geneid | 124535 |
---|---|
ensemblid | ENSG00000176160.11 |
hgncid | 26862 |
symbol | HSF5 |
name | heat shock transcription factor 5 |
refseq_nuc | NM_001080439.3 |
refseq_prot | NP_001073908.2 |
ensembl_nuc | ENST00000323777.8 |
ensembl_prot | ENSP00000313243.3 |
mane_status | MANE Select |
chr | chr17 |
start | 58420167 |
end | 58488408 |
strand | - |
ver | v1.2 |
region | chr17:58420167-58488408 |
region5000 | chr17:58415167-58493408 |
regionname0 | HSF5_chr17_58420167_58488408 |
regionname5000 | HSF5_chr17_58415167_58493408 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 596 | 266 | 77 | 54 | 95 | 9 | 29 | 71 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0002 | 0/0 | 596 | 57 | 0 | 12 | 37 | 3 | 5 | 31 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0003 | 0/0 | 598 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0004 | 0/0 | 596 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0005 | 0/0 | 596 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0006 | 0/0 | 596 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0007 | 0/0 | 596 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0008 | 0/0 | 596 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0009 | 0/0 | 596 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1791 | 262 | 73 | 54 | 95 | 9 | 29 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0002 | 0/0 | 1791 | 57 | 0 | 12 | 37 | 3 | 5 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0003 | 0/0 | 1797 | 3 | 1 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0004 | 0/0 | 1791 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0005 | 0/0 | 1791 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0006 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0007 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0008 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0009 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0010 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
c0011 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2328 | 317 | 73 | 69 | 129 | 11 | 33 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0002 | 0/0 | 2328 | 4 | 0 | 0 | 4 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0003 | 0/0 | 2328 | 2 | 0 | 1 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0004 | 0/0 | 2328 | 2 | 0 | 0 | 0 | 0 | 2 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0005 | 0/0 | 2328 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0006 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0007 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0008 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0009 | 0/0 | 2328 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
t0010 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1791 | 262 | 73 | 54 | 95 | 9 | 29 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0004 | 0/0 | 1791 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0005 | 0/0 | 1791 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0002c0002 | 0/0 | 1791 | 57 | 0 | 12 | 37 | 3 | 5 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0003c0003 | 0/0 | 1797 | 3 | 1 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0004c0011 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0005c0009 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0006c0008 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0007c0010 | 0/0 | 1791 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0008c0007 | 0/0 | 1791 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0009c0006 | 0/0 | 1791 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4118 | 248 | 69 | 53 | 90 | 8 | 26 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0002 | 0/0 | 4118 | 4 | 0 | 0 | 4 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0003 | 0/0 | 4118 | 2 | 0 | 1 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0004 | 0/0 | 4118 | 2 | 0 | 0 | 0 | 0 | 2 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0005 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0006 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0007 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0009 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0001t0010 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0004t0001 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0001c0005t0001 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0002c0002t0001 | 0/0 | 4118 | 57 | 0 | 12 | 37 | 3 | 5 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0003c0003t0001 | 0/0 | 4124 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0003c0003t0008 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0004c0011t0001 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0005c0009t0001 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0006c0008t0001 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0007c0010t0001 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0008c0007t0001 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
a0009c0006t0001 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | copy fasta | chr17 | 58415167 | 58493408 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0003c0003t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0004c0011t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0005c0009t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0006c0008t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0007c0010t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0008c0007t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
a0009c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0254 | EUR | GBR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0253 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0307 | EUR | FIN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01257 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01261 | hp2 | a0008 | c0007 | t0001 | g0197 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0273 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01358 | hp1 | a0005 | c0009 | t0001 | g0130 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0237 | EUR | IBS | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0069 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0073 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03017 | hp1 | a0004 | c0011 | t0001 | g0230 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03654 | hp1 | a0009 | c0006 | t0001 | g0224 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0238 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0184 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0321 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0196 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0271 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0169 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18980 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19007 | hp1 | a0007 | c0010 | t0001 | g0044 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19083 | hp1 | a0006 | c0008 | t0001 | g0067 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0319 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20129 | hp2 | a0003 | c0003 | t0008 | g0322 | AFR | ASW | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0244 | SAS | GIH | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | GIH | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0153 | REF | REF | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | HSF5_chr17_58415167_58493408 | HSF5 | chr17 | 58415167 | 58493408 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:58458785
|
T | G | 1 | a0006 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.1703A>C | p.Gln568Pro | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/6 | 1837/4118 | 1703/1791 | 568/596 | chr17 | 58458785 | ||
chr17:58458896
|
G | A | 1 | a0005 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1592C>T | p.Pro531Leu | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/6 | 1726/4118 | 1592/1791 | 531/596 | chr17 | 58458896 | ||
chr17:58458933
|
T | C | 1 | a0007 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.1555A>G | p.Ile519Val | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/6 | 1689/4118 | 1555/1791 | 519/596 | chr17 | 58458933 | ||
chr17:58462785
|
G | T | 1 | a0008 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1539C>A | p.His513Gln | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/6 | 1673/4118 | 1539/1791 | 513/596 | chr17 | 58462785 | ||
chr17:58462906
|
C | T | 3 | a0002a0004a0009 | 59 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(56): Show |
missense_variant | MODERATE | c.1418G>A | p.Ser473Asn | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/6 | 1552/4118 | 1418/1791 | 473/596 | chr17 | 58462906 | ||
chr17:58480000
|
G | A | 1 | a0004 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.818C>T | p.Thr273Ile | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/6 | 952/4118 | 818/1791 | 273/596 | chr17 | 58480000 | ||
chr17:58480184
|
C | T | 1 | a0009 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.634G>A | p.Asp212Asn | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/6 | 768/4118 | 634/1791 | 212/596 | chr17 | 58480184 | ||
chr17:58488072
|
T | TCGGCCC | 1 | a0003 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
conservative_inframe_insertion | MODERATE | c.197_202dupGGGCCG | p.Gly66_Ala67dup | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/6 | 336/4118 | 202/1791 | 68/596 | chr17 | 58488072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:58466906
|
A | G | 1 | a0001c0004 | 2 | NA18906.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.999T>C | p.Tyr333Tyr | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/6 | 1133/4118 | 999/1791 | 333/596 | chr17 | 58466906 | ||
chr17:58480020
|
G | A | 1 | a0001c0005 | 2 | HG02895.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.798C>T | p.Thr266Thr | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/6 | 932/4118 | 798/1791 | 266/596 | chr17 | 58480020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:58420358
|
T | C | 1 | a0003c0003t0008 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2002A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 2002 | chr17 | 58420358 | |||||
chr17:58420528
|
T | C | 1 | a0001c0001t0004 | 2 | HG04184.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1832 | chr17 | 58420528 | |||||
chr17:58420559
|
T | C | 1 | a0001c0001t0009 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1801 | chr17 | 58420559 | |||||
chr17:58420600
|
T | A | 1 | a0001c0001t0010 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1760 | chr17 | 58420600 | |||||
chr17:58421027
|
G | A | 1 | a0001c0001t0002 | 4 | NA18939.hp2 NA18954.hp1 NA19000.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1333C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 1333 | chr17 | 58421027 | |||||
chr17:58421669
|
C | T | 1 | a0001c0001t0003 | 2 | HG00323.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*691G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 691 | chr17 | 58421669 | |||||
chr17:58422160
|
G | C | 1 | a0001c0001t0005 | 2 | HG02451.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 200 | chr17 | 58422160 | |||||
chr17:58422311
|
C | T | 1 | a0001c0001t0007 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 6/6 | 49 | chr17 | 58422311 | |||||
chr17:58488277
|
C | T | 1 | a0001c0001t0006 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/6 | 3 | chr17 | 58488277 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:58422471
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0107others(3): Show | 7 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-41A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422471 | ||||||
chr17:58422481
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1721-51A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422481 | ||||||
chr17:58422688
|
A | C | 3 | a0002c0002t0001g0228a0002c0002t0001g0262a0002c0002t0001g0265 | 3 | NA18612.hp2 NA18939.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1721-258T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422688 | ||||||
chr17:58422694
|
CT | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1721-265delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422694 | ||||||
chr17:58422694
|
CTT | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0045others(7): Show | 10 | HG00558.hp1 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1721-266_1721-265d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422694 | ||||||
chr17:58422718
|
G | A | 1 | a0001c0001t0010g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1721-288C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422718 | ||||||
chr17:58422735
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1721-305C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422735 | ||||||
chr17:58422798
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-368A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422798 | ||||||
chr17:58422856
|
C | T | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-426G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58422856 | ||||||
chr17:58423101
|
T | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305 | 3 | HG00642.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1721-671A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423101 | ||||||
chr17:58423275
|
A | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0298a0001c0001t0010g0014 | 3 | HG02257.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1721-845T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423275 | ||||||
chr17:58423290
|
G | A | 2 | a0001c0001t0004g0196a0001c0001t0004g0212 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1721-860C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423290 | ||||||
chr17:58423291
|
GTTCA | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 7 | HG02055.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1721-865_1721-862d others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423291 | ||||||
chr17:58423483
|
C | CT | 74 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0021others(71): Show | 76 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1721-1054dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423483 | ||||||
chr17:58423483
|
CT | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(7): Show | 12 | HG01070.hp1 HG01081.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1721-1054delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423483 | ||||||
chr17:58423537
|
G | A | 69 | a0001c0001t0001g0008a0001c0001t0001g0080a0001c0001t0001g0153others(66): Show | 71 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1721-1107C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423537 | ||||||
chr17:58423570
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-1140G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423570 | ||||||
chr17:58423608
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-1178A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423608 | ||||||
chr17:58423653
|
A | G | 5 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0181others(2): Show | 5 | HG00099.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-1223T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423653 | ||||||
chr17:58423775
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1721-1345C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423775 | ||||||
chr17:58423893
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0111 | 2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1721-1463G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58423893 | ||||||
chr17:58424051
|
C | T | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-1621G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424051 | ||||||
chr17:58424059
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1721-1629T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424059 | ||||||
chr17:58424120
