geneid | 3298 |
---|---|
ensemblid | ENSG00000025156.13 |
hgncid | 5225 |
symbol | HSF2 |
name | heat shock transcription factor 2 |
refseq_nuc | NM_004506.4 |
refseq_prot | NP_004497.1 |
ensembl_nuc | ENST00000368455.9 |
ensembl_prot | ENSP00000357440.4 |
mane_status | MANE Select |
chr | chr6 |
start | 122399652 |
end | 122433119 |
strand | + |
ver | v1.2 |
region | chr6:122399652-122433119 |
region5000 | chr6:122394652-122438119 |
regionname0 | HSF2_chr6_122399652_122433119 |
regionname5000 | HSF2_chr6_122394652_122438119 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 536 | 386 | 86 | 70 | 184 | 14 | 30 | 138 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1611 | 366 | 86 | 68 | 167 | 13 | 30 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
c0002 | 0/0 | 1611 | 13 | 0 | 0 | 13 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
c0003 | 0/0 | 1611 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
c0004 | 0/0 | 1611 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
c0005 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 986 | 181 | 37 | 40 | 79 | 6 | 19 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0002 | 1/0 | 986 | 139 | 30 | 19 | 78 | 4 | 7 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0003 | 0/1 | 998 | 55 | 11 | 10 | 26 | 3 | 4 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0004 | 0/0 | 986 | 5 | 5 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0005 | 0/0 | 986 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0006 | 0/0 | 986 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0007 | 0/0 | 986 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
t0008 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 21 | 0 | 1 | 18 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0002 | 0/0 | 20 | 0 | 4 | 12 | 2 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0003 | 0/0 | 16 | 0 | 2 | 12 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0004 | 0/0 | 13 | 2 | 1 | 10 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0005 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0006 | 0/0 | 9 | 0 | 8 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0008 | 0/0 | 7 | 2 | 4 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0009 | 0/0 | 7 | 1 | 4 | 0 | 1 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0013 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0027 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1611 | 366 | 86 | 68 | 167 | 13 | 30 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0002 | 0/0 | 1611 | 13 | 0 | 0 | 13 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0003 | 0/0 | 1611 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0004 | 0/0 | 1611 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0005 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2596 | 180 | 37 | 40 | 79 | 5 | 19 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0002 | 1/0 | 2596 | 122 | 30 | 19 | 61 | 4 | 7 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0003 | 0/1 | 2608 | 53 | 11 | 8 | 26 | 3 | 4 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0004 | 0/0 | 2596 | 5 | 5 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0005 | 0/0 | 2596 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0006 | 0/0 | 2596 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0007 | 0/0 | 2596 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0001t0008 | 0/0 | 2596 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0002t0002 | 0/0 | 2596 | 13 | 0 | 0 | 13 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0003t0002 | 0/0 | 2596 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0004t0003 | 0/0 | 2608 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
a0001c0005t0001 | 0/0 | 2596 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | copy fasta | chr6 | 122394652 | 122438119 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 0 | 0 | 18 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0006 | 0/0 | 9 | 0 | 8 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0008 | 0/0 | 7 | 2 | 4 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0009 | 0/0 | 7 | 1 | 4 | 0 | 1 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0003 | 0/0 | 16 | 0 | 2 | 12 | 0 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0004 | 0/0 | 12 | 2 | 1 | 9 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0013 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0027 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0002 | 0/0 | 17 | 0 | 2 | 11 | 2 | 2 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0001t0008g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0004t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
a0001c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0199 | EUR | GBR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00099 | hp2 | a0001 | c0005 | t0001 | g0168 | EUR | GBR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | FIN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00544 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01168 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01169 | hp1 | a0001 | c0004 | t0003 | g0002 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0107 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0214 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18964 | hp1 | a0001 | c0003 | t0002 | g0215 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18990 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19010 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0201 | REF | REF | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0027 | REF | REF | HSF2_chr6_122394652_122438119 | HSF2 | chr6 | 122394652 | 122438119 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:122412393
|
C | T | 1 | a0001c0004 | 2 | HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.114C>T | p.Val38Val | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 2/13 | 200/2596 | 114/1611 | 38/536 | chr6 | 122412393 | ||
chr6:122422874
|
A | T | 2 | a0001c0002a0001c0003 | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
synonymous_variant | LOW | c.987A>T | p.Leu329Leu | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/13 | 1073/2596 | 987/1611 | 329/536 | chr6 | 122422874 | ||
chr6:122423632
|
C | T | 1 | a0001c0005 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1122C>T | p.Phe374Phe | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/13 | 1208/2596 | 1122/1611 | 374/536 | chr6 | 122423632 | ||
chr6:122431468
|
A | C | 1 | a0001c0003 | 4 | HG00544.hp1 NA18612.hp2 NA18964.hp1 others(1): Show |
synonymous_variant | LOW | c.1269A>C | p.Val423Val | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/13 | 1355/2596 | 1269/1611 | 423/536 | chr6 | 122431468 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:122399661
|
G | A | 5 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(2): Show | 186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | 77 | chr6 | 122399661 | |||||
chr6:122399668
|
T | TGCCGTAG others(5): Show |
2 | a0001c0001t0003a0001c0004t0003 | 55 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-65_-54dupTAGCTGCC others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | 53 | INFO_REALIGN_3_PRIME | chr6 | 122399668 | ||||
chr6:122399671
|
C | T | 1 | a0001c0001t0008 | 1 | NA19010.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-67C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | chr6 | 122399671 | ||||||
chr6:122399704
|
G | T | 1 | a0001c0001t0007 | 1 | HG01515.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | chr6 | 122399704 | ||||||
