geneid | 5612 |
---|---|
ensemblid | ENSG00000137492.9 |
hgncid | 9440 |
symbol | THAP12 |
name | THAP domain containing 12 |
refseq_nuc | NM_004705.4 |
refseq_prot | NP_004696.2 |
ensembl_nuc | ENST00000260045.8 |
ensembl_prot | ENSP00000260045.3 |
mane_status | MANE Select |
chr | chr11 |
start | 76349956 |
end | 76381132 |
strand | - |
ver | v1.2 |
region | chr11:76349956-76381132 |
region5000 | chr11:76344956-76386132 |
regionname0 | THAP12_chr11_76349956_76381132 |
regionname5000 | THAP12_chr11_76344956_76386132 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 761 | 354 | 75 | 65 | 155 | 13 | 44 | 119 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0002 | 0/0 | 761 | 26 | 0 | 3 | 22 | 1 | 0 | 17 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0003 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0004 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2286 | 350 | 71 | 65 | 155 | 13 | 44 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
c0002 | 0/0 | 2286 | 26 | 0 | 3 | 22 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
c0003 | 0/0 | 2286 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
c0004 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
c0005 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1205 | 364 | 65 | 68 | 172 | 14 | 43 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0002 | 0/0 | 1205 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0003 | 0/0 | 1205 | 4 | 0 | 0 | 4 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0004 | 0/0 | 1205 | 3 | 3 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0005 | 0/0 | 1205 | 3 | 3 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0006 | 0/0 | 1205 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0007 | 0/0 | 1205 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
t0008 | 0/0 | 1205 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0002 | 0/0 | 9 | 0 | 2 | 3 | 2 | 2 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0003 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0007 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0008 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0009 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0010 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2286 | 350 | 71 | 65 | 155 | 13 | 44 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0003 | 0/0 | 2286 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0002c0002 | 0/0 | 2286 | 26 | 0 | 3 | 22 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0003c0004 | 0/0 | 2286 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0004c0005 | 0/0 | 2286 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3490 | 334 | 60 | 65 | 151 | 13 | 43 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0001t0002 | 0/0 | 3490 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0001t0003 | 0/0 | 3490 | 4 | 0 | 0 | 4 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0001t0004 | 0/0 | 3490 | 3 | 3 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0001t0005 | 0/0 | 3490 | 3 | 3 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0001t0007 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0001t0008 | 0/0 | 3490 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0001c0003t0001 | 0/0 | 3490 | 4 | 4 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0002c0002t0001 | 0/0 | 3490 | 24 | 0 | 3 | 20 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0002c0002t0006 | 0/0 | 3490 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0003c0004t0001 | 0/0 | 3490 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
a0004c0005t0001 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | copy fasta | chr11 | 76344956 | 76386132 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 3 | 2 | 2 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0003 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0008 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0001t0008g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0002c0002t0006g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0003c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
a0004c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0047 | EUR | FIN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00558 | hp2 | a0002 | c0002 | t0006 | g0019 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02071 | hp1 | a0002 | c0002 | t0006 | g0019 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02080 | hp1 | a0003 | c0004 | t0001 | g0043 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02602 | hp2 | a0001 | c0001 | t0008 | g0289 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0058 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0056 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ASW | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ASW | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | GIH | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | THAP12_chr11_76344956_76386132 | THAP12 | chr11 | 76344956 | 76386132 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:76351745
|
C | G | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1405G>C | p.Val469Leu | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 1701/3490 | 1405/2286 | 469/761 | chr11 | 76351745 | ||
chr11:76352087
|
T | C | 1 | a0002 | 26 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(23): Show |
missense_variant | MODERATE | c.1063A>G | p.Ile355Val | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 1359/3490 | 1063/2286 | 355/761 | chr11 | 76352087 | ||
chr11:76380805
|
G | T | 1 | a0003 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.32C>A | p.Thr11Lys | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/5 | 328/3490 | 32/2286 | 11/761 | chr11 | 76380805 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:76352082
|
G | A | 2 | a0001c0003a0004c0005 | 5 | HG02559.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
synonymous_variant | LOW | c.1068C>T | p.Tyr356Tyr | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 1364/3490 | 1068/2286 | 356/761 | chr11 | 76352082 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:76350241
|
G | A | 1 | a0001c0001t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 623 | chr11 | 76350241 | |||||
chr11:76350368
|
G | A | 3 | a0001c0001t0002a0001c0001t0004a0001c0001t0005 | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*496C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 496 | chr11 | 76350368 | |||||
chr11:76350639
|
G | A | 1 | a0001c0001t0003 | 4 | NA18947.hp2 NA18955.hp2 NA18968.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*225C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 225 | chr11 | 76350639 | |||||
chr11:76350703
|
A | G | 1 | a0001c0001t0002 | 4 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*161T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 161 | chr11 | 76350703 | |||||
chr11:76350782
|
T | G | 1 | a0002c0002t0006 | 2 | HG00558.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*82A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 5/5 | 82 | chr11 | 76350782 | |||||
chr11:76380917
|
G | A | 1 | a0001c0001t0008 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/5 | 81 | chr11 | 76380917 | |||||
chr11:76381027
|
G | A | 1 | a0001c0001t0005 | 3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-191C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/5 | 191 | chr11 | 76381027 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:76352827
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0133a0001c0001t0001g0140 | 3 | NA18969.hp2 NA18992.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.356-33G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76352827 | ||||||
chr11:76352843
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.356-49G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76352843 | ||||||
chr11:76353073
|
C | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 349 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.356-279G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353073 | ||||||
chr11:76353222
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.356-428A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353222 | ||||||