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1721-1690T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424120 | ||||||
chr17:58424189
|
ACAGCAGT others(5): Show |
A | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1721-1771_1721-176 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424189 | ||||||
chr17:58424387
|
CA | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1721-1958delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424387 | ||||||
chr17:58424611
|
C | CA | 10 | a0001c0001t0001g0032a0001c0001t0001g0096a0001c0001t0001g0124others(7): Show | 10 | HG01109.hp1 HG02451.hp2 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-2182dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424611 | ||||||
chr17:58424611
|
CA | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0280a0001c0001t0001g0282others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-2182delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424611 | ||||||
chr17:58424903
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(23): Show | 29 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1721-2473G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58424903 | ||||||
chr17:58425406
|
TA | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1721-2977delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425406 | ||||||
chr17:58425575
|
C | CA | 87 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0051others(84): Show | 88 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1721-3146dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | ||||||
chr17:58425575
|
C | CAA | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0031others(14): Show | 19 | HG00544.hp1 HG00642.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.1721-3147_1721-314 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | ||||||
chr17:58425575
|
C | CAAAA | 15 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 16 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1721-3149_1721-314 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | ||||||
chr17:58425575
|
CA | C | 11 | a0001c0001t0001g0094a0001c0001t0001g0158a0001c0001t0001g0187others(8): Show | 11 | HG01169.hp1 HG01255.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1721-3146delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | ||||||
chr17:58425575
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-3155_1721-314 others(14): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425575 | ||||||
chr17:58425590
|
A | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0085others(10): Show | 13 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1721-3160T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425590 | ||||||
chr17:58425974
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1721-3544T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58425974 | ||||||
chr17:58426373
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1721-3943A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58426373 | ||||||
chr17:58426973
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1721-4543G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58426973 | ||||||
chr17:58427129
|
T | C | 3 | a0001c0001t0001g0093a0001c0005t0001g0069a0001c0005t0001g0073 | 3 | HG02559.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1721-4699A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427129 | ||||||
chr17:58427292
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1721-4862T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427292 | ||||||
chr17:58427512
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1721-5082C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427512 | ||||||
chr17:58427868
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1721-5438C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427868 | ||||||
chr17:58427932
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-5502G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58427932 | ||||||
chr17:58428165
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-5735G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428165 | ||||||
chr17:58428202
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1721-5772G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428202 | ||||||
chr17:58428402
|
G | GT | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-5973dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428402 | ||||||
chr17:58428444
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1721-6014C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428444 | ||||||
chr17:58428448
|
A | G | 1 | a0002c0002t0001g0272 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1721-6018T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428448 | ||||||
chr17:58428590
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1721-6160G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428590 | ||||||
chr17:58428602
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1721-6172A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428602 | ||||||
chr17:58428752
|
G | A | 1 | a0002c0002t0001g0278 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1721-6322C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428752 | ||||||
chr17:58428799
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 118 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1721-6369T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428799 | ||||||
chr17:58428976
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-6546A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58428976 | ||||||
chr17:58429124
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1721-6694C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429124 | ||||||
chr17:58429273
|
G | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1721-6843C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429273 | ||||||
chr17:58429482
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1721-7052G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429482 | ||||||
chr17:58429500
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1721-7070G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429500 | ||||||
chr17:58429702
|
C | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1721-7272G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429702 | ||||||
chr17:58429719
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1721-7289C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429719 | ||||||
chr17:58429756
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1721-7326C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429756 | ||||||
chr17:58429842
|
T | TA | 69 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0051others(66): Show | 71 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1721-7413dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429842 | ||||||
chr17:58429842
|
T | TAAA | 20 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(17): Show | 22 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1721-7415_1721-741 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429842 | ||||||
chr17:58429842
|
TA | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1721-7413delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58429842 | ||||||
chr17:58430058
|
C | T | 3 | a0002c0002t0001g0050a0002c0002t0001g0264a0002c0002t0001g0272 | 3 | HG02071.hp1 NA18943.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1721-7628G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58430058 | ||||||
chr17:58430178
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0175 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1721-7748T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58430178 | ||||||
chr17:58430584
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1721-8154C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58430584 | ||||||
chr17:58431055
|
A | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-8625T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431055 | ||||||
chr17:58431285
|
G | T | 1 | a0002c0002t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1721-8855C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431285 | ||||||
chr17:58431412
|
A | C | 5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0164others(2): Show | 5 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1721-8982T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431412 | ||||||
chr17:58431449
|
T | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-9019A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431449 | ||||||
chr17:58431547
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1721-9117C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431547 | ||||||
chr17:58431602
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1721-9172T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431602 | ||||||
chr17:58431608
|
A | G | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-9178T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58431608 | ||||||
chr17:58432036
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0046 | 3 | NA18946.hp2 NA18964.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1721-9606G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432036 | ||||||
chr17:58432106
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1721-9676A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432106 | ||||||
chr17:58432202
|
T | G | 1 | a0001c0001t0001g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1721-9772A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432202 | ||||||
chr17:58432263
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1721-9833G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432263 | ||||||
chr17:58432504
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(23): Show | 29 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1721-10074G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432504 | ||||||
chr17:58432779
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0001t0001g0229others(65): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1721-10349T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432779 | ||||||
chr17:58432898
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1721-10468A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432898 | ||||||
chr17:58432944
|
G | A | 58 | a0001c0001t0001g0153a0002c0002t0001g0007a0002c0002t0001g0050others(55): Show | 59 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1721-10514C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432944 | ||||||
chr17:58432998
|
C | CCATT | 75 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1721-10572_1721-10 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432998 | ||||||
chr17:58432998
|
C | CCATTCAT others(5): Show |
2 | a0001c0005t0001g0069a0001c0005t0001g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1721-10580_1721-10 others(18): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432998 | ||||||
chr17:58432998
|
CCATT | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0064others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1721-10572_1721-10 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58432998 | ||||||
chr17:58433426
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0213 | 2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1721-10996A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433426 | ||||||
chr17:58433602
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1721-11172A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433602 | ||||||
chr17:58433746
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-11316C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433746 | ||||||
chr17:58433875
|
A | G | 1 | a0002c0002t0001g0271 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1721-11445T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433875 | ||||||
chr17:58433911
|
A | AT | 7 | a0001c0001t0001g0084a0001c0001t0001g0096a0001c0001t0001g0133others(4): Show | 7 | HG00544.hp2 HG01981.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-11482dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | ||||||
chr17:58433911
|
A | ATTTTTTT others(1): Show |
28 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(25): Show | 31 | HG00323.hp1 HG00735.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1721-11489_1721-11 others(14): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | ||||||
chr17:58433911
|
A | ATTTTTTT others(2): Show |
129 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0026others(126): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1721-11490_1721-11 others(15): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | ||||||
chr17:58433911
|
A | ATTTTTTT others(3): Show |
38 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0042others(35): Show | 39 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1721-11491_1721-11 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | ||||||
chr17:58433911
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0180a0001c0001t0001g0215a0002c0002t0001g0225 | 3 | NA18994.hp2 NA18999.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1721-11492_1721-11 others(17): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433911 | ||||||
chr17:58433986
|
T | TCAGTGCA others(5): Show |
1 | a0001c0001t0001g0215 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1721-11568_1721-11 others(18): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58433986 | ||||||
chr17:58434102
|
G | A | 1 | a0007c0010t0001g0044 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1721-11672C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434102 | ||||||
chr17:58434102
|
G | T | 1 | a0001c0001t0001g0002 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1721-11672C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434102 | ||||||
chr17:58434189
|
A | G | 1 | a0002c0002t0001g0251 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1721-11759T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434189 | ||||||
chr17:58434300
|
G | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-11870C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434300 | ||||||
chr17:58434418
|
G | A | 1 | a0002c0002t0001g0262 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1721-11988C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434418 | ||||||
chr17:58434420
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1721-11990C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434420 | ||||||
chr17:58434544
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-12114G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434544 | ||||||
chr17:58434549
|
CA | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0121others(5): Show | 8 | HG00558.hp2 HG00642.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1721-12120delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434549 | ||||||
chr17:58434563
|
A | G | 61 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 61 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1721-12133T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434563 | ||||||
chr17:58434725
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1721-12295C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434725 | ||||||
chr17:58434844
|
C | T | 2 | a0002c0002t0001g0050a0002c0002t0001g0264 | 2 | HG02071.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1721-12414G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434844 | ||||||
chr17:58434875
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1721-12445A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434875 | ||||||
chr17:58434956
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0163a0001c0001t0001g0316 | 4 | NA18946.hp1 NA18993.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-12526A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58434956 | ||||||
chr17:58435264
|
T | C | 1 | a0002c0002t0001g0189 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1721-12834A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435264 | ||||||
chr17:58435270