chr6:122399728
|
C | T | 1 | a0001c0001t0006 | 1 | HG01975.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/13 | chr6 | 122399728 | ||||||
chr6:122432223
|
C | T | 1 | a0001c0001t0005 | 3 | HG02109.hp1 HG02559.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 13/13 | 3 | chr6 | 122432223 | |||||
chr6:122432515
|
C | T | 1 | a0001c0001t0004 | 5 | HG02818.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*295C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 13/13 | 295 | chr6 | 122432515 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:122399875
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.93+45C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122399875 | ||||||
chr6:122399922
|
C | G | 1 | a0001c0001t0002g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.93+92C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122399922 | ||||||
chr6:122400064
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.93+234C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400064 | ||||||
chr6:122400167
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.93+337T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400167 | ||||||
chr6:122400276
|
G | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+446G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400276 | ||||||
chr6:122400305
|
A | G | 46 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(43): Show | 75 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.93+475A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400305 | ||||||
chr6:122400365
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.93+535A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400365 | ||||||
chr6:122400687
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 5 | HG01081.hp1 HG01109.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.93+857A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400687 | ||||||
chr6:122400747
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.93+917C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400747 | ||||||
chr6:122400829
|
G | A | 29 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(26): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+999G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122400829 | ||||||
chr6:122401163
|
G | C | 46 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(43): Show | 75 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.93+1333G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401163 | ||||||
chr6:122401374
|
C | G | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.93+1544C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401374 | ||||||
chr6:122401456
|
T | C | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+1626T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401456 | ||||||
chr6:122401585
|
A | AT | 9 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(6): Show | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.93+1756dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122401585 | |||||
chr6:122401663
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0176others(4): Show | 12 | HG01255.hp1 HG02004.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.93+1833A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401663 | ||||||
chr6:122401683
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100 | 3 | HG02615.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.93+1853G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401683 | ||||||
chr6:122401772
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.93+1942A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122401772 | ||||||
chr6:122402151
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93+2321C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402151 | ||||||
chr6:122402314
|
T | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 8 | NA18942.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+2484T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402314 | ||||||
chr6:122402562
|
G | GT | 6 | a0001c0001t0001g0038a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 8 | HG00609.hp1 HG01884.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+2744dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122402562 | |||||
chr6:122402677
|
C | A | 29 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(26): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+2847C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402677 | ||||||
chr6:122402677
|
C | G | 1 | a0001c0001t0001g0037 | 2 | NA18990.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.93+2847C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402677 | ||||||
chr6:122402715
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93+2885G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402715 | ||||||
chr6:122402844
|
C | T | 3 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0209 | 3 | HG02083.hp2 NA18945.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.93+3014C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122402844 | ||||||
chr6:122403329
|
G | A | 2 | a0001c0001t0003g0183a0001c0001t0003g0184 | 2 | HG02080.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.93+3499G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403329 | ||||||
chr6:122403379
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.93+3549G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403379 | ||||||
chr6:122403454
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.93+3624G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403454 | ||||||
chr6:122403518
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG03491.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.93+3688G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403518 | ||||||
chr6:122403754
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.93+3924G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403754 | ||||||
chr6:122403868
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.93+4038T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403868 | ||||||
chr6:122403918
|
T | C | 1 | a0001c0001t0004g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.93+4088T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403918 | ||||||
chr6:122403959
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.93+4129A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122403959 | ||||||
chr6:122404264
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.93+4434C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404264 | ||||||
chr6:122404591
|
T | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.93+4761T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404591 | ||||||
chr6:122404598
|
A | AGG | 46 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(43): Show | 75 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.93+4768_93+4769ins others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404598 | ||||||
chr6:122404726
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.93+4896C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404726 | ||||||
chr6:122404782
|
G | A | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.93+4952G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404782 | ||||||
chr6:122404863
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.93+5033A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122404863 | ||||||
chr6:122405162
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.93+5332G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405162 | ||||||
chr6:122405250
|