chr11:76353574
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.356-780A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353574 | ||||||
chr11:76353869
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG00544.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.356-1075G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353869 | ||||||
chr11:76353870
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.356-1076C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353870 | ||||||
chr11:76353922
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.356-1128A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353922 | ||||||
chr11:76353964
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.356-1170C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76353964 | ||||||
chr11:76354003
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 86 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.356-1209G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354003 | ||||||
chr11:76354018
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.356-1224T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354018 | ||||||
chr11:76354023
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.356-1229G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354023 | ||||||
chr11:76354148
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(88): Show | 117 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.356-1354A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354148 | ||||||
chr11:76354163
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.356-1369C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354163 | ||||||
chr11:76354197
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.356-1403G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354197 | ||||||
chr11:76354318
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0191 | 3 | HG01243.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.355+1300A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354318 | ||||||
chr11:76354321
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0161 | 2 | NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.355+1297A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354321 | ||||||
chr11:76354380
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.355+1238C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354380 | ||||||
chr11:76354540
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.355+1078A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354540 | ||||||
chr11:76354749
|
G | A | 16 | a0002c0002t0001g0005a0002c0002t0001g0012a0002c0002t0001g0016others(13): Show | 26 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.355+869C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354749 | ||||||
chr11:76354770
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.355+848T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354770 | ||||||
chr11:76354927
|
A | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(34): Show | 46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.355+691T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354927 | ||||||
chr11:76354981
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+637C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76354981 | ||||||
chr11:76355092
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(34): Show | 46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.355+526C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 4/4 | chr11 | 76355092 | ||||||
chr11:76355666
|
G | GA | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-13dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76355666 | ||||||
chr11:76355706
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.319-52G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76355706 | ||||||
chr11:76356111
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.319-457T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356111 | ||||||
chr11:76356112
|
A | AAG | 34 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(31): Show | 44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.319-460_319-459dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356112 | ||||||
chr11:76356256
|
C | CT | 34 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(31): Show | 44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.319-603_319-602ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356256 | ||||||
chr11:76356337
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.319-683A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356337 | ||||||
chr11:76356388
|
C | T | 1 | a0002c0002t0001g0051 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.319-734G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356388 | ||||||
chr11:76356398
|
C | T | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | NA18612.hp1 NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.319-744G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356398 | ||||||
chr11:76356528
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.319-874C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356528 | ||||||
chr11:76356551
|
A | G | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.319-897T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356551 | ||||||
chr11:76356583
|
G | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.319-929C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356583 | ||||||
chr11:76356780
|
C | T | 3 | a0002c0002t0001g0050a0002c0002t0001g0052a0002c0002t0001g0059 | 3 | NA18940.hp2 NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.319-1126G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356780 | ||||||
chr11:76356937
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.319-1283C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76356937 | ||||||
chr11:76357423
|
T | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(58): Show | 87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.319-1769A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357423 | ||||||
chr11:76357510
|
ATT | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.319-1858_319-1857d others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357510 | ||||||
chr11:76357536
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(87): Show | 116 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.319-1882G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357536 | ||||||
chr11:76357812
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0081 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.319-2158G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357812 | ||||||
chr11:76357921
|
CA | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0240a0001c0001t0001g0265others(3): Show | 7 | HG01261.hp2 HG01358.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-2268delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357921 | ||||||
chr11:76357936
|
C | T | 6 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | HG00733.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-2282G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76357936 | ||||||
chr11:76358043
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.319-2389A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358043 | ||||||
chr11:76358053
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0221a0001c0001t0001g0244others(2): Show | 6 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-2399G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358053 | ||||||
chr11:76358164
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.319-2510T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358164 | ||||||
chr11:76358195
|
G | GA | 9 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0002g0099others(6): Show | 9 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-2542dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358195 | ||||||
chr11:76358195
|
GA | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(58): Show | 87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.319-2542delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358195 | ||||||
chr11:76358205