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1721-12840C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435270 | ||||||
chr17:58435741
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1721-13311A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435741 | ||||||
chr17:58435758
|
G | A | 1 | a0006c0008t0001g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1721-13328C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435758 | ||||||
chr17:58435791
|
C | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-13361G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435791 | ||||||
chr17:58435794
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0286others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-13364C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435794 | ||||||
chr17:58435832
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-13402C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435832 | ||||||
chr17:58435898
|
C | CA | 103 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(100): Show | 105 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1721-13469dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58435898 | ||||||
chr17:58436345
|
CT | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(24): Show | 30 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1721-13916delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436345 | ||||||
chr17:58436498
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00639.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1721-14068T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436498 | ||||||
chr17:58436504
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14074A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436504 | ||||||
chr17:58436536
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14106A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436536 | ||||||
chr17:58436735
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14305G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436735 | ||||||
chr17:58436840
|
T | C | 4 | a0002c0002t0001g0225a0002c0002t0001g0263a0002c0002t0001g0276others(1): Show | 4 | NA18997.hp1 NA19064.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-14410A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436840 | ||||||
chr17:58436840
|
T | TAAC | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-14413_1721-14 others(9): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436840 | ||||||
chr17:58436932
|
AC | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(95): Show | 99 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1721-14503delG | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58436932 | ||||||
chr17:58437097
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(95): Show | 99 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1721-14667C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58437097 | ||||||
chr17:58437927
|
G | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0308 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1721-15497C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58437927 | ||||||
chr17:58438029
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1721-15599A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438029 | ||||||
chr17:58438213
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1721-15783T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438213 | ||||||
chr17:58438249
|
C | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-15819G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438249 | ||||||
chr17:58438358
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1721-15928T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438358 | ||||||
chr17:58438671
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1721-16241T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438671 | ||||||
chr17:58438814
|
T | C | 6 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(3): Show | 6 | HG00642.hp1 HG03704.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-16384A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438814 | ||||||
chr17:58438816
|
GCACTAAG others(6): Show |
G | 6 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(3): Show | 6 | HG00642.hp1 HG03704.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1721-16399_1721-16 others(19): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438816 | ||||||
chr17:58438885
|
G | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0097others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-16455C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438885 | ||||||
chr17:58438894
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1721-16464T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438894 | ||||||
chr17:58438976
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1721-16546T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58438976 | ||||||
chr17:58439126
|
CA | C | 13 | a0002c0002t0001g0171a0002c0002t0001g0226a0002c0002t0001g0227others(10): Show | 13 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.1721-16697delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439126 | ||||||
chr17:58439134
|
A | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-16704T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439134 | ||||||
chr17:58439275
|
A | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1721-16845T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439275 | ||||||
chr17:58439284
|
A | AAAC | 26 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(23): Show | 29 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1721-16857_1721-16 others(9): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439284 | ||||||
chr17:58439333
|
ACATATGT others(11): Show |
A | 2 | a0001c0001t0001g0103a0001c0001t0001g0106 | 2 | HG01168.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1721-16921_1721-16 others(24): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439333 | ||||||
chr17:58439447
|
C | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0193a0001c0001t0001g0202others(1): Show | 4 | NA18994.hp2 NA19001.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-17017G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439447 | ||||||
chr17:58439471
|
A | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1721-17041T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439471 | ||||||
chr17:58439506
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0209 | 2 | HG00099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1721-17076G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439506 | ||||||
chr17:58439673
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0035others(169): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1721-17243C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439673 | ||||||
chr17:58439727
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1721-17297C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58439727 | ||||||
chr17:58440130
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-17700C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440130 | ||||||
chr17:58440417
|
T | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0216others(2): Show | 5 | HG02257.hp1 HG02293.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-17987A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440417 | ||||||
chr17:58440601
|
G | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1720+18167C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440601 | ||||||
chr17:58440767
|
C | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+18001G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440767 | ||||||
chr17:58440937
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1720+17831C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440937 | ||||||
chr17:58440940
|
T | TA | 19 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+17827dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58440940 | ||||||
chr17:58441015
|
CAGAT | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+17749_1720+17 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58441015 | ||||||
chr17:58441173
|
T | G | 6 | a0001c0001t0001g0187a0001c0001t0001g0206a0001c0001t0001g0210others(3): Show | 6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+17595A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58441173 | ||||||
chr17:58441844
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1720+16924C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58441844 | ||||||
chr17:58442130
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1720+16638C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442130 | ||||||
chr17:58442267
|
C | G | 1 | a0009c0006t0001g0224 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1720+16501G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442267 | ||||||
chr17:58442379
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1720+16389C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442379 | ||||||
chr17:58442675
|
C | A | 69 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0001t0001g0229others(66): Show | 71 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1720+16093G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442675 | ||||||
chr17:58442713
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+16055T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442713 | ||||||
chr17:58442716
|
CTTAG | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0286others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+16048_1720+16 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442716 | ||||||
chr17:58442766
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1720+16002A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442766 | ||||||
chr17:58442789
|
G | A | 1 | a0002c0002t0001g0276 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1720+15979C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442789 | ||||||
chr17:58442862
|
T | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0298 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1720+15906A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442862 | ||||||
chr17:58442873
|
G | C | 19 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+15895C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442873 | ||||||
chr17:58442912
|
A | AT | 26 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(23): Show | 28 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1720+15855dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442912 | ||||||
chr17:58442987
|
C | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+15781G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58442987 | ||||||
chr17:58443065
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 117 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1720+15703C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443065 | ||||||
chr17:58443098
|
G | A | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+15670C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443098 | ||||||
chr17:58443164
|
C | A | 4 | a0002c0002t0001g0171a0002c0002t0001g0249a0002c0002t0001g0259others(1): Show | 4 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+15604G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443164 | ||||||
chr17:58443227
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1720+15541G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443227 | ||||||
chr17:58443234
|
T | C | 7 | a0002c0002t0001g0237a0002c0002t0001g0241a0002c0002t0001g0245others(4): Show | 7 | HG00733.hp1 HG01099.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+15534A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443234 | ||||||
chr17:58443284
|
A | AGT | 5 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0216others(2): Show | 5 | HG02257.hp1 HG02293.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+15483_1720+15 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443284 | ||||||
chr17:58443737
|
C | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+15031G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443737 | ||||||
chr17:58443768
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 16 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1720+15000G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443768 | ||||||
chr17:58443828
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1720+14940A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443828 | ||||||
chr17:58443882
|
G | A | 3 | a0002c0002t0001g0228a0002c0002t0001g0262a0002c0002t0001g0265 | 3 | NA18612.hp2 NA18939.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1720+14886C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443882 | ||||||
chr17:58443927
|
G | A | 1 | a0002c0002t0001g0231 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1720+14841C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443927 | ||||||
chr17:58443946
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1720+14822C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58443946 | ||||||
chr17:58444023
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14745G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444023 | ||||||
chr17:58444030
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0020 | 2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1720+14738C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444030 | ||||||
chr17:58444097
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1720+14671A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444097 | ||||||
chr17:58444498
|
GA | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14269delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444498 | ||||||
chr17:58444649
|
T | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14119A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444649 | ||||||
chr17:58444657
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1720+14111G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444657 | ||||||
chr17:58444676
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+14092C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58444676 | ||||||
chr17:58445022
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1720+13746T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445022 | ||||||
chr17:58445082
|
C | T | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+13686G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445082 | ||||||
chr17:58445172
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1720+13596T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445172 | ||||||
chr17:58445474
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1720+13294A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445474 | ||||||
chr17:58445618
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1720+13150A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445618 | ||||||
chr17:58445721
|
G | C | 5 | a0002c0002t0001g0062a0002c0002t0001g0238a0002c0002t0001g0243others(2): Show | 5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+13047C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445721 | ||||||
chr17:58445816
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0266others(5): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+12952T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445816 | ||||||
chr17:58445927
|
G | A | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+12841C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445927 | ||||||
chr17:58445942
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1720+12826G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58445942 | ||||||
chr17:58446137
|
C | CA | 13 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(10): Show | 14 | HG00438.hp2 HG01175.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+12630dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446137 | ||||||
chr17:58446137
|