G | A | 6 | a0001c0001t0002g0018a0001c0001t0002g0076a0001c0001t0002g0077others(3): Show | 8 | NA18956.hp2 NA18960.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+5420G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405250 | ||||||
chr6:122405252
|
C | G | 1 | a0001c0001t0002g0028 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.93+5422C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405252 | ||||||
chr6:122405256
|
T | TA | 9 | a0001c0001t0001g0030a0001c0001t0001g0105a0001c0001t0001g0106others(6): Show | 10 | HG01433.hp1 HG01515.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+5445dupA | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122405256 | |||||
chr6:122405256
|
TA | T | 18 | a0001c0001t0001g0044a0001c0001t0001g0162a0001c0001t0001g0163others(15): Show | 19 | HG00099.hp2 HG01257.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+5445delA | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122405256 | |||||
chr6:122405369
|
A | G | 29 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(26): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.93+5539A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405369 | ||||||
chr6:122405408
|
G | C | 1 | a0001c0002t0002g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.93+5578G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405408 | ||||||
chr6:122405443
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 8 | NA18942.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+5613A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405443 | ||||||
chr6:122405894
|
T | C | 2 | a0001c0001t0003g0217a0001c0001t0003g0218 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.93+6064T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122405894 | ||||||
chr6:122406310
|
A | G | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-6063A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406310 | ||||||
chr6:122406521
|
G | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.94-5852G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406521 | ||||||
chr6:122406602
|
G | A | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-5771G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406602 | ||||||
chr6:122406682
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.94-5691G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406682 | ||||||
chr6:122406775
|
AG | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.94-5597delG | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406775 | ||||||
chr6:122406819
|
G | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-5554G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406819 | ||||||
chr6:122406959
|
G | C | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0162 | 3 | HG00597.hp2 HG02132.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.94-5414G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406959 | ||||||
chr6:122406996
|
A | G | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.94-5377A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122406996 | ||||||
chr6:122407049
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-5324A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407049 | ||||||
chr6:122407125
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94-5248G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407125 | ||||||
chr6:122407426
|
A | G | 1 | a0001c0001t0003g0211 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.94-4947A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407426 | ||||||
chr6:122407591
|
GT | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.94-4771delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407591 | |||||
chr6:122407602
|
T | A | 9 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(6): Show | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.94-4771T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407602 | ||||||
chr6:122407719
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0160 | 3 | HG02027.hp1 NA18948.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.94-4654C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407719 | ||||||
chr6:122407727
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(31): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.94-4646A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407727 | ||||||
chr6:122407734
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.94-4639A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407734 | ||||||
chr6:122407765
|
C | T | 27 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(24): Show | 47 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.94-4608C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407765 | ||||||
chr6:122407838
|
G | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.94-4535G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407838 | ||||||
chr6:122407885
|
G | C | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.94-4488G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122407885 | ||||||
chr6:122407961
|
C | CAG | 35 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(32): Show | 65 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.94-4387_94-4386dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | |||||
chr6:122407961
|
C | CAGAG | 3 | a0001c0001t0002g0024a0001c0001t0002g0052a0001c0001t0002g0096 | 4 | HG02486.hp2 HG04199.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-4389_94-4386dup others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | |||||
chr6:122407961
|
CAG | C | 2 | a0001c0001t0001g0160a0001c0001t0002g0025 | 3 | HG01257.hp1 HG01258.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.94-4387_94-4386del others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | |||||
chr6:122407961
|
CAGAG | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.94-4389_94-4386del others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122407961 | |||||
chr6:122408021
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.94-4352C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408021 | ||||||
chr6:122408083
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.94-4290T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408083 | ||||||
chr6:122408087
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.94-4286A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408087 | ||||||
chr6:122408105
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.94-4268T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408105 | ||||||
chr6:122408192
|
C | T | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-4181C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408192 | ||||||
chr6:122408335
|
T | TA | 31 | a0001c0001t0001g0060a0001c0001t0001g0102a0001c0001t0002g0003others(28): Show | 55 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.94-4025dupA | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122408335 | |||||
chr6:122408386
|
A | T | 5 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3987A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408386 | ||||||
chr6:122408482
|
G | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG02027.hp2 NA19002.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.94-3891G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408482 | ||||||
chr6:122408503
|
T | A | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-3870T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408503 | ||||||
chr6:122408522
|
A | C | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(2): Show | 5 | NA18956.hp2 NA18960.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-3851A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408522 | ||||||
