82091242
|
G | A | 1 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0012a0001c0001t0001g0218a0001c0001t0001g0219 | 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 | a0001c0001t0001g0066a0001c0001t0001g0307 | 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 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0001g0238 | 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 | a0001c0001t0002g0126 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0345 | 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 | 283 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(280): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0002g0106a0001c0001t0002g0115a0001c0001t0002g0116others(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 | 120 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(117): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(124): 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 | a0001c0001t0001g0341 | 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 | a0001c0001t0001g0056a0001c0001t0002g0096a0001c0001t0002g0106others(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 | 305 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(302): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.802+1113G>C | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82092152 | ||||||
chr16:82092179
|
C | T | 121 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(118): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(125): 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 | a0001c0001t0001g0313a0001c0001t0001g0342 | 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 | 120 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(117): Show | 127 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(124): 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0002g0045 | 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 | a0001c0001t0001g0020a0001c0001t0001g0174a0001c0001t0001g0176others(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 | 121 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(118): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(125): 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 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0115others(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 | a0001c0006t0001g0082 | 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 | a0001c0001t0001g0341 | 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 | a0001c0001t0002g0051 | 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 | a0006c0012t0002g0103 | 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 | 54 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(51): 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 | 180 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(177): 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 | 161 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(158): 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 | 124 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(121): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(127): 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 | a0001c0001t0001g0018a0001c0001t0001g0282 | 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 | a0001c0001t0001g0330 | 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 | a0001c0001t0002g0114 | 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 | 161 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(158): 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 | 304 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(301): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0016a0001c0001t0001g0272 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 162 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(159): 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 | a0001c0001t0001g0262 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0002g0128 | 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 | a0001c0001t0002g0186 | 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 | a0001c0001t0002g0182 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 14 | a0001c0001t0001g0222a0001c0001t0001g0234a0001c0001t0001g0250others(11): 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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0298 | 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 | 160 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(157): 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 | a0001c0001t0001g0007a0001c0001t0001g0173a0001c0001t0001g0309others(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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0007a0001c0001t0001g0173a0001c0001t0002g0062 | 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 | a0001c0001t0001g0020a0001c0001t0001g0174a0001c0001t0001g0176others(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 | a0001c0006t0001g0058 | 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 | a0001c0001t0001g0218a0001c0001t0001g0219 | 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 | a0001c0001t0001g0341 | 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 | 225 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(222): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): 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 | a0000c0004t0001g0152 | 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 | a0001c0001t0002g0047 | 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 | 176 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(173): 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 | 160 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(157): 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0205 | 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 | 62 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(59): Show | 64 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(61): 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 | a0001c0001t0001g0341 | 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 | a0001c0001t0001g0225 | 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 | a0001c0003t0002g0109 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0006t0001g0294 | 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 | a0001c0001t0002g0172 | 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 | 230 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(227): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): 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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | a0001c0001t0001g0060 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 66 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(63): 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 | a0001c0001t0001g0040a0001c0001t0001g0060a0001c0001t0001g0061others(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 | 166 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(163): 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 | a0001c0001t0001g0175a0001c0001t0001g0200a0001c0006t0001g0082 | 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 | a0001c0001t0001g0015a0001c0001t0001g0225a0001c0001t0001g0264others(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 | a0001c0001t0002g0059 | 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 | a0000c0004t0001g0152 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0000c0004t0001g0152 | 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 | a0001c0001t0001g0313a0001c0001t0001g0342 | 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 | a0001c0001t0001g0341 | 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 | 26 | a0001c0001t0001g0013a0001c0001t0001g0056a0001c0001t0001g0217others(23): 