geneid | 51078 |
---|---|
ensemblid | ENSG00000176946.13 |
hgncid | 23187 |
symbol | THAP4 |
name | THAP domain containing 4 |
refseq_nuc | NM_015963.6 |
refseq_prot | NP_057047.4 |
ensembl_nuc | ENST00000407315.6 |
ensembl_prot | ENSP00000385006.1 |
mane_status | MANE Select |
chr | chr2 |
start | 241584405 |
end | 241637158 |
strand | - |
ver | v1.2 |
region | chr2:241584405-241637158 |
region5000 | chr2:241579405-241642158 |
regionname0 | THAP4_chr2_241584405_241637158 |
regionname5000 | THAP4_chr2_241579405_241642158 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 577 | 274 | 52 | 36 | 157 | 5 | 23 | 124 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002 | 1/0 | 577 | 112 | 41 | 26 | 20 | 9 | 15 | 14 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0003 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0004 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0005 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0006 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1734 | 139 | 36 | 25 | 68 | 3 | 6 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0002 | 0/0 | 1734 | 134 | 16 | 11 | 89 | 2 | 16 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0003 | 1/0 | 1734 | 75 | 23 | 17 | 14 | 9 | 11 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0004 | 0/0 | 1734 | 33 | 14 | 9 | 6 | 0 | 4 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0005 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0006 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0007 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0008 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0009 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0010 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
c0011 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 343 | 375 | 92 | 58 | 172 | 14 | 37 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
t0002 | 0/0 | 343 | 6 | 1 | 2 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
t0003 | 0/0 | 343 | 5 | 0 | 4 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
t0004 | 0/0 | 351 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
t0005 | 0/0 | 343 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0018 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1734 | 139 | 36 | 25 | 68 | 3 | 6 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0001c0002 | 0/0 | 1734 | 134 | 16 | 11 | 89 | 2 | 16 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0001c0009 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0003 | 1/0 | 1734 | 75 | 23 | 17 | 14 | 9 | 11 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0004 | 0/0 | 1734 | 33 | 14 | 9 | 6 | 0 | 4 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0005 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0006 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0003c0007 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0004c0011 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0005c0010 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0006c0008 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2076 | 134 | 36 | 23 | 65 | 3 | 6 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0001c0001t0002 | 0/0 | 2076 | 5 | 0 | 2 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0001c0002t0001 | 0/0 | 2076 | 131 | 16 | 11 | 86 | 2 | 16 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0001c0002t0004 | 0/0 | 2084 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0001c0009t0001 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0003t0001 | 1/0 | 2076 | 74 | 22 | 17 | 14 | 9 | 11 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0003t0002 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0004t0001 | 0/0 | 2076 | 27 | 13 | 5 | 6 | 0 | 3 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0004t0003 | 0/0 | 2076 | 5 | 0 | 4 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0004t0005 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0005t0001 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0002c0006t0001 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0003c0007t0001 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0004c0011t0001 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0005c0010t0001 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
a0006c0008t0001 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | copy fasta | chr2 | 241579405 | 241642158 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0018 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0002t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0001c0009t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0004t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0002c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0003c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0004c0011t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0005c0010t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
a0006c0008t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0088 | EUR | GBR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0299 | EUR | GBR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00280 | hp1 | a0002 | c0003 | t0001 | g0195 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0092 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00544 | hp1 | a0002 | c0004 | t0001 | g0166 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0084 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00642 | hp1 | a0002 | c0004 | t0001 | g0238 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0090 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0102 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG00741 | hp2 | a0002 | c0003 | t0001 | g0099 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0091 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01081 | hp1 | a0002 | c0004 | t0003 | g0158 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0263 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01106 | hp2 | a0006 | c0008 | t0001 | g0074 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01167 | hp1 | a0002 | c0004 | t0001 | g0078 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01168 | hp2 | a0002 | c0003 | t0001 | g0192 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01169 | hp1 | a0002 | c0004 | t0001 | g0075 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0182 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0184 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0181 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01243 | hp2 | a0002 | c0004 | t0001 | g0164 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0087 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01258 | hp1 | a0002 | c0003 | t0001 | g0180 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01261 | hp1 | a0002 | c0003 | t0001 | g0093 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01261 | hp2 | a0002 | c0004 | t0003 | g0163 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01346 | hp1 | a0004 | c0011 | t0001 | g0237 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0011 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0011 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0016 