chr6:122408616
|
A | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.94-3757A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408616 | ||||||
chr6:122408625
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-3748C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408625 | ||||||
chr6:122408747
|
A | G | 6 | a0001c0001t0002g0052a0001c0001t0002g0064a0001c0001t0002g0065others(3): Show | 6 | HG01261.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-3626A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408747 | ||||||
chr6:122408768
|
C | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-3605C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408768 | ||||||
chr6:122408848
|
A | AT | 63 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 95 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.94-3509dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122408848 | |||||
chr6:122408877
|
T | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.94-3496T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122408877 | ||||||
chr6:122409206
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.94-3167A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409206 | ||||||
chr6:122409280
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.94-3093G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409280 | ||||||
chr6:122409497
|
T | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.94-2876T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409497 | ||||||
chr6:122409544
|
A | G | 1 | a0001c0001t0003g0205 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.94-2829A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409544 | ||||||
chr6:122409545
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.94-2828C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409545 | ||||||
chr6:122409657
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.94-2716A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409657 | ||||||
chr6:122409759
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0144a0001c0001t0003g0218 | 8 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-2614A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409759 | ||||||
chr6:122409813
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0108others(4): Show | 14 | HG00323.hp1 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.94-2560T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409813 | ||||||
chr6:122409873
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94-2500C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122409873 | ||||||
chr6:122410261
|
T | A | 29 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(26): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.94-2112T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410261 | ||||||
chr6:122410498
|
C | T | 2 | a0001c0001t0003g0203a0001c0001t0003g0204 | 2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.94-1875C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410498 | ||||||
chr6:122410550
|
C | G | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94-1823C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410550 | ||||||
chr6:122410673
|
C | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 190 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.94-1700C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410673 | ||||||
chr6:122410815
|
T | G | 2 | a0001c0001t0003g0192a0001c0001t0003g0193 | 2 | NA18953.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.94-1558T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410815 | ||||||
chr6:122410945
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.94-1428T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410945 | ||||||
chr6:122410948
|
G | GT | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.94-1409dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122410948 | |||||
chr6:122410948
|
G | GTT | 9 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(6): Show | 9 | HG00621.hp2 HG00741.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.94-1410_94-1409dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122410948 | |||||
chr6:122410948
|
G | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18942.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.94-1425G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122410948 | ||||||
chr6:122410948
|
GT | G | 36 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(33): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.94-1409delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 122410948 | |||||
chr6:122411011
|
T | G | 1 | a0001c0001t0003g0194 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.94-1362T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411011 | ||||||
chr6:122411041
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0007g0107 | 2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.94-1332C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411041 | ||||||
chr6:122411095
|
T | A | 30 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(27): Show | 54 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.94-1278T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411095 | ||||||
chr6:122411239
|
A | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.94-1134A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411239 | ||||||
chr6:122411307
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94-1066G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411307 | ||||||
chr6:122411323
|
G | C | 1 | a0001c0001t0003g0195 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.94-1050G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411323 | ||||||
chr6:122411327
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.94-1046T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411327 | ||||||
chr6:122411347
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0116 | 3 | HG03704.hp1 HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.94-1026T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411347 | ||||||
chr6:122411612
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.94-761T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411612 | ||||||
chr6:122411641
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.94-732T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411641 | ||||||
chr6:122411643
|
T | G | 1 | a0001c0001t0002g0076 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.94-730T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411643 | ||||||
chr6:122411914
|
A | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.94-459A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122411914 | ||||||
chr6:122412025
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.94-348A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122412025 | ||||||
chr6:122412127
|
T | A | 1 | a0001c0001t0002g0053 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.94-246T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122412127 | ||||||
chr6:122412362
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.94-11T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 1/12 | chr6 | 122412362 | ||||||
chr6:122412781
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.330+17G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412781 | ||||||
chr6:122412822
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0117 | 3 | HG00735.hp1 HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.330+58G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412822 | ||||||