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 | a0001c0001t0001g0012a0001c0001t0001g0218a0001c0001t0001g0219 | 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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311 | 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 | a0001c0001t0001g0175a0001c0001t0001g0200a0001c0006t0001g0082 | 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 | a0001c0001t0001g0015a0001c0001t0001g0216a0001c0001t0001g0225others(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 | a0001c0001t0001g0313a0001c0001t0001g0342a0001c0001t0002g0126 | 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 | a0001c0001t0001g0330 | 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 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0313others(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 | 2 | a0001c0001t0002g0165a0001c0001t0002g0166 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0005c0011t0001g0228 | 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 | a0005c0011t0001g0228 | 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 | a0001c0001t0001g0209 | 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 | 22 | a0000c0002t0001g0308a0000c0002t0002g0042a0001c0001t0001g0007others(19): 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 | 159 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(156): 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 | 67 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0014others(64): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | 11 | a0001c0001t0001g0211a0001c0001t0001g0279a0001c0001t0001g0280others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.803-821C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097254 | ||||||
chr16:82097256
|
A | G | 11 | a0001c0001t0001g0211a0001c0001t0001g0279a0001c0001t0001g0280others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.803-819A>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097256 | ||||||
chr16:82097260
|
C | A | 11 | a0001c0001t0001g0211a0001c0001t0001g0279a0001c0001t0001g0280others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(8): 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 | a0001c0001t0001g0021a0001c0001t0001g0261a0001c0001t0001g0288others(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 | 16 | a0001c0001t0001g0021a0001c0001t0001g0211a0001c0001t0001g0261others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(13): 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 | a0001c0001t0001g0021a0001c0001t0001g0261a0001c0001t0001g0288others(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 | 32 | a0001c0001t0001g0016a0001c0001t0001g0192a0001c0001t0001g0201others(29): Show | 33 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.803-809C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097266 | ||||||
chr16:82097268
|
A | G | 38 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0192others(35): Show | 39 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(36): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0016a0001c0001t0001g0192a0001c0001t0001g0201others(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 | a0001c0001t0001g0341 | 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 | 11 | a0001c0001t0001g0211a0001c0001t0001g0279a0001c0001t0001g0280others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(8): 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 |
11 | a0001c0001t0001g0211a0001c0001t0001g0279a0001c0001t0001g0280others(8): Show | 11 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(8): 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 | a0001c0001t0001g0021a0001c0001t0001g0261a0001c0001t0001g0288others(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 | a0001c0001t0001g0016a0001c0001t0001g0192a0001c0001t0001g0201others(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 | 16 | a0001c0001t0001g0021a0001c0001t0001g0211a0001c0001t0001g0261others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-795G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097280 | ||||||
chr16:82097282
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0211a0001c0001t0001g0261others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-793G>A | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82097282 | ||||||
chr16:82097284
|
G | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0211a0001c0001t0001g0261others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(13): 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 | a0001c0001t0001g0016a0001c0001t0001g0192a0001c0001t0001g0201others(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 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0267others(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 | a0001c0001t0001g0341 | 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 | 39 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0056others(36): 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 | 47 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(44): 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 |
106 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(103): 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 | a0001c0001t0001g0185a0001c0001t0001g0217a0001c0001t0001g0326others(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 | a0001c0001t0001g0307a0001c0001t0002g0089a0001c0001t0002g0116others(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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0175a0001c0001t0001g0200a0001c0001t0002g0027others(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 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(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 | 37 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0187others(34): Show | 38 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(35): 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 | a0001c0001t0001g0007a0001c0001t0001g0173a0001c0001t0002g0062 | 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 | a0001c0001t0002g0034 | 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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(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 | a0001c0001t0001g0333 | 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 | a0001c0001t0001g0313a0001c0001t0001g0342 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0002g0019a0001c0001t0002g0312 | 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 | a0001c0001t0001g0341 | 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 | a0000c0002t0001g0306a0000c0002t0001g0308a0000c0002t0001g0314others(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 | a0001c0001t0001g0319 | 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 | a0001c0001t0001g0341 | 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 | a0001c0001t0002g0186 | 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 | a0001c0001t0002g0076a0001c0001t0002g0118a0001c0001t0002g0179 | 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 | 158 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(155): 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 | a0001c0001t0001g0012a0001c0001t0001g0218a0001c0001t0001g0219others(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 | 216 | a0000c0002t0002g0123a0000c0002t0002g0127a0000c0002t0002g0168others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): 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 | a0001c0001t0002g0026 | 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 | 37 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0187others(34): Show | 38 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.803-57C>G | HSD17B2 | ENSG00000086696.11 | transcript | ENST00000199936.9 | protein_coding | 4/4 | chr16 | 82098018 |