CA | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0063a0001c0001t0001g0179others(3): Show | 6 | HG01256.hp2 HG01515.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+12630delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446137 | ||||||
chr17:58446157
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+12611C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446157 | ||||||
chr17:58446158
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1720+12610C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446158 | ||||||
chr17:58446186
|
C | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+12582G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446186 | ||||||
chr17:58446288
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+12480G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446288 | ||||||
chr17:58446433
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1720+12335A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446433 | ||||||
chr17:58446442
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+12326A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446442 | ||||||
chr17:58446539
|
G | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 20 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+12229C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446539 | ||||||
chr17:58446644
|
G | A | 6 | a0001c0001t0001g0187a0001c0001t0001g0206a0001c0001t0001g0210others(3): Show | 6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+12124C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446644 | ||||||
chr17:58446849
|
A | G | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+11919T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446849 | ||||||
chr17:58446941
|
A | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+11827T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446941 | ||||||
chr17:58446945
|
T | C | 86 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1720+11823A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58446945 | ||||||
chr17:58447040
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+11728C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447040 | ||||||
chr17:58447070
|
AGCCAAGA others(4): Show |
A | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+11687_1720+11 others(17): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447070 | ||||||
chr17:58447368
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1720+11400C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447368 | ||||||
chr17:58447620
|
G | A | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+11148C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58447620 | ||||||
chr17:58448078
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+10690C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448078 | ||||||
chr17:58448133
|
C | CA | 18 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0080others(15): Show | 18 | HG01070.hp1 HG01081.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.1720+10634dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448133 | ||||||
chr17:58448133
|
CA | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(109): Show | 117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1720+10634delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448133 | ||||||
chr17:58448133
|
CAA | C | 79 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(76): Show | 79 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1720+10633_1720+10 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448133 | ||||||
chr17:58448375
|
T | G | 1 | a0002c0002t0001g0246 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1720+10393A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448375 | ||||||
chr17:58448428
|
A | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+10340T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448428 | ||||||
chr17:58448705
|
C | T | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+10063G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448705 | ||||||
chr17:58448735
|
GCAA | G | 23 | a0002c0002t0001g0062a0002c0002t0001g0189a0002c0002t0001g0237others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1720+10030_1720+10 others(9): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448735 | ||||||
chr17:58448791
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1720+9977T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58448791 | ||||||
chr17:58449466
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+9302C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449466 | ||||||
chr17:58449689
|
G | A | 5 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0216others(2): Show | 5 | HG02257.hp1 HG02293.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+9079C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449689 | ||||||
chr17:58449697
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1720+9071G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449697 | ||||||
chr17:58449699
|
CA | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 106 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1720+9068delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449699 | ||||||
chr17:58449715
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 8 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1720+9053T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449715 | ||||||
chr17:58449751
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1720+9017G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449751 | ||||||
chr17:58449756
|
G | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1720+9012C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449756 | ||||||
chr17:58449795
|
G | A | 1 | a0001c0001t0010g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1720+8973C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449795 | ||||||
chr17:58449820
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1720+8948C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449820 | ||||||
chr17:58449839
|
C | T | 6 | a0001c0001t0001g0187a0001c0001t0001g0206a0001c0001t0001g0210others(3): Show | 6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+8929G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449839 | ||||||
chr17:58449939
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1720+8829G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449939 | ||||||
chr17:58449954
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+8814G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58449954 | ||||||
chr17:58450022
|
C | CA | 33 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(30): Show | 34 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1720+8745dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450022 | ||||||
chr17:58450022
|
CAAAAAAA others(1): Show |
C | 66 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(63): Show | 68 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1720+8738_1720+874 others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450022 | ||||||
chr17:58450208
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+8560C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450208 | ||||||
chr17:58450261
|
C | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0155 | 3 | HG02004.hp1 HG02273.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1720+8507G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450261 | ||||||
chr17:58450295
|
CGCCATTG others(3249): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1720+5217_1720+847 others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450295 | ||||||
chr17:58450337
|
T | C | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1720+8431A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450337 | ||||||
chr17:58450338
|
C | CA | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(17): Show | 22 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.1720+8429dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450338 | ||||||
chr17:58450338
|
CA | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(128): Show | 137 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1720+8429delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450338 | ||||||
chr17:58450443
|
A | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+8325T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450443 | ||||||
chr17:58450644
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+8124A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450644 | ||||||
chr17:58450740
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 5 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+8028G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450740 | ||||||
chr17:58450753
|
C | CA | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1720+8014dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450753 | ||||||
chr17:58450994
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1720+7774G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58450994 | ||||||
chr17:58451003
|
C | T | 1 | a0005c0009t0001g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1720+7765G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451003 | ||||||
chr17:58451106
|
T | C | 27 | a0002c0002t0001g0050a0002c0002t0001g0171a0002c0002t0001g0225others(24): Show | 27 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.1720+7662A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451106 | ||||||
chr17:58451109
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0266others(5): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+7659G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451109 | ||||||
chr17:58451536
|
C | T | 1 | a0002c0002t0001g0271 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1720+7232G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451536 | ||||||
chr17:58451600
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1720+7168C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451600 | ||||||
chr17:58451819
|
A | G | 1 | a0002c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1720+6949T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451819 | ||||||
chr17:58451948
|
T | TA | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1720+6819dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451948 | ||||||
chr17:58451948
|
T | TAA | 92 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(89): Show | 93 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1720+6818_1720+681 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451948 | ||||||
chr17:58451973
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+6795G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58451973 | ||||||
chr17:58452092
|
T | A | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+6676A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452092 | ||||||
chr17:58452138
|
A | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+6630T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452138 | ||||||
chr17:58452198
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1720+6570A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452198 | ||||||
chr17:58452412
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1720+6356A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452412 | ||||||
chr17:58452480
|
C | T | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1720+6288G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452480 | ||||||
chr17:58452622
|
C | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+6146G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452622 | ||||||
chr17:58452738
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+6030C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452738 | ||||||
chr17:58452875
|
TA | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1720+5892delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58452875 | ||||||
chr17:58453236
|
C | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0015others(27): Show | 33 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1720+5532G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453236 | ||||||
chr17:58453386
|
G | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+5382C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453386 | ||||||
chr17:58453576
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1720+5192G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453576 | ||||||
chr17:58453599
|
A | AAAC | 19 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0056others(16): Show | 19 | HG00544.hp2 HG01255.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1720+5166_1720+516 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453599 | ||||||
chr17:58453599
|
A | AAACAAC | 19 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(16): Show | 20 | HG00735.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+5163_1720+516 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453599 | ||||||
chr17:58453599
|
AAAC | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 7 | HG01257.hp1 HG01258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+5166_1720+516 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453599 | ||||||
chr17:58453707
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+5061T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453707 | ||||||
chr17:58453880
|
G | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0298 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1720+4888C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453880 | ||||||
chr17:58453916
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1720+4852C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453916 | ||||||
chr17:58453952
|
G | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(94): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1720+4816C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453952 | ||||||
chr17:58453964
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1720+4804G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58453964 | ||||||
chr17:58454241
|
A | C | 2 | a0001c0001t0003g0098a0001c0001t0003g0307 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1720+4527T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58454241 | ||||||
chr17:58454258
|
A | T | 1 | a0004c0011t0001g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1720+4510T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58454258 | ||||||
chr17:58454833
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1720+3935T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58454833 | ||||||
chr17:58455049
|
A | G | 1 | a0005c0009t0001g0130 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1720+3719T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455049 | ||||||
chr17:58455327
|
C | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1720+3441G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455327 | ||||||
chr17:58455397
|
G | C | 1 | a0008c0007t0001g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1720+3371C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455397 | ||||||
chr17:58455418
|
C | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0111 | 2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1720+3350G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455418 | ||||||
chr17:58455536
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1720+3232T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455536 | ||||||
chr17:58455596
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1720+3172G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455596 | ||||||
chr17:58455709
|
A | C | 1 | a0002c0002t0001g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1720+3059T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455709 | ||||||
chr17:58455874
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1720+2894C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455874 | ||||||
chr17:58455926
|
G | T | 1 | a0002c0002t0001g0240 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1720+2842C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455926 | ||||||
chr17:58455927