chr6:122412833
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.330+69C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412833 | ||||||
chr6:122412909
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.330+145C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412909 | ||||||
chr6:122412924
|
A | G | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.330+160A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412924 | ||||||
chr6:122412930
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.330+166G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122412930 | ||||||
chr6:122413090
|
AT | A | 33 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(30): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.330+332delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 122413090 | |||||
chr6:122413177
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0001g0154 | 2 | HG02165.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.331-348A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122413177 | ||||||
chr6:122413303
|
C | A | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.331-222C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122413303 | ||||||
chr6:122413323
|
A | AT | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.331-194dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr6 | 122413323 | |||||
chr6:122413400
|
C | T | 29 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(26): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.331-125C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 3/12 | chr6 | 122413400 | ||||||
chr6:122413775
|
A | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0137 | 3 | HG02896.hp2 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.455+126A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413775 | ||||||
chr6:122413827
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 187 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.455+178G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413827 | ||||||
chr6:122413975
|
A | G | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.455+326A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413975 | ||||||
chr6:122413976
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.455+327T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122413976 | ||||||
chr6:122414035
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.455+386G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414035 | ||||||
chr6:122414038
|
T | G | 28 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(25): Show | 48 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.455+389T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414038 | ||||||
chr6:122414168
|
C | T | 4 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(1): Show | 4 | HG02615.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+519C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414168 | ||||||
chr6:122414473
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0030others(21): Show | 39 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.455+824C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414473 | ||||||
chr6:122414545
|
G | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.455+896G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414545 | ||||||
chr6:122414800
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.455+1151A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414800 | ||||||
chr6:122414819
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.455+1170G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122414819 | ||||||
chr6:122415097
|
A | T | 1 | a0001c0001t0002g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.456-1124A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415097 | ||||||
chr6:122415248
|
A | C | 1 | a0001c0001t0003g0208 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.456-973A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415248 | ||||||
chr6:122415281
|
T | C | 34 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(31): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.456-940T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415281 | ||||||
chr6:122415329
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.456-892A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415329 | ||||||
chr6:122415691
|
C | G | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.456-530C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415691 | ||||||
chr6:122415761
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.456-460C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415761 | ||||||
chr6:122415779
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.456-442C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415779 | ||||||
chr6:122415865
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.456-356A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415865 | ||||||
chr6:122415959
|
A | G | 33 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(30): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.456-262A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122415959 | ||||||
chr6:122416022
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.456-199T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416022 | ||||||
chr6:122416058
|
T | A | 1 | a0001c0001t0002g0054 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.456-163T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416058 | ||||||
chr6:122416110
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.456-111T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416110 | ||||||
chr6:122416171
|
T | G | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-50T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | chr6 | 122416171 | ||||||
chr6:122416181
|
AT | A | 13 | a0001c0001t0003g0196a0001c0001t0003g0199a0001c0001t0003g0200others(10): Show | 21 | HG00099.hp1 HG00544.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.456-30delT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 122416181 | |||||
chr6:122416314
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.531+18C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416314 | ||||||
chr6:122416490
|
A | G | 1 | a0001c0001t0001g0020 | 3 | NA18974.hp1 NA19083.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.531+194A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416490 | ||||||
chr6:122416514
|
G | T | 27 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(24): Show | 47 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.531+218G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416514 | ||||||
chr6:122416604
|
A | G | 5 | a0001c0001t0002g0014a0001c0001t0002g0081a0001c0001t0004g0014others(2): Show | 7 | HG02451.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+308A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416604 | ||||||
chr6:122416786
|
G | C | 1 | a0001c0001t0003g0217 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.531+490G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122416786 | ||||||
chr6:122417124
|
G | A | 34 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(31): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.531+828G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417124 | ||||||
chr6:122417770
|
A | G | 4 | a0001c0001t0003g0186a0001c0001t0003g0187a0001c0001t0003g0188others(1): Show | 4 | HG02615.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-1398A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417770 | ||||||