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.319-2551T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358205 | ||||||
chr11:76358233
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.319-2579G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358233 | ||||||
chr11:76358327
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.318+2629A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358327 | ||||||
chr11:76358362
|
T | C | 1 | a0002c0002t0001g0049 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.318+2594A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358362 | ||||||
chr11:76358479
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+2477A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358479 | ||||||
chr11:76358561
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+2395A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358561 | ||||||
chr11:76358620
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0179 | 3 | HG01175.hp1 HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.318+2336G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358620 | ||||||
chr11:76358817
|
C | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+2139G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358817 | ||||||
chr11:76358934
|
A | T | 1 | a0001c0001t0004g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.318+2022T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358934 | ||||||
chr11:76358971
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | HG01109.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.318+1985T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76358971 | ||||||
chr11:76359038
|
G | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+1918C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359038 | ||||||
chr11:76359314
|
T | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+1642A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359314 | ||||||
chr11:76359375
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0259 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.318+1581A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359375 | ||||||
chr11:76359409
|
G | A | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.318+1547C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359409 | ||||||
chr11:76359555
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.318+1401G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359555 | ||||||
chr11:76359576
|
C | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(33): Show | 47 | HG00609.hp2 HG00642.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.318+1380G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359576 | ||||||
chr11:76359654
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.318+1302G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359654 | ||||||
chr11:76359758
|
T | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0285 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.318+1198A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359758 | ||||||
chr11:76359831
|
G | GA | 34 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(31): Show | 44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.318+1124dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359831 | ||||||
chr11:76359832
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+1124T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359832 | ||||||
chr11:76359878
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0225a0001c0001t0001g0231others(2): Show | 7 | HG01074.hp2 HG01081.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1078T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359878 | ||||||
chr11:76359967
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0268 | 2 | HG00673.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.318+989T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76359967 | ||||||
chr11:76360029
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.318+927C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360029 | ||||||
chr11:76360060
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.318+896T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360060 | ||||||
chr11:76360090
|
T | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(58): Show | 87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.318+866A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360090 | ||||||
chr11:76360171
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.318+785A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360171 | ||||||
chr11:76360248
|
C | T | 3 | a0001c0001t0005g0290a0001c0001t0005g0291a0001c0001t0005g0292 | 3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.318+708G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360248 | ||||||
chr11:76360249
|
A | G | 1 | a0002c0002t0001g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.318+707T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360249 | ||||||
chr11:76360323
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.318+633T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360323 | ||||||
chr11:76360328
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.318+628A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360328 | ||||||
chr11:76360428
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.318+528C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360428 | ||||||
chr11:76360691
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.318+265C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 3/4 | chr11 | 76360691 | ||||||
chr11:76361498
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.211-435C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76361498 | ||||||
chr11:76361749
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.211-686A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76361749 | ||||||
chr11:76362352
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0088a0001c0001t0001g0090others(1): Show | 4 | NA18949.hp2 NA19000.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1289C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362352 | ||||||
chr11:76362387
|
A | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(34): Show | 46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.211-1324T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362387 | ||||||
chr11:76362541
|
G | A | 1 | a0002c0002t0001g0047 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.211-1478C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362541 | ||||||
chr11:76362795
|
G | C | 1 | a0001c0001t0004g0094 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211-1732C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362795 | ||||||
chr11:76362828
|
G | GA | 4 | a0001c0001t0002g0098a0001c0001t0004g0093a0001c0001t0004g0094others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1766dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362828 | ||||||
chr11:76362998
|
C | T | 1 | a0002c0002t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.211-1935G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76362998 | ||||||
chr11:76363013
|
T | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1950A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363013 | ||||||
chr11:76363048
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.211-1985C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363048 | ||||||
chr11:76363056
|
T | C | 22 | a0001c0001t0001g0213a0001c0003t0001g0046a0001c0003t0001g0054others(19): Show | 32 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.211-1993A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363056 | ||||||
chr11:76363072
|
G | C | 1 | a0001c0001t0007g0248 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211-2009C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363072 | ||||||
chr11:76363076
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.211-2013C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363076 | ||||||
chr11:76363149
|
A | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 167 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.211-2086T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363149 | ||||||
chr11:76363473
|