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01884 | hp1 | a0002 | c0003 | t0002 | g0262 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01891 | hp1 | a0002 | c0004 | t0001 | g0278 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01891 | hp2 | a0002 | c0006 | t0001 | g0156 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0175 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0324 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01952 | hp1 | a0002 | c0003 | t0001 | g0174 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01993 | hp1 | a0002 | c0003 | t0001 | g0186 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02004 | hp2 | a0002 | c0004 | t0003 | g0162 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0101 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02056 | hp2 | a0002 | c0003 | t0001 | g0258 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0346 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02129 | hp1 | a0005 | c0010 | t0001 | g0035 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02129 | hp2 | a0002 | c0003 | t0001 | g0188 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02135 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02258 | hp1 | a0003 | c0007 | t0001 | g0073 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02293 | hp2 | a0002 | c0004 | t0001 | g0280 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02451 | hp1 | a0002 | c0004 | t0001 | g0161 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0081 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02523 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02572 | hp1 | a0002 | c0004 | t0001 | g0170 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0094 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02602 | hp1 | a0001 | c0009 | t0001 | g0337 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0100 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02615 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0265 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0077 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02647 | hp1 | a0002 | c0003 | t0001 | g0089 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0266 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0183 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02717 | hp1 | a0002 | c0003 | t0001 | g0095 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0098 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02738 | hp1 | a0002 | c0004 | t0001 | g0171 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0342 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02818 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0267 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02886 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0196 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02965 | hp1 | a0002 | c0003 | t0001 | g0179 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02965 | hp2 | a0002 | c0003 | t0001 | g0172 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02970 | hp2 | a0002 | c0003 | t0001 | g0020 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0068 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0177 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0302 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03130 | hp2 | a0002 | c0004 | t0001 | g0072 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03139 | hp1 | a0002 | c0006 | t0001 | g0155 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03209 | hp1 | a0002 | c0004 | t0005 | g0350 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03239 | hp1 | a0002 | c0004 | t0001 | g0165 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03453 | hp2 | a0002 | c0005 | t0001 | g0154 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03490 | hp1 | a0002 | c0004 | t0003 | g0160 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0317 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0261 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0289 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0318 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0169 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03540 | hp1 | a0002 | c0004 | t0001 | g0279 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03540 | hp2 | a0002 | c0004 | t0001 | g0157 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03579 | hp1 | a0002 | c0003 | t0001 | g0020 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03579 | hp2 | a0002 | c0004 | t0001 | g0061 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03654 | hp2 | a0002 | c0003 | t0001 | g0176 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03704 | hp1 | a0002 | c0003 | t0001 | g0024 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0314 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0300 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03834 | hp1 | a0002 | c0003 | t0001 | g0086 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0328 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0097 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04115 | hp1 | a0002 | c0004 | t0001 | g0277 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0321 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0320 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0361 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04204 | hp1 | a0002 | c0003 | t0001 | g0242 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0085 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18939 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0187 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0335 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18945 | hp2 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18972 | hp2 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18974 | hp1 | a0001 | c0002 | t0004 | g0362 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18977 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0363 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18998 | hp2 | a0002 | c0004 | t0001 | g0167 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18999 | hp1 | a0002 | c0004 | t0001 | g0080 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19000 | hp2 | a0002 | c0004 | t0001 | g0168 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19043 | hp1 | a0002 | c0004 | t0001 | g0021 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19055 | hp1 | a0001 | c0002 | t0004 | g0364 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19055 | hp2 | a0002 | c0004 | t0001 | g0076 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ASW | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0264 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0185 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0083 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0201 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0104 | SAS | GIH | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | GIH | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01123 | hp1 | a0002 | c0004 | t0003 | g0159 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02109 | hp1 | a0002 | c0003 | t0001 | g0096 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0343 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG02559 | hp2 | a0002 | c0003 | t0001 | g0260 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG03471 | hp2 | a0002 | c0005 | t0001 | g0153 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0173 | AFR | USA | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | USA | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0359 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