chr6:122417914
|
G | A | 1 | a0001c0001t0003g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.532-1254G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417914 | ||||||
chr6:122417917
|
T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.532-1251T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417917 | ||||||
chr6:122417930
|
T | G | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.532-1238T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417930 | ||||||
chr6:122417964
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.532-1204A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417964 | ||||||
chr6:122417999
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.532-1169T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122417999 | ||||||
chr6:122418005
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.532-1163A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418005 | ||||||
chr6:122418019
|
T | G | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.532-1149T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418019 | ||||||
chr6:122418032
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.532-1136T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418032 | ||||||
chr6:122418142
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.532-1026G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418142 | ||||||
chr6:122418178
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.532-990C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418178 | ||||||
chr6:122418198
|
C | T | 9 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(6): Show | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.532-970C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418198 | ||||||
chr6:122418400
|
A | G | 1 | a0001c0002t0002g0042 | 2 | NA18940.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.532-768A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418400 | ||||||
chr6:122418477
|
G | A | 10 | a0001c0001t0003g0217a0001c0002t0002g0010a0001c0002t0002g0023others(7): Show | 18 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.532-691G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418477 | ||||||
chr6:122418533
|
A | C | 1 | a0001c0001t0004g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.532-635A>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418533 | ||||||
chr6:122418670
|
C | T | 33 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(30): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.532-498C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418670 | ||||||
chr6:122418699
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.532-469T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418699 | ||||||
chr6:122418711
|
A | G | 4 | a0001c0001t0003g0198a0001c0001t0003g0202a0001c0001t0003g0203others(1): Show | 4 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-457A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418711 | ||||||
chr6:122418790
|
C | T | 9 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(6): Show | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.532-378C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 5/12 | chr6 | 122418790 | ||||||
chr6:122419280
|
T | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.593+51T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419280 | ||||||
chr6:122419295
|
T | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.593+66T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419295 | ||||||
chr6:122419329
|
G | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.593+100G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419329 | ||||||
chr6:122419387
|
T | G | 1 | a0001c0001t0001g0123 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.593+158T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419387 | ||||||
chr6:122419447
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.593+218C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419447 | ||||||
chr6:122419501
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.593+272A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419501 | ||||||
chr6:122419557
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.593+328T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419557 | ||||||
chr6:122419645
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.593+416T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 6/12 | chr6 | 122419645 | ||||||
chr6:122420227
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18986.hp1 | splice_region_variant&intron_variant | LOW | c.681+5T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420227 | ||||||
chr6:122420233
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.681+11A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420233 | ||||||
chr6:122420368
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.681+146A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420368 | ||||||
chr6:122420637
|
C | CTT | 35 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(32): Show | 57 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.681+422_681+423dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420637 | |||||
chr6:122420637
|
C | CTTT | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.681+421_681+423dup others(3): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420637 | |||||
chr6:122420700
|
C | CT | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.681+507dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420700
|
C | CTT | 23 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0060others(20): Show | 25 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.681+506_681+507dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420700
|
C | CTTT | 10 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0150others(7): Show | 12 | HG00099.hp1 HG02040.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+505_681+507dup others(3): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420700
|
C | CTTTT | 19 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0183others(16): Show | 36 | HG00544.hp2 HG00609.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.681+504_681+507dup others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420700
|
C | CTTTTT | 7 | a0001c0001t0003g0041a0001c0001t0003g0190a0001c0001t0003g0191others(4): Show | 8 | HG00423.hp2 HG00642.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+503_681+507dup others(5): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420700
|
CTTTTTTT | C | 9 | a0001c0001t0003g0217a0001c0002t0002g0010a0001c0002t0002g0023others(6): Show | 17 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+501_681+507del others(7): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420700
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.681+498_681+507del others(10): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122420700 | |||||
chr6:122420713
|
T | C | 8 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(5): Show | 16 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.681+491T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420713 | ||||||
chr6:122420714
|
T | C | 1 | a0001c0002t0002g0213 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.681+492T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420714 | ||||||
chr6:122420738
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.681+516A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420738 | ||||||
chr6:122420796
|
C | T | 5 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+574C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420796 | ||||||