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1720+2841A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58455927 | ||||||
chr17:58456127
|
ATATG | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1720+2637_1720+264 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456127 | ||||||
chr17:58456129
|
A | G | 2 | a0001c0005t0001g0069a0001c0005t0001g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1720+2639T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456129 | ||||||
chr17:58456141
|
A | G | 6 | a0001c0001t0001g0187a0001c0001t0001g0206a0001c0001t0001g0210others(3): Show | 6 | HG01255.hp2 HG01261.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+2627T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456141 | ||||||
chr17:58456151
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0176 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1720+2617T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456151 | ||||||
chr17:58456153
|
G | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(8): Show | 12 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1720+2615C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456153 | ||||||
chr17:58456161
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0176 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1720+2607C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456161 | ||||||
chr17:58456161
|
GTA | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0056others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.1720+2605_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456161 | ||||||
chr17:58456163
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 10 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1720+2605T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456163 | ||||||
chr17:58456164
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0176a0001c0001t0001g0281 | 3 | HG02559.hp1 HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1720+2604A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456164 | ||||||
chr17:58456164
|
T | TAC | 67 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(64): Show | 67 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1720+2603_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456164 | ||||||
chr17:58456164
|
TATAC | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0075others(3): Show | 6 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+2600_1720+260 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456164 | ||||||
chr17:58456166
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(92): Show | 96 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1720+2602A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | ||||||
chr17:58456166
|
T | TAC | 11 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0104others(8): Show | 12 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1720+2600_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | ||||||
chr17:58456166
|
T | TACACAC | 4 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0317others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+2596_1720+260 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | ||||||
chr17:58456166
|
TAC | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0051others(57): Show | 62 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1720+2600_1720+260 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | ||||||
chr17:58456166
|
TACAC | T | 3 | a0001c0001t0001g0267a0002c0002t0001g0251a0002c0002t0001g0264 | 3 | HG02071.hp1 HG02135.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1720+2598_1720+260 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | ||||||
chr17:58456166
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0010g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1720+2590_1720+260 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456166 | ||||||
chr17:58456168
|
C | T | 1 | a0002c0002t0001g0189 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1720+2600G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456168 | ||||||
chr17:58456199
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+2569C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456199 | ||||||
chr17:58456433
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1720+2335C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456433 | ||||||
chr17:58456644
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+2124A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456644 | ||||||
chr17:58456803
|
T | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1720+1965A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456803 | ||||||
chr17:58456895
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+1873C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58456895 | ||||||
chr17:58457048
|
CA | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(65): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1720+1719delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457048 | ||||||
chr17:58457269
|
A | T | 4 | a0001c0001t0001g0154a0002c0002t0001g0007a0002c0002t0001g0252others(1): Show | 5 | HG01496.hp1 NA18945.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+1499T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457269 | ||||||
chr17:58457272
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0058others(5): Show | 10 | HG01192.hp2 HG01243.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1720+1496A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457272 | ||||||
chr17:58457424
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1720+1344G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58457424 | ||||||
chr17:58458005
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0286 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1720+763G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458005 | ||||||
chr17:58458328
|
C | A | 1 | a0001c0001t0001g0283 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1720+440G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458328 | ||||||
chr17:58458571
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1720+197T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458571 | ||||||
chr17:58458606
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1720+162T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458606 | ||||||
chr17:58458661
|
C | T | 1 | a0002c0002t0001g0252 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1720+107G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | 58458661 | ||||||
chr17:58459166
|
T | C | 1 | a0001c0001t0003g0307 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1543-221A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459166 | ||||||
chr17:58459646
|
C | CA | 88 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(85): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1543-702dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459646 | ||||||
chr17:58459664
|
G | T | 2 | a0002c0002t0001g0238a0002c0002t0001g0240 | 2 | HG03831.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1543-719C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459664 | ||||||
chr17:58459740
|
G | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-795C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459740 | ||||||
chr17:58459848
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1543-903G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58459848 | ||||||
chr17:58460212
|
TCTCA | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-1271_1543-126 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460212 | ||||||
chr17:58460354
|
G | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0164others(2): Show | 5 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1543-1409C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460354 | ||||||
chr17:58460374
|
A | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1543-1429T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460374 | ||||||
chr17:58460470
|
C | CAT | 5 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 6 | HG01243.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1543-1527_1543-152 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460470 | ||||||
chr17:58460470
|
CAT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(9): Show | 13 | HG00741.hp1 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1543-1527_1543-152 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460470 | ||||||
chr17:58460476
|
T | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0092a0002c0002t0001g0050others(7): Show | 10 | HG00323.hp1 HG02071.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543-1531A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460476 | ||||||
chr17:58460478
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1543-1533A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460478 | ||||||
chr17:58460510
|
C | CACACACA others(1): Show |
8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0035others(5): Show | 8 | HG01496.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1543-1566_1543-156 others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | ||||||
chr17:58460510
|
C | CACACAT | 32 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(29): Show | 34 | HG00323.hp1 HG00544.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1543-1566_1543-156 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | ||||||
chr17:58460510
|
C | CACAT | 85 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0029others(82): Show | 87 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1543-1566_1543-156 others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | ||||||
chr17:58460510
|
C | CAT | 107 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0030others(104): Show | 109 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1543-1567_1543-156 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | ||||||
chr17:58460510
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0046others(78): Show | 84 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1543-1565G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460510 | ||||||
chr17:58460514
|
C | A | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-1569G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460514 | ||||||
chr17:58460515
|
T | C | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1543-1570A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460515 | ||||||
chr17:58460715
|
TAA | T | 21 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1543-1772_1543-177 others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460715 | ||||||
chr17:58460755
|
C | T | 2 | a0001c0005t0001g0069a0001c0005t0001g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1543-1810G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58460755 | ||||||
chr17:58461189
|
G | A | 1 | a0001c0001t0006g0011 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1542+1593C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461189 | ||||||
chr17:58461202
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1542+1580T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461202 | ||||||
chr17:58461213
|
CACA | C | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0083others(10): Show | 14 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1542+1566_1542+156 others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | ||||||
chr17:58461213
|
CACAACA | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 188 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.1542+1563_1542+156 others(10): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | ||||||
chr17:58461213
|
CACAACAA others(2): Show |
C | 81 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0078others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1542+1560_1542+156 others(13): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | ||||||
chr17:58461213
|
CACAACAA others(5): Show |
C | 20 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0022others(17): Show | 22 | HG00438.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1542+1557_1542+156 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | ||||||
chr17:58461213
|
CACAACAA others(8): Show |
C | 8 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542+1554_1542+156 others(19): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | ||||||
chr17:58461213
|
CACAACAA others(11): Show |
C | 15 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 16 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542+1551_1542+156 others(22): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461213 | ||||||
chr17:58461278
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(65): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1542+1504A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461278 | ||||||
chr17:58461284
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1542+1498C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461284 | ||||||
chr17:58461469
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1542+1313G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461469 | ||||||
chr17:58461493
|
G | A | 1 | a0002c0002t0001g0258 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1542+1289C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461493 | ||||||
chr17:58461512
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1542+1270A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461512 | ||||||
chr17:58461647
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1542+1135C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461647 | ||||||
chr17:58461737
|
T | C | 2 | a0002c0002t0001g0189a0004c0011t0001g0230 | 2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1542+1045A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461737 | ||||||
chr17:58461743
|
G | A | 6 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01168.hp2 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542+1039C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461743 | ||||||
chr17:58461828
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1542+954G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461828 | ||||||
chr17:58461922
|
C | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1542+860G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58461922 | ||||||
chr17:58462127
|
C | A | 1 | a0001c0001t0001g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1542+655G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462127 | ||||||
chr17:58462127
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1542+655G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462127 | ||||||
chr17:58462131
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1542+651G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462131 | ||||||
chr17:58462431
|
T | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(18): Show | 23 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1542+351A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462431 | ||||||
chr17:58462469
|
A | C | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1542+313T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462469 | ||||||
chr17:58462529
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1542+253G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462529 | ||||||
chr17:58462636
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1542+146T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462636 | ||||||
chr17:58462749
|
G | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(65): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1542+33C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 4/5 | chr17 | 58462749 | ||||||
chr17:58463733
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1021-430G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58463733 | ||||||
chr17:58463753
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0074 | 2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1021-450C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58463753 | ||||||
chr17:58463891
|