A | T | 1 | a0001c0001t0001g0209 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.210+2379T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363473 | ||||||
chr11:76363496
|
A | C | 1 | a0001c0003t0001g0054 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.210+2356T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363496 | ||||||
chr11:76363558
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.210+2294A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363558 | ||||||
chr11:76363562
|
G | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0165 | 4 | NA18947.hp2 NA18955.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+2290C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363562 | ||||||
chr11:76363571
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.210+2281T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363571 | ||||||
chr11:76363572
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.210+2280A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363572 | ||||||
chr11:76363589
|
T | TTTTG | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(173): Show | 234 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.210+2259_210+2262d others(6): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363589 | ||||||
chr11:76363589
|
T | TTTTGTTT others(1): Show |
89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(86): Show | 115 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.210+2255_210+2262d others(10): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363589 | ||||||
chr11:76363625
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+2227C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363625 | ||||||
chr11:76363757
|
T | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(93): Show | 123 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.210+2095A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363757 | ||||||
chr11:76363760
|
T | G | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.210+2092A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363760 | ||||||
chr11:76363845
|
A | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+2007T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363845 | ||||||
chr11:76363848
|
T | G | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+2004A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363848 | ||||||
chr11:76363851
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.210+2001G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363851 | ||||||
chr11:76363970
|
C | G | 13 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(10): Show | 13 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.210+1882G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76363970 | ||||||
chr11:76364064
|
A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(32): Show | 44 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.210+1788T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364064 | ||||||
chr11:76364065
|
T | C | 4 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 4 | HG01099.hp2 HG01346.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+1787A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364065 | ||||||
chr11:76364099
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.210+1753C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364099 | ||||||
chr11:76364629
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.210+1223G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364629 | ||||||
chr11:76364691
|
T | C | 1 | a0001c0001t0005g0291 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.210+1161A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76364691 | ||||||
chr11:76365141
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.210+711G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365141 | ||||||
chr11:76365142
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.210+710C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365142 | ||||||
chr11:76365251
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.210+601C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365251 | ||||||
chr11:76365292
|
T | TA | 26 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0102others(23): Show | 38 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.210+559dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365292 | ||||||
chr11:76365292
|
TA | T | 15 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0132others(12): Show | 15 | HG00323.hp1 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.210+559delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365292 | ||||||
chr11:76365293
|
A | T | 1 | a0001c0001t0001g0196 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.210+559T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365293 | ||||||
chr11:76365356
|
A | AGTTTT | 6 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0156others(3): Show | 11 | HG00733.hp2 HG01192.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+491_210+495dup others(5): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365356 | ||||||
chr11:76365394
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.210+458A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365394 | ||||||
chr11:76365407
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210+445G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365407 | ||||||
chr11:76365496
|
A | G | 3 | a0002c0002t0001g0012a0002c0002t0001g0048a0002c0002t0001g0049 | 5 | NA18955.hp1 NA18992.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+356T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365496 | ||||||
chr11:76365515
|
C | T | 5 | a0001c0001t0001g0236a0001c0001t0001g0250a0001c0001t0001g0251others(2): Show | 5 | HG00733.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+337G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365515 | ||||||
chr11:76365573
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210+279C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365573 | ||||||
chr11:76365736
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.210+116C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365736 | ||||||
chr11:76365749
|
G | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+103C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365749 | ||||||
chr11:76365798
|
T | TGA | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+52_210+53dupTC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 2/4 | chr11 | 76365798 | ||||||
chr11:76366100
|
G | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-128C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366100 | ||||||
chr11:76366276
|
A | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(59): Show | 88 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.90-304T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366276 | ||||||
chr11:76366457
|
A | G | 34 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(31): Show | 44 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.90-485T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366457 | ||||||
chr11:76366573
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.90-601G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366573 | ||||||
chr11:76366629
|
C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(32): Show | 44 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.90-657G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366629 | ||||||
chr11:76366675
|
C | T | 1 | a0001c0001t0004g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.90-703G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366675 | ||||||
chr11:76366682
|
G | GA | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0152others(5): Show | 8 | HG01261.hp2 HG02055.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.90-711dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76366682 | ||||||
chr11:76367081
|
C | CT | 7 | a0001c0001t0001g0104a0001c0001t0001g0116a0001c0001t0001g0128others(4): Show | 7 | HG00597.hp2 NA18948.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.90-1110dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367081 | ||||||
chr11:76367081
|