chr6:122420888
|
A | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.681+666A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122420888 | ||||||
chr6:122421048
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.681+826G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421048 | ||||||
chr6:122421230
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.682-920A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421230 | ||||||
chr6:122421239
|
C | T | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.682-911C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421239 | ||||||
chr6:122421439
|
G | GTAAGTGG others(18): Show |
18 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(15): Show | 24 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.682-709_682-685dup others(25): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 122421439 | |||||
chr6:122421808
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.682-342G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421808 | ||||||
chr6:122421820
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.682-330G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122421820 | ||||||
chr6:122422046
|
C | T | 5 | a0001c0001t0002g0014a0001c0001t0002g0081a0001c0001t0004g0014others(2): Show | 7 | HG02451.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-104C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122422046 | ||||||
chr6:122422048
|
A | T | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.682-102A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 7/12 | chr6 | 122422048 | ||||||
chr6:122422357
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.830+59T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422357 | ||||||
chr6:122422368
|
AC | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0160 | 5 | HG02027.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.830+71delC | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422368 | ||||||
chr6:122422541
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0030others(27): Show | 45 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.831-177A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422541 | ||||||
chr6:122422542
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.831-176A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422542 | ||||||
chr6:122422548
|
A | G | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.831-170A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422548 | ||||||
chr6:122422558
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.831-160A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422558 | ||||||
chr6:122422593
|
C | T | 10 | a0001c0001t0003g0217a0001c0002t0002g0010a0001c0002t0002g0023others(7): Show | 18 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.831-125C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422593 | ||||||
chr6:122422659
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831-59T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 8/12 | chr6 | 122422659 | ||||||
chr6:122423018
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1070+61C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423018 | ||||||
chr6:122423023
|
T | C | 9 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(6): Show | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.1070+66T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423023 | ||||||
chr6:122423043
|
T | G | 1 | a0001c0001t0001g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1070+86T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423043 | ||||||
chr6:122423062
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0124a0001c0001t0001g0128others(5): Show | 16 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1070+105T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423062 | ||||||
chr6:122423278
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0144a0001c0001t0003g0218 | 8 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1071-303C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423278 | ||||||
chr6:122423295
|
G | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071-286G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423295 | ||||||
chr6:122423357
|
G | A | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1071-224G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423357 | ||||||
chr6:122423565
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1071-16A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423565 | ||||||
chr6:122423566
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1071-15T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 9/12 | chr6 | 122423566 | ||||||
chr6:122423864
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1176+178A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122423864 | ||||||
chr6:122423898
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1176+212T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122423898 | ||||||
chr6:122423970
|
C | G | 1 | a0001c0001t0002g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1176+284C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122423970 | ||||||
chr6:122424284
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1176+598A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424284 | ||||||
chr6:122424457
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1176+771T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424457 | ||||||
chr6:122424505
|
A | G | 10 | a0001c0001t0003g0217a0001c0002t0002g0010a0001c0002t0002g0023others(7): Show | 18 | HG00544.hp1 HG02015.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1176+819A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424505 | ||||||
chr6:122424667
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1176+981A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424667 | ||||||
chr6:122424843
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1176+1157C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424843 | ||||||
chr6:122424989
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1176+1303T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122424989 | ||||||
chr6:122425259
|
A | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+1573A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425259 | ||||||
chr6:122425313
|
G | A | 17 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0018others(14): Show | 37 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1176+1627G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425313 | ||||||
chr6:122425333
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1176+1647C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425333 | ||||||
chr6:122425438
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1176+1752T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425438 | ||||||
chr6:122425621
|
G | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1176+1935G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425621 | ||||||
chr6:122425751
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1176+2065G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425751 | ||||||
chr6:122425768
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1176+2082A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425768 | ||||||
chr6:122425793
|
G | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1176+2107G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425793 | ||||||
chr6:122425860
|
A | T | 2 | a0001c0001t0003g0199a0001c0001t0003g0201 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1177-2043A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122425860 | ||||||