A | T | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1021-588T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58463891 | ||||||
chr17:58464082
|
TA | T | 86 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1021-780delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464082 | ||||||
chr17:58464434
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1021-1131C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464434 | ||||||
chr17:58464486
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0166 | 2 | NA18998.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1021-1183G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464486 | ||||||
chr17:58464823
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1021-1520C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464823 | ||||||
chr17:58464823
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1021-1520C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464823 | ||||||
chr17:58464903
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1021-1600A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58464903 | ||||||
chr17:58465177
|
CTTTTCTT others(5): Show |
C | 10 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(7): Show | 11 | HG02055.hp1 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020+1696_1020+170 others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465177 | ||||||
chr17:58465182
|
C | CT | 53 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(50): Show | 55 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1020+1702dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465182 | ||||||
chr17:58465182
|
CT | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0037others(12): Show | 15 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1020+1702delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465182 | ||||||
chr17:58465252
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1020+1633G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465252 | ||||||
chr17:58465604
|
C | G | 2 | a0001c0005t0001g0069a0001c0005t0001g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1020+1281G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465604 | ||||||
chr17:58465615
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1020+1270C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465615 | ||||||
chr17:58465624
|
CA | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1020+1260delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465624 | ||||||
chr17:58465638
|
A | G | 1 | a0001c0001t0010g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1020+1247T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465638 | ||||||
chr17:58465824
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1020+1061C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465824 | ||||||
chr17:58465831
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1020+1054A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465831 | ||||||
chr17:58465956
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0213 | 2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1020+929G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465956 | ||||||
chr17:58465979
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1020+906T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58465979 | ||||||
chr17:58466063
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1020+822A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466063 | ||||||
chr17:58466076
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1020+809A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466076 | ||||||
chr17:58466189
|
C | T | 4 | a0002c0002t0001g0171a0002c0002t0001g0249a0002c0002t0001g0259others(1): Show | 4 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+696G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466189 | ||||||
chr17:58466359
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1020+526G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466359 | ||||||
chr17:58466370
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0106 | 3 | HG01168.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1020+515G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466370 | ||||||
chr17:58466465
|
T | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0085others(10): Show | 13 | HG00558.hp2 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1020+420A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466465 | ||||||
chr17:58466715
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1020+170A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466715 | ||||||
chr17:58466726
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1020+159T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466726 | ||||||
chr17:58466823
|
T | G | 1 | a0001c0001t0001g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1020+62A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 3/5 | chr17 | 58466823 | ||||||
chr17:58467013
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.926-34G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467013 | ||||||
chr17:58467069
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.926-90A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467069 | ||||||
chr17:58467424
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG02451.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.926-445G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467424 | ||||||
chr17:58467687
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.926-708A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467687 | ||||||
chr17:58467708
|
T | G | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.926-729A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467708 | ||||||
chr17:58467908
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-929G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467908 | ||||||
chr17:58467983
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.926-1004G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58467983 | ||||||
chr17:58468039
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0298 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.926-1060G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468039 | ||||||
chr17:58468094
|
G | T | 1 | a0002c0002t0001g0258 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.926-1115C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468094 | ||||||
chr17:58468116
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.926-1137T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468116 | ||||||
chr17:58468469
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-1490A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468469 | ||||||
chr17:58468556
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.926-1577T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468556 | ||||||
chr17:58468859
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.926-1880C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58468859 | ||||||
chr17:58469098
|
G | GA | 78 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0022others(75): Show | 80 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.926-2120dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469098 | ||||||
chr17:58469138
|
A | T | 2 | a0001c0005t0001g0069a0001c0005t0001g0073 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.926-2159T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469138 | ||||||
chr17:58469163
|
A | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.926-2184T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469163 | ||||||
chr17:58469364
|
T | A | 86 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.926-2385A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469364 | ||||||
chr17:58469842
|
T | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-2863A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469842 | ||||||
chr17:58469848
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.926-2869A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58469848 | ||||||
chr17:58470019
|
A | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-3040T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470019 | ||||||
chr17:58470024
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0209 | 2 | HG00099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.926-3045C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470024 | ||||||
chr17:58470042
|
C | A | 27 | a0002c0002t0001g0050a0002c0002t0001g0171a0002c0002t0001g0225others(24): Show | 27 | HG01261.hp1 HG01943.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.926-3063G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470042 | ||||||
chr17:58470176
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.926-3197G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470176 | ||||||
chr17:58470798
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.926-3819G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470798 | ||||||
chr17:58470920
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.926-3941G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58470920 | ||||||
chr17:58471059
|
T | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 129 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.926-4080A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471059 | ||||||
chr17:58471106
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.926-4127C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471106 | ||||||
chr17:58471397
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.926-4418C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471397 | ||||||
chr17:58471439
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-4460C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471439 | ||||||
chr17:58471450
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.926-4471T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471450 | ||||||
chr17:58471556
|
AT | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305others(1): Show | 4 | HG00642.hp1 HG03704.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-4578delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471556 | ||||||
chr17:58471621
|
C | CT | 293 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.926-4643dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471621 | ||||||
chr17:58471638
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.926-4659G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471638 | ||||||
chr17:58471787
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.926-4808C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471787 | ||||||
chr17:58471796
|
G | C | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.926-4817C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471796 | ||||||
chr17:58471844
|
G | C | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.926-4865C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471844 | ||||||
chr17:58471879
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-4900C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471879 | ||||||
chr17:58471901
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-4922C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471901 | ||||||
chr17:58471946
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.926-4967G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58471946 | ||||||
chr17:58472309
|
C | A | 2 | a0001c0001t0004g0196a0001c0001t0004g0212 | 2 | HG04184.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.926-5330G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472309 | ||||||
chr17:58472310
|
C | A | 86 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(83): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.926-5331G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472310 | ||||||
chr17:58472311
|
A | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(93): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.926-5332T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472311 | ||||||
chr17:58472647
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.926-5668A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472647 | ||||||
chr17:58472926
|
T | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-5947A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472926 | ||||||
chr17:58472939
|
C | T | 68 | a0001c0001t0001g0008a0001c0001t0001g0229a0001c0001t0001g0250others(65): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.926-5960G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58472939 | ||||||
chr17:58473052
|
G | C | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.926-6073C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473052 | ||||||
chr17:58473074
|
C | G | 1 | a0002c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.926-6095G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473074 | ||||||
chr17:58473165
|
A | C | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.926-6186T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473165 | ||||||
chr17:58473327
|
T | G | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-6348A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473327 | ||||||
chr17:58473443
|
T | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 129 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.925+6450A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473443 | ||||||
chr17:58473591
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.925+6302C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473591 | ||||||
chr17:58473778
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.925+6115T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473778 | ||||||
chr17:58473896
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.925+5997G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473896 | ||||||
chr17:58473931
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0266a0001c0001t0001g0267 | 4 | HG02622.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+5962T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473931 | ||||||
chr17:58473932
|
A | G | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+5961T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473932 | ||||||
chr17:58473954
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925+5939A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58473954 | ||||||
chr17:58474096
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+5797C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474096 | ||||||
chr17:58474389
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.925+5504G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474389 | ||||||
chr17:58474464
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.925+5429A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474464 | ||||||
chr17:58474473
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.925+5420A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474473 | ||||||
chr17:58474524
|
T | C | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.925+5369A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474524 | ||||||
chr17:58474691
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.925+5202C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474691 | ||||||
chr17:58474827
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0125a0001c0001t0001g0154 | 3 | HG01496.hp1 HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.925+5066G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474827 | ||||||
chr17:58474843
|
A | G | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.925+5050T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474843 | ||||||
chr17:58474992
|
A | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(94): Show | 98 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.925+4901T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58474992 | ||||||
chr17:58475042
|
C | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+4851G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475042 | ||||||
chr17:58475145