NA21309 | hp2 | a0002 | c0003 | t0001 | g0082 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0001 | g0178 | REF | REF | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241601937
|
T | C | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.1573A>G | p.Ile525Val | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/6 | 1714/2076 | 1573/1734 | 525/577 | chr2 | 241601937 | ||
chr2:241633535
|
C | G | 1 | a0006 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.622G>C | p.Gly208Arg | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 763/2076 | 622/1734 | 208/577 | chr2 | 241633535 | ||
chr2:241633596
|
C | A | 1 | a0004 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.561G>T | p.Gln187His | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 702/2076 | 561/1734 | 187/577 | chr2 | 241633596 | ||
chr2:241633796
|
T | C | 3 | a0001a0004a0005 | 276 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(273): Show |
missense_variant | MODERATE | c.361A>G | p.Ser121Gly | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 502/2076 | 361/1734 | 121/577 | chr2 | 241633796 | ||
chr2:241633807
|
C | T | 1 | a0003 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.350G>A | p.Ser117Asn | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 491/2076 | 350/1734 | 117/577 | chr2 | 241633807 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241603055
|
C | T | 1 | a0001c0009 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1425G>A | p.Thr475Thr | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/6 | 1566/2076 | 1425/1734 | 475/577 | chr2 | 241603055 | ||
chr2:241633278
|
C | T | 1 | a0002c0006 | 2 | HG01891.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.879G>A | p.Pro293Pro | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 1020/2076 | 879/1734 | 293/577 | chr2 | 241633278 | ||
chr2:241633284
|
C | T | 1 | a0002c0005 | 2 | HG03453.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.873G>A | p.Ala291Ala | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 1014/2076 | 873/1734 | 291/577 | chr2 | 241633284 | ||
chr2:241633431
|
A | G | 5 | a0001c0002a0001c0009a0002c0004others(2): Show | 172 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(169): Show |
synonymous_variant | LOW | c.726T>C | p.Ser242Ser | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 867/2076 | 726/1734 | 242/577 | chr2 | 241633431 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241584508
|
C | G | 1 | a0002c0004t0003 | 5 | HG01081.hp1 HG01123.hp1 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*98G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 6/6 | 98 | chr2 | 241584508 | |||||
chr2:241584527
|
C | T | 1 | a0002c0004t0005 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 6/6 | 79 | chr2 | 241584527 | |||||
chr2:241584528
|
G | A | 2 | a0001c0001t0002a0002c0003t0002 | 6 | HG01884.hp1 HG01981.hp1 HG02293.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*78C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 6/6 | 78 | chr2 | 241584528 | |||||
chr2:241637059
|
G | GCCGCCCG others(1): Show |
1 | a0001c0002t0004 | 3 | NA18974.hp1 NA18981.hp1 NA19055.hp1 |
5_prime_UTR_variant | MODIFIER | c.-50_-43dupGCGGGCGG | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/6 | 43 | chr2 | 241637059 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241584991
|
C | T | 4 | a0001c0002t0001g0026a0001c0002t0004g0362a0001c0002t0004g0363others(1): Show | 4 | NA18974.hp1 NA18981.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-266G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241584991 | ||||||
chr2:241585172
|
G | A | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1615-447C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585172 | ||||||
chr2:241585241
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1615-516C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585241 | ||||||
chr2:241585279
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0039a0002c0003t0001g0180 | 3 | HG01258.hp1 HG02080.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1615-554G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585279 | ||||||
chr2:241585498
|
A | G | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0002c0004t0001g0075others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-773T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585498 | ||||||
chr2:241585546
|
G | A | 3 | a0001c0001t0001g0215a0002c0003t0001g0172a0002c0003t0001g0173 | 3 | HG02965.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1615-821C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585546 | ||||||
chr2:241585593
|
T | C | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1615-868A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585593 | ||||||
chr2:241585598
|
G | A | 1 | a0002c0003t0001g0242 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1615-873C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585598 | ||||||
chr2:241585625
|
C | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-900G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585625 | ||||||
chr2:241585641
|
C | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(10): Show | 13 | HG01981.hp1 HG02074.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.1615-916G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585641 | ||||||
chr2:241585647
|
G | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0222a0001c0001t0001g0226others(5): Show | 9 | HG00735.hp2 HG01081.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-922C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585647 | ||||||
chr2:241585748
|
A | G | 3 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0358 | 3 | HG02976.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1615-1023T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585748 | ||||||
chr2:241585806
|
G | A | 1 | a0002c0004t0001g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1615-1081C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585806 | ||||||
chr2:241585912
|
C | CA | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0042others(24): Show | 29 | HG00642.hp2 HG01109.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1615-1188dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(5): Show |
3 | a0001c0002t0001g0303a0001c0002t0001g0317a0001c0002t0001g0332 | 3 | HG03490.hp2 NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1615-1199_1615-118 others(16): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(6): Show |
17 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0002t0001g0276others(14): Show | 17 | HG00408.hp1 HG01993.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1615-1200_1615-118 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(7): Show |