chr6:122426006
|
G | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 8 | NA18942.hp1 NA18950.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-1897G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426006 | ||||||
chr6:122426237
|
T | C | 2 | a0001c0001t0002g0077a0001c0001t0002g0220 | 2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1177-1666T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426237 | ||||||
chr6:122426371
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0005g0016 | 5 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177-1532C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426371 | ||||||
chr6:122426383
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1177-1520T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426383 | ||||||
chr6:122426469
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1177-1434C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426469 | ||||||
chr6:122426565
|
C | G | 4 | a0001c0001t0002g0007a0001c0001t0002g0061a0001c0001t0002g0072others(1): Show | 11 | HG02080.hp1 NA18942.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.1177-1338C>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426565 | ||||||
chr6:122426823
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1177-1080C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426823 | ||||||
chr6:122426969
|
G | A | 29 | a0001c0001t0001g0060a0001c0001t0002g0003a0001c0001t0002g0007others(26): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1177-934G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122426969 | ||||||
chr6:122427096
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1177-807C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427096 | ||||||
chr6:122427125
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1177-778T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427125 | ||||||
chr6:122427147
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1177-756A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427147 | ||||||
chr6:122427486
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-417G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427486 | ||||||
chr6:122427666
|
C | A | 9 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0042others(6): Show | 17 | HG00544.hp1 HG02015.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.1177-237C>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427666 | ||||||
chr6:122427718
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1177-185G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 10/12 | chr6 | 122427718 | ||||||
chr6:122428011
|
G | GTC | 35 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(32): Show | 56 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1230+56_1230+57dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 122428011 | |||||
chr6:122428098
|
T | G | 1 | a0001c0001t0002g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1230+142T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428098 | ||||||
chr6:122428228
|
G | T | 1 | a0001c0001t0002g0084 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1230+272G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428228 | ||||||
chr6:122428412
|
A | G | 33 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(30): Show | 53 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1230+456A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428412 | ||||||
chr6:122428505
|
G | A | 1 | a0001c0003t0002g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1230+549G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428505 | ||||||
chr6:122428748
|
A | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1230+792A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428748 | ||||||
chr6:122428931
|
A | G | 4 | a0001c0001t0002g0045a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1230+975A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122428931 | ||||||
chr6:122429122
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1230+1166A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429122 | ||||||
chr6:122429273
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0026 | 8 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1230+1317C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429273 | ||||||
chr6:122429828
|
T | G | 1 | a0001c0003t0002g0215 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1231-1602T>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429828 | ||||||
chr6:122429859
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1231-1571G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122429859 | ||||||
chr6:122430224
|
A | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1231-1206A>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430224 | ||||||
chr6:122430316
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 189 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1231-1114G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430316 | ||||||
chr6:122430664
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1231-766G>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430664 | ||||||
chr6:122430793
|
G | C | 1 | a0001c0001t0002g0040 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1231-637G>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122430793 | ||||||
chr6:122431042
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1231-388T>A | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431042 | ||||||
chr6:122431302
|
C | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0003g0002others(42): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1231-128C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431302 | ||||||
chr6:122431326
|
A | G | 34 | a0001c0001t0002g0002a0001c0001t0003g0002a0001c0001t0003g0022others(31): Show | 54 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1231-104A>G | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431326 | ||||||
chr6:122431405
|
T | TTA | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1231-15_1231-14dup others(2): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 122431405 | |||||
chr6:122431415
|
A | ATT | 6 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0001g0146others(3): Show | 6 | HG02027.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1231-9_1231-8dupTT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 122431415 | |||||
chr6:122431424
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG00423.hp1 | splice_region_variant&intron_variant | LOW | c.1231-6T>C | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 11/12 | chr6 | 122431424 | ||||||
chr6:122431559
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0166 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1315+45C>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | chr6 | 122431559 | ||||||
chr6:122431684
|
G | GT | 105 | a0001c0001t0001g0060a0001c0001t0001g0125a0001c0001t0001g0140others(102): Show | 177 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1315+182dupT | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 122431684 | |||||
chr6:122431684
|
G | GTT | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1315+181_1315+182d others(4): Show |
HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr6 | 122431684 | |||||
chr6:122431789
|
G | T | 1 | a0001c0001t0002g0091 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1316-136G>T | HSF2 | ENSG00000025156.13 | transcript | ENST00000368455.9 | protein_coding | 12/12 | chr6 | 122431789 |