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.925+4748T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475145 | ||||||
chr17:58475541
|
A | G | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.925+4352T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475541 | ||||||
chr17:58475692
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.925+4201C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475692 | ||||||
chr17:58475899
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.925+3994T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58475899 | ||||||
chr17:58476227
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+3666G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476227 | ||||||
chr17:58476235
|
C | CTCTTCAT others(20): Show |
2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+3631_925+3657d others(29): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476235 | ||||||
chr17:58476324
|
T | G | 1 | a0003c0003t0008g0322 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.925+3569A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476324 | ||||||
chr17:58476347
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.925+3546C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476347 | ||||||
chr17:58476770
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.925+3123T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476770 | ||||||
chr17:58476868
|
G | GT | 6 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 6 | HG02602.hp1 HG02738.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+3024dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476868 | ||||||
chr17:58476996
|
A | G | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.925+2897T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58476996 | ||||||
chr17:58477115
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.925+2778T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477115 | ||||||
chr17:58477116
|
C | CT | 18 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(15): Show | 18 | HG00438.hp2 HG01261.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.925+2776dupA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477116 | ||||||
chr17:58477116
|
CT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(14): Show | 19 | HG00558.hp1 HG01243.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+2776delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477116 | ||||||
chr17:58477129
|
T | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(119): Show | 126 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.925+2764A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477129 | ||||||
chr17:58477129
|
T | TC | 3 | a0001c0001t0001g0085a0001c0001t0001g0094a0001c0001t0001g0132 | 3 | NA18949.hp2 NA18990.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.925+2763_925+2764i others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477129 | ||||||
chr17:58477150
|
T | C | 1 | a0002c0002t0001g0247 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.925+2743A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477150 | ||||||
chr17:58477173
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.925+2720C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477173 | ||||||
chr17:58477181
|
G | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.925+2712C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477181 | ||||||
chr17:58477341
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.925+2552G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477341 | ||||||
chr17:58477362
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0195 | 2 | HG00438.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.925+2531G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477362 | ||||||
chr17:58477374
|
C | T | 1 | a0001c0001t0010g0014 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.925+2519G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477374 | ||||||
chr17:58477426
|
T | A | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+2467A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477426 | ||||||
chr17:58477462
|
CT | C | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.925+2430delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477462 | ||||||
chr17:58477464
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0005g0012a0001c0001t0005g0013others(1): Show | 4 | HG00639.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+2429A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477464 | ||||||
chr17:58477520
|
C | T | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+2373G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477520 | ||||||
chr17:58477523
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.925+2370C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477523 | ||||||
chr17:58477545
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.925+2348G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477545 | ||||||
chr17:58477592
|
T | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0236 | 2 | NA18991.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.925+2301A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477592 | ||||||
chr17:58477627
|
T | G | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 129 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.925+2266A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477627 | ||||||
chr17:58477667
|
A | G | 1 | a0002c0002t0001g0248 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.925+2226T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477667 | ||||||
chr17:58477682
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 7 | HG01243.hp2 HG02572.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+2211C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477682 | ||||||
chr17:58477688
|
C | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 129 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.925+2205G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477688 | ||||||
chr17:58477693
|
C | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.925+2200G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477693 | ||||||
chr17:58477726
|
T | C | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.925+2167A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477726 | ||||||
chr17:58477986
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.925+1907A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58477986 | ||||||
chr17:58478171
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.925+1722G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478171 | ||||||
chr17:58478270
|
A | AAAAT | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0031others(78): Show | 83 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.925+1619_925+1622d others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478270 | ||||||
chr17:58478280
|
A | AAT | 4 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0060others(1): Show | 5 | HG01106.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+1611_925+1612d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478280 | ||||||
chr17:58478280
|
A | AATAAAT | 48 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0030others(45): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.925+1612_925+1613i others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478280 | ||||||
chr17:58478282
|
T | TAA | 163 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0035others(160): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.925+1610_925+1611i others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478282 | ||||||
chr17:58478284
|
T | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0102others(5): Show | 8 | HG01069.hp2 HG01070.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+1609A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478284 | ||||||
chr17:58478300
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0152 | 2 | HG04228.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925+1593A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478300 | ||||||
chr17:58478302
|
C | T | 106 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0055others(103): Show | 109 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.925+1591G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478302 | ||||||
chr17:58478353
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.925+1540A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478353 | ||||||
chr17:58478384
|
G | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(92): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.925+1509C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478384 | ||||||
chr17:58478475
|
C | CA | 7 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0108others(4): Show | 7 | HG00621.hp2 HG01081.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+1417dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478475 | ||||||
chr17:58478486
|
AAAAAG | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0051others(10): Show | 14 | HG02055.hp1 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.925+1402_925+1406d others(7): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478486 | ||||||
chr17:58478486
|
AAAAAGAA others(3): Show |
A | 4 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0175others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+1397_925+1406d others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478486 | ||||||
chr17:58478539
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0208 | 2 | NA19011.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.925+1354A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478539 | ||||||
chr17:58478864
|
CA | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(171): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.925+1028delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478864 | ||||||
chr17:58478960
|
G | A | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+933C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58478960 | ||||||
chr17:58479129
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.925+764T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479129 | ||||||
chr17:58479287
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.925+606C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479287 | ||||||
chr17:58479508
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.925+385C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479508 | ||||||
chr17:58479601
|
C | T | 3 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0010g0014 | 3 | HG02257.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.925+292G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 2/5 | chr17 | 58479601 | ||||||
chr17:58480400
|
AAAC | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(291): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.551-136_551-134del others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480400 | ||||||
chr17:58480476
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.551-209C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480476 | ||||||
chr17:58480700
|
C | A | 1 | a0001c0001t0001g0301 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.551-433G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480700 | ||||||
chr17:58480762
|
G | GCTAT | 115 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0021others(112): Show | 117 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.551-499_551-496dup others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | ||||||
chr17:58480762
|
G | GCTATCTA others(1): Show |
84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0015others(81): Show | 87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.551-503_551-496dup others(8): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | ||||||
chr17:58480762
|
G | GCTATCTA others(5): Show |
54 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0030others(51): Show | 55 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.551-507_551-496dup others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | ||||||
chr17:58480762
|
G | GCTATCTA others(9): Show |
13 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0121others(10): Show | 13 | HG01358.hp1 HG02148.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.551-511_551-496dup others(16): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | ||||||
chr17:58480762
|
GCTATCTA others(5): Show |
G | 3 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-507_551-496del others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480762 | ||||||
chr17:58480880
|
C | T | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.551-613G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58480880 | ||||||
chr17:58481155
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.551-888A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481155 | ||||||
chr17:58481238
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.551-971G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481238 | ||||||
chr17:58481334
|
T | C | 1 | a0004c0011t0001g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.551-1067A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481334 | ||||||
chr17:58481557
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(293): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.551-1290C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481557 | ||||||
chr17:58481644
|
T | C | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.551-1377A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481644 | ||||||
chr17:58481814
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.551-1547T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58481814 | ||||||
chr17:58482120
|
T | TAAAC | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.551-1854_551-1853i others(6): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482120 | ||||||
chr17:58482526
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0305 | 3 | HG00642.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.551-2259A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482526 | ||||||
chr17:58482709
|
C | CA | 59 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0028others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.551-2443dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | ||||||
chr17:58482709
|
C | CAA | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 86 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.551-2444_551-2443d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | ||||||
chr17:58482709
|
C | CAAA | 16 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0071others(13): Show | 16 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.551-2445_551-2443d others(5): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | ||||||
chr17:58482709
|
CA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0055others(7): Show | 11 | HG01515.hp1 HG01515.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.551-2443delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | ||||||
chr17:58482709
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.551-2452_551-2443d others(12): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | ||||||
chr17:58482709
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA18979.hp1 NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.551-2458_551-2443d others(18): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482709 | ||||||
chr17:58482837
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.551-2570C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482837 | ||||||
chr17:58482940
|
T | TA | 4 | a0001c0001t0001g0295a0002c0002t0001g0050a0002c0002t0001g0279others(1): Show | 4 | HG02055.hp1 HG04115.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-2674_551-2673i others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482940 | ||||||
chr17:58482941
|
T | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0074a0001c0001t0001g0229others(65): Show | 70 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.551-2674A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482941 | ||||||