19 | a0001c0001t0001g0145a0001c0002t0001g0026a0001c0002t0001g0281others(16): Show | 19 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-1201_1615-118 others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(8): Show |
15 | a0001c0002t0001g0197a0001c0002t0001g0282a0001c0002t0001g0285others(12): Show | 15 | HG00438.hp2 HG00639.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1615-1202_1615-118 others(19): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(9): Show |
10 | a0001c0002t0001g0025a0001c0002t0001g0283a0001c0002t0001g0284others(7): Show | 10 | HG00558.hp1 HG01952.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1615-1203_1615-118 others(20): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(10): Show |
5 | a0001c0002t0001g0105a0001c0002t0001g0286a0001c0002t0001g0334others(2): Show | 5 | HG01175.hp2 HG01891.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-1204_1615-118 others(21): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(11): Show |
4 | a0001c0002t0001g0287a0001c0002t0001g0293a0001c0002t0001g0335others(1): Show | 4 | HG00673.hp1 HG01346.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(22): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(12): Show |
5 | a0001c0002t0001g0299a0001c0002t0001g0301a0001c0002t0001g0304others(2): Show | 5 | HG00099.hp2 NA18943.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(23): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(13): Show |
3 | a0001c0002t0001g0302a0001c0002t0001g0346a0001c0002t0001g0351 | 3 | HG02080.hp1 HG03017.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(24): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(14): Show |
1 | a0002c0004t0001g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1615-1188_1615-118 others(25): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(15): Show |
2 | a0001c0002t0001g0295a0001c0002t0001g0300 | 2 | HG03831.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(26): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585912
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1615-1188_1615-118 others(30): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | ||||||
chr2:241585929
|
AG | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 7 | HG02897.hp1 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-1205delC | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585929 | ||||||
chr2:241585930
|
G | A | 129 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(126): Show | 134 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1615-1205C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585930 | ||||||
chr2:241585931
|
A | G | 1 | a0001c0002t0001g0106 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1615-1206T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585931 | ||||||
chr2:241585935
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0356 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1615-1211_1615-121 others(20): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585935 | ||||||
chr2:241585937
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1615-1212T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585937 | ||||||
chr2:241585940
|
A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0324 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1615-1216_1615-121 others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585940 | ||||||
chr2:241585994
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0358 | 3 | HG02976.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1615-1269C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585994 | ||||||
chr2:241586026
|
C | T | 1 | a0002c0003t0001g0090 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1615-1301G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586026 | ||||||
chr2:241586114
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-1389C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586114 | ||||||
chr2:241586243
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-1518G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586243 | ||||||
chr2:241586259
|
GA | G | 3 | a0001c0002t0001g0107a0002c0004t0001g0075a0002c0004t0001g0078 | 3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1615-1535delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586259 | ||||||
chr2:241586262
|
G | GA | 46 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(43): Show | 48 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1615-1538dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586262 | ||||||
chr2:241586262
|
GA | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0069others(82): Show | 97 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1615-1538delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586262 | ||||||
chr2:241586263
|
A | G | 3 | a0001c0002t0001g0107a0002c0004t0001g0075a0002c0004t0001g0078 | 3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1615-1538T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586263 | ||||||
chr2:241586363
|
G | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1615-1638C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586363 | ||||||
chr2:241586399
|
T | G | 1 | a0002c0003t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1615-1674A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586399 | ||||||
chr2:241586447
|
G | A | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-1722C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586447 | ||||||
chr2:241586581
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1615-1856G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586581 | ||||||
chr2:241586690
|
C | T | 2 | a0001c0002t0001g0330a0001c0002t0001g0338 | 2 | HG00438.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1615-1965G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586690 | ||||||
chr2:241586755
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-2030C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586755 | ||||||
chr2:241586847
|
A | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG00642.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1615-2122T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586847 | ||||||
chr2:241586874
|
C | A | 1 | a0002c0005t0001g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1615-2149G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586874 | ||||||
chr2:241586902
|
T | G | 1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-2177A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586902 | ||||||
chr2:241586917
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1615-2192T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586917 | ||||||
chr2:241587109
|
G | A | 1 | a0001c0002t0001g0333 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1615-2384C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587109 | ||||||
chr2:241587341
|
C | T | 1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-2616G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587341 | ||||||
chr2:241587499
|
T | C | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-2774A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587499 | ||||||
chr