C | CTT | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(34): Show | 46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.90-1111_90-1110dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367081 | ||||||
chr11:76367085
|
T | C | 3 | a0001c0001t0005g0290a0001c0001t0005g0291a0001c0001t0005g0292 | 3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.90-1113A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367085 | ||||||
chr11:76367234
|
G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-1262C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367234 | ||||||
chr11:76367303
|
C | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-1331G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367303 | ||||||
chr11:76367563
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 167 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.90-1591A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367563 | ||||||
chr11:76367595
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.90-1623C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367595 | ||||||
chr11:76367715
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.90-1743C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367715 | ||||||
chr11:76367820
|
C | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 86 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.90-1848G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367820 | ||||||
chr11:76367965
|
TAC | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-1995_90-1994del others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367965 | ||||||
chr11:76367994
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0186 | 2 | NA18987.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.90-2022A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76367994 | ||||||
chr11:76368112
|
G | C | 10 | a0002c0002t0001g0012a0002c0002t0001g0016a0002c0002t0001g0017others(7): Show | 14 | HG00323.hp2 NA18940.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.90-2140C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368112 | ||||||
chr11:76368136
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.90-2164G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368136 | ||||||
chr11:76368237
|
A | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 349 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.90-2265T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368237 | ||||||
chr11:76368300
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.90-2328A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368300 | ||||||
chr11:76368674
|
C | A | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-2702G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368674 | ||||||
chr11:76368728
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.90-2756G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76368728 | ||||||
chr11:76369022
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(93): Show | 123 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.90-3050T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369022 | ||||||
chr11:76369090
|
G | C | 2 | a0001c0001t0001g0181a0003c0004t0001g0043 | 2 | HG00673.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.90-3118C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369090 | ||||||
chr11:76369162
|
T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(32): Show | 44 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.90-3190A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369162 | ||||||
chr11:76369211
|
A | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0213a0001c0001t0001g0218others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-3239T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369211 | ||||||
chr11:76369232
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.90-3260C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369232 | ||||||
chr11:76369486
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.90-3514C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369486 | ||||||
chr11:76369604
|
A | G | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3632T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369604 | ||||||
chr11:76369630
|
A | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3658T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369630 | ||||||
chr11:76369631
|
GC | G | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3660delG | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369631 | ||||||
chr11:76369634
|
C | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3662G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369634 | ||||||
chr11:76369635
|
A | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3663T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369635 | ||||||
chr11:76369636
|
C | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3664G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369636 | ||||||
chr11:76369637
|
C | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-3665G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369637 | ||||||
chr11:76369699
|
G | A | 1 | a0001c0001t0001g0025 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.90-3727C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369699 | ||||||
chr11:76369846
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.90-3874C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369846 | ||||||
chr11:76369922
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0166 | 3 | HG02602.hp1 HG02735.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.90-3950T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76369922 | ||||||
chr11:76370050
|
G | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0076others(1): Show | 5 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-4078C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370050 | ||||||
chr11:76370151
|
C | T | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-4179G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370151 | ||||||
chr11:76370203
|
A | G | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-4231T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370203 | ||||||
chr11:76370353
|
G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-4381C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370353 | ||||||
chr11:76370358
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.90-4386A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370358 | ||||||
chr11:76370358
|
TG | T | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(56): Show | 85 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.90-4387delC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370358 | ||||||
chr11:76370359
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0160 | 2 | NA18966.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.90-4387C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370359 | ||||||
chr11:76370365
|
T | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0160 | 2 | NA18966.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.90-4393A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370365 | ||||||
chr11:76370369
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0160 | 2 | NA18966.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.90-4397C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370369 | ||||||
chr11:76370746
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.90-4774G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370746 | ||||||
chr11:76370830
|
G | GA | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(100): Show | 145 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.90-4859dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370830 | ||||||
chr11:76370835
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.90-4863T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370835 | ||||||
chr11:76370841
|
A | AAT | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(40): Show | 70 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.90-4870_90-4869ins others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | ||||||
chr11:76370841
|
A | AATAT | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0154others(7): Show | 10 | HG01175.hp1 HG01978.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-4870_90-4869ins others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | ||||||
chr11:76370841
|
A | AT | 9 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0122others(6): Show | 9 | HG00323.hp1 HG01069.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-4870_90-4869ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | ||||||
chr11:76370841
|
A | T | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0148others(2): Show | 5 | HG02602.hp1 HG03516.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-4869T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370841 | ||||||
chr11:76370843
|
A | AAT | 14 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0083others(11): Show | 14 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.90-4873_90-4872dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370843 | ||||||
chr11:76370843
|
A | AT | 24 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0170others(21): Show | 28 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.90-4872_90-4871ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370843 | ||||||
chr11:76370843
|
A | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(92): Show | 133 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.90-4871T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370843 | ||||||
chr11:76370845
|
T | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0249 | 2 | HG01192.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.90-4873A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370845 | ||||||
chr11:76370879
|
A | G | 2 | a0002c0002t0001g0018a0002c0002t0006g0019 | 4 | HG00558.hp2 HG02071.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-4907T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370879 | ||||||
chr11:76370883
|
G | A | 2 | a0002c0002t0001g0018a0002c0002t0006g0019 | 4 | HG00558.hp2 HG02071.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-4911C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370883 | ||||||
chr11:76370884
|
T | TATTC | 19 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(16): Show | 27 | HG00323.hp2 HG00544.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.90-4916_90-4913dup others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370884 | ||||||
chr11:76370884
|
T | TTC | 2 | a0002c0002t0001g0018a0002c0002t0006g0019 | 4 | HG00558.hp2 HG02071.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-4913_90-4912ins others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370884 | ||||||
chr11:76370997
|
G | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-5025C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76370997 | ||||||
chr11:76371018
|
A | G | 4 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 4 | HG01099.hp2 HG01346.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-5046T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371018 | ||||||
chr11:76371096
|
C | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.90-5124G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371096 | ||||||
chr11:76371233
|
T | C | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-5261A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371233 | ||||||
chr11:76371298
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(11): Show | 17 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.90-5326C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371298 | ||||||
chr11:76371311
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0156others(4): Show | 12 | HG00733.hp2 HG00735.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-5339G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371311 | ||||||
chr11:76371336
|
T | G | 10 | a0001c0001t0001g0038a0001c0001t0001g0213a0001c0001t0001g0218others(7): Show | 11 | HG00639.hp1 HG01074.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.90-5364A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371336 | ||||||
chr11:76371461
|
T | C | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02056.hp1 NA18952.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.90-5489A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371461 | ||||||
chr11:76371661
|
CTTG | C | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-5692_90-5690del others(3): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371661 | ||||||
chr11:76371688
|
CCAAGGAG others(1): Show |
C | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.90-5724_90-5717del others(8): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371688 | ||||||
chr11:76371710
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.90-5738G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371710 | ||||||
chr11:76371810
|
CT | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 325 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.90-5839delA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371810 | ||||||
chr11:76371895
|
C | T | 10 | a0002c0002t0001g0012a0002c0002t0001g0016a0002c0002t0001g0017others(7): Show | 14 | HG00323.hp2 NA18940.hp2 NA18941.hp2 others(11): Show |
intron_variant | MODIFIER | c.90-5923G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371895 | ||||||
chr11:76371919
|
T | G | 1 | a0001c0001t0001g0219 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.90-5947A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76371919 | ||||||
chr11:76372091
|
G | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(58): Show | 87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90-6119C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372091 | ||||||
chr11:76372205
|
A | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 347 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(344): Show |
intron_variant | MODIFIER | c.90-6233T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372205 | ||||||
chr11:76372275
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.90-6303G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372275 | ||||||
chr11:76372389
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0150 | 2 | HG02135.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.90-6417A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372389 | ||||||
chr11:76372407
|
T | TA | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 344 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(341): Show |
intron_variant | MODIFIER | c.90-6436dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372407 | ||||||
chr11:76372449
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.90-6477C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372449 | ||||||
chr11:76372527
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 167 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.90-6555T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372527 | ||||||
chr11:76372588
|
T | TA | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.90-6617_90-6616ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372588 | ||||||
chr11:76372589
|
T | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-6617A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372589 | ||||||
chr11:76372589
|
TA | T | 24 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0067others(21): Show | 25 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.90-6618delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372589 | ||||||
chr11:76372656
|
C | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0221a0001c0001t0001g0244others(2): Show | 6 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-6684G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372656 | ||||||
chr11:76372701
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.90-6729A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372701 | ||||||
chr11:76372774
|
C | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(58): Show | 87 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.90-6802G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372774 | ||||||
chr11:76372887
|
C | CA | 7 | a0001c0001t0001g0039a0001c0001t0001g0214a0001c0001t0001g0240others(4): Show | 8 | HG01261.hp2 HG01358.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-6916dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76372887 | ||||||
chr11:76373147
|
TCCAGCCT others(364): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.89+7230_90-7176del | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373147 | ||||||
chr11:76373191
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 373 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(370): Show |
intron_variant | MODIFIER | c.90-7219A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373191 | ||||||
chr11:76373217
|
G | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-7245C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373217 | ||||||
chr11:76373343
|
C | CA | 11 | a0001c0001t0001g0022a0001c0001t0001g0091a0001c0001t0001g0106others(8): Show | 12 | HG00642.hp2 HG00673.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-7372dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373343 | ||||||
chr11:76373371
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.89+7377A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373371 | ||||||
chr11:76373380
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89+7368A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373380 | ||||||
chr11:76373489
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89+7259C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373489 | ||||||
chr11:76373650
|
T | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 349 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.89+7098A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373650 | ||||||
chr11:76373718
|
C | CA | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 368 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(365): Show |
intron_variant | MODIFIER | c.89+7029dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373718 | ||||||
chr11:76373775
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.89+6973G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373775 | ||||||
chr11:76373873
|
A | T | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.89+6875T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76373873 | ||||||
chr11:76374141
|
A | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.89+6607T>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374141 | ||||||
chr11:76374215
|
C | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 349 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.89+6533G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374215 | ||||||
chr11:76374386
|
C | CA | 9 | a0001c0001t0001g0042a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG02080.hp2 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.89+6361dupT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374386 | ||||||
chr11:76374386
|
CA | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 94 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.89+6361delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374386 | ||||||
chr11:76374386
|
CAA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(112): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.89+6360_89+6361del others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374386 | ||||||
chr11:76374622
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.89+6126G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374622 | ||||||
chr11:76374636
|
G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+6112C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374636 | ||||||
chr11:76374683
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.89+6065T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374683 | ||||||
chr11:76374752
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.89+5996A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374752 | ||||||
chr11:76374798
|
G | A | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+5950C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374798 | ||||||
chr11:76374812
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.89+5936A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374812 | ||||||
chr11:76374892
|
C | CT | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+5855dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76374892 | ||||||
chr11:76375061
|
G | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0259 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.89+5687C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375061 | ||||||
chr11:76375070
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.89+5678A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375070 | ||||||
chr11:76375169
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.89+5579A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375169 | ||||||
chr11:76375235
|
A | T | 1 | a0001c0001t0001g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.89+5513T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375235 | ||||||
chr11:76375390
|
C | CT | 18 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0090others(15): Show | 18 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.89+5357dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375390 | ||||||
chr11:76375393
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00408.hp2 HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.89+5355A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375393 | ||||||
chr11:76375747
|
T | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0126others(1): Show | 5 | HG00621.hp2 HG02080.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+5001A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | ||||||
chr11:76375747
|
T | TG | 38 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0024others(35): Show | 49 | HG00621.hp1 HG01168.hp1 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.89+5000dupC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | ||||||
chr11:76375747
|
T | TGG | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 128 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.89+4999_89+5000dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | ||||||
chr11:76375747
|
T | TGGG | 74 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(71): Show | 99 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.89+4998_89+5000dup others(3): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | ||||||
chr11:76375747
|
T | TGGGG | 20 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0090others(17): Show | 22 | HG00733.hp1 HG01123.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.89+4997_89+5000dup others(4): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | ||||||
chr11:76375747
|
TG | T | 27 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(24): Show | 37 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.89+5000delC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375747 | ||||||
chr11:76375756
|
G | GT | 2 | a0001c0001t0001g0027a0001c0001t0001g0126 | 3 | NA18988.hp1 NA19070.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.89+4991_89+4992ins others(1): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375756 | ||||||
chr11:76375849
|
T | C | 1 | a0001c0001t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.89+4899A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375849 | ||||||
chr11:76375994
|
T | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+4754A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76375994 | ||||||
chr11:76376187
|
G | A | 3 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095 | 3 | HG02622.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89+4561C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376187 | ||||||
chr11:76376322
|
A | T | 1 | a0001c0001t0004g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89+4426T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376322 | ||||||
chr11:76376355
|
T | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 91 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.89+4393A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376355 | ||||||
chr11:76376456
|
A | T | 1 | a0001c0001t0004g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.89+4292T>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376456 | ||||||
chr11:76376498
|
G | C | 1 | a0001c0001t0004g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.89+4250C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376498 | ||||||
chr11:76376615
|
G | GT | 10 | a0001c0001t0001g0004a0001c0001t0001g0206a0001c0001t0001g0264others(7): Show | 15 | HG01261.hp2 HG01358.hp1 HG03453.hp1 others(12): Show |
intron_variant | MODIFIER | c.89+4132dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376615 | ||||||
chr11:76376615
|
G | GTT | 59 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(56): Show | 79 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.89+4131_89+4132dup others(2): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376615 | ||||||
chr11:76376615
|
G | GTTT | 19 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0208others(16): Show | 20 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.89+4130_89+4132dup others(3): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376615 | ||||||
chr11:76376623
|
TG | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 20 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.89+4124delC | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376623 | ||||||
chr11:76376624
|
G | GT | 13 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(10): Show | 13 | HG02055.hp1 HG02080.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.89+4123dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376624 | ||||||
chr11:76376624
|
G | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(89): Show | 118 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.89+4124C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376624 | ||||||
chr11:76376624
|
GT | G | 47 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(44): Show | 58 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.89+4123delA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376624 | ||||||
chr11:76376711
|
G | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.89+4037C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376711 | ||||||
chr11:76376748
|
T | TCTAAACA others(319): Show |
2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.89+3999_89+4000ins others(326): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376748 | ||||||
chr11:76376748
|
T | TCTAAACA others(320): Show |
1 | a0001c0001t0001g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.89+3999_89+4000ins others(327): Show |
THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376748 | ||||||
chr11:76376800
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(34): Show | 46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.89+3948G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76376800 | ||||||
chr11:76377044
|
C | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+3704G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377044 | ||||||
chr11:76377183
|
T | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+3565A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377183 | ||||||
chr11:76377823
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.89+2925G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377823 | ||||||
chr11:76377860
|
G | A | 1 | a0002c0002t0001g0059 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.89+2888C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377860 | ||||||
chr11:76377884
|
C | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+2864G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377884 | ||||||
chr11:76377939
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.89+2809G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76377939 | ||||||
chr11:76378198
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.89+2550G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378198 | ||||||
chr11:76378252
|
T | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+2496A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378252 | ||||||
chr11:76378256
|
TA | T | 10 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(7): Show | 10 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+2491delT | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378256 | ||||||
chr11:76378406
|
C | G | 3 | a0001c0001t0005g0290a0001c0001t0005g0291a0001c0001t0005g0292 | 3 | HG02818.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.89+2342G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378406 | ||||||
chr11:76378510
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.89+2238T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378510 | ||||||
chr11:76378598
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.89+2150G>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378598 | ||||||
chr11:76378724
|
G | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(88): Show | 117 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.89+2024C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378724 | ||||||
chr11:76378839
|
C | T | 3 | a0001c0001t0004g0093a0001c0001t0004g0094a0001c0001t0004g0095 | 3 | HG02622.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89+1909G>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76378839 | ||||||
chr11:76379026
|
T | A | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | NA18612.hp2 NA18966.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+1722A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379026 | ||||||
chr11:76379041
|
G | A | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | NA18612.hp1 NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.89+1707C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379041 | ||||||
chr11:76379130
|
T | C | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.89+1618A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379130 | ||||||
chr11:76379195
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.89+1553T>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379195 | ||||||
chr11:76379245
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.89+1503A>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379245 | ||||||
chr11:76379544
|
G | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0280a0001c0001t0001g0281 | 4 | NA18950.hp2 NA18982.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+1204C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379544 | ||||||
chr11:76379618
|
G | C | 1 | a0001c0001t0001g0042 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.89+1130C>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379618 | ||||||
chr11:76379645
|
T | C | 1 | a0002c0002t0001g0060 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.89+1103A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379645 | ||||||
chr11:76379799
|
G | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0020others(34): Show | 46 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.89+949C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379799 | ||||||
chr11:76379894
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.89+854A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379894 | ||||||
chr11:76379921
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.89+827A>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76379921 | ||||||
chr11:76380049
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.89+699A>G | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380049 | ||||||
chr11:76380083
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.89+665C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380083 | ||||||
chr11:76380245
|
A | AT | 21 | a0001c0003t0001g0046a0001c0003t0001g0054a0001c0003t0001g0056others(18): Show | 31 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.89+502dupA | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380245 | ||||||
chr11:76380407
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.89+341G>C | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380407 | ||||||
chr11:76380444
|
G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG02922.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.89+304C>T | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380444 | ||||||
chr11:76380715
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.89+33C>A | THAP12 | ENSG00000137492.9 | transcript | ENST00000260045.8 | protein_coding | 1/4 | chr11 | 76380715 |