chr17:58482941
|
TA | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0060others(19): Show | 23 | HG01069.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.551-2675delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482941 | ||||||
chr17:58482997
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.551-2730C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58482997 | ||||||
chr17:58483015
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | NA18979.hp1 NA18984.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.551-2748T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483015 | ||||||
chr17:58483116
|
A | AT | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.551-2850_551-2849i others(3): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483116 | ||||||
chr17:58483480
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-3213T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483480 | ||||||
chr17:58483499
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0055others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-3232A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58483499 | ||||||
chr17:58484117
|
A | T | 1 | a0002c0002t0001g0292 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.550+3608T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484117 | ||||||
chr17:58484205
|
G | GA | 12 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0108others(9): Show | 12 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.550+3519dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484205 | ||||||
chr17:58484581
|
C | T | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.550+3144G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484581 | ||||||
chr17:58484591
|
GA | G | 87 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(84): Show | 87 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.550+3133delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484591 | ||||||
chr17:58484701
|
G | A | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.550+3024C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484701 | ||||||
chr17:58484771
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(95): Show | 99 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.550+2954G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484771 | ||||||
chr17:58484924
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.550+2801T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484924 | ||||||
chr17:58484945
|
AT | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0022others(48): Show | 52 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.550+2779delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484945 | ||||||
chr17:58484945
|
ATT | A | 113 | a0001c0001t0001g0003a0001c0001t0001g0039a0001c0001t0001g0040others(110): Show | 115 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.550+2778_550+2779d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484945 | ||||||
chr17:58484945
|
ATTT | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 148 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.550+2777_550+2779d others(5): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58484945 | ||||||
chr17:58485103
|
C | T | 1 | a0002c0002t0001g0171 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.550+2622G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485103 | ||||||
chr17:58485174
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0302a0001c0001t0001g0303 | 3 | HG00558.hp2 NA18747.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.550+2551G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485174 | ||||||
chr17:58485312
|
T | C | 6 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+2413A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485312 | ||||||
chr17:58485348
|
T | A | 2 | a0002c0002t0001g0284a0002c0002t0001g0285 | 2 | NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.550+2377A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485348 | ||||||
chr17:58485435
|
G | A | 2 | a0001c0004t0001g0169a0001c0004t0001g0319 | 2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.550+2290C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485435 | ||||||
chr17:58485619
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.550+2106G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485619 | ||||||
chr17:58485690
|
T | G | 2 | a0002c0002t0001g0296a0002c0002t0001g0297 | 2 | NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.550+2035A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485690 | ||||||
chr17:58485728
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.550+1997G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485728 | ||||||
chr17:58485746
|
C | CA | 149 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0037others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.550+1978dupT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485746 | ||||||
chr17:58485746
|
C | CAA | 15 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(12): Show | 15 | HG00438.hp1 HG02055.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.550+1977_550+1978d others(4): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485746 | ||||||
chr17:58485746
|
CA | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0301others(3): Show | 7 | HG00323.hp1 HG01099.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+1978delT | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485746 | ||||||
chr17:58485859
|
G | A | 295 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.550+1866C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485859 | ||||||
chr17:58485955
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0008g0322 | 3 | HG01257.hp1 HG01258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.550+1770C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58485955 | ||||||
chr17:58486089
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.550+1636G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486089 | ||||||
chr17:58486130
|
A | C | 1 | a0006c0008t0001g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.550+1595T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486130 | ||||||
chr17:58486191
|
T | C | 300 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.550+1534A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486191 | ||||||
chr17:58486314
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02486.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.550+1411C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486314 | ||||||
chr17:58486322
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 7 | HG01243.hp2 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+1403C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486322 | ||||||
chr17:58486327
|
T | A | 1 | a0001c0001t0001g0299 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.550+1398A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486327 | ||||||
chr17:58486412
|
G | T | 1 | a0002c0002t0001g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.550+1313C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486412 | ||||||
chr17:58486725
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0061 | 4 | HG02486.hp1 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+1000A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486725 | ||||||
chr17:58486887
|
T | C | 1 | a0002c0002t0001g0300 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.550+838A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486887 | ||||||
chr17:58486902
|
CT | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.550+822delA | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486902 | ||||||
chr17:58486902
|
CTT | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0301a0001c0001t0001g0302others(16): Show | 20 | HG00323.hp2 HG00558.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.550+821_550+822del others(2): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58486902 | ||||||
chr17:58487196
|
A | G | 3 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0010g0014 | 3 | HG02257.hp2 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+529T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487196 | ||||||
chr17:58487303
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+422A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487303 | ||||||
chr17:58487305
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+420A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487305 | ||||||
chr17:58487306
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+419C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487306 | ||||||
chr17:58487310
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+415G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487310 | ||||||
chr17:58487313
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+412G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487313 | ||||||
chr17:58487319
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+406G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487319 | ||||||
chr17:58487324
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+401C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487324 | ||||||
chr17:58487326
|
T | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+399A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487326 | ||||||
chr17:58487327
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+398A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487327 | ||||||
chr17:58487331
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+394G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487331 | ||||||
chr17:58487332
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+393C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487332 | ||||||
chr17:58487338
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+387G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487338 | ||||||
chr17:58487339
|
T | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+386A>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487339 | ||||||
chr17:58487341
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+384G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487341 | ||||||
chr17:58487343
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+382C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487343 | ||||||
chr17:58487345
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+380C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487345 | ||||||
chr17:58487347
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+378G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487347 | ||||||
chr17:58487348
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+377G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487348 | ||||||
chr17:58487351
|
A | C | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+374T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487351 | ||||||
chr17:58487353
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+372C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487353 | ||||||
chr17:58487355
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+370A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487355 | ||||||
chr17:58487356
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+369A>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487356 | ||||||
chr17:58487360
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+365C>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487360 | ||||||
chr17:58487362
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+363C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487362 | ||||||
chr17:58487364
|
A | C | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+361T>G | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487364 | ||||||
chr17:58487365
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+360G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487365 | ||||||
chr17:58487367
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+358C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487367 | ||||||
chr17:58487369
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+356C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487369 | ||||||
chr17:58487374
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+351A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487374 | ||||||
chr17:58487375
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+350G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487375 | ||||||
chr17:58487378
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+347T>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487378 | ||||||
chr17:58487379
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+346C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487379 | ||||||
chr17:58487380
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+345C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487380 | ||||||
chr17:58487383
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+342C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487383 | ||||||
chr17:58487384
|
G | GAATTATC others(8): Show |
1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+340_550+341ins others(15): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487384 | ||||||
chr17:58487387
|
A | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+338T>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487387 | ||||||
chr17:58487389
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+336G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487389 | ||||||
chr17:58487391
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+334C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487391 | ||||||
chr17:58487397
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+328A>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487397 | ||||||
chr17:58487399
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+326G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487399 | ||||||
chr17:58487402
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+323G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487402 | ||||||
chr17:58487403
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+322G>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487403 | ||||||
chr17:58487405
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+320C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487405 | ||||||
chr17:58487406
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+319C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487406 | ||||||
chr17:58487417
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+308C>A | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487417 | ||||||
chr17:58487418
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+307C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487418 | ||||||
chr17:58487419
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+306C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487419 | ||||||
chr17:58487422
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+303G>C | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487422 | ||||||
chr17:58487429
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+296C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487429 | ||||||
chr17:58487430
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+295C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487430 | ||||||
chr17:58487433
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.550+292G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487433 | ||||||
chr17:58487434
|
G | A | 2 | a0001c0001t0001g0320a0001c0004t0001g0319 | 2 | HG01346.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.550+291C>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487434 | ||||||
chr17:58487611
|
C | A | 1 | a0002c0002t0001g0321 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.550+114G>T | HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 1/5 | chr17 | 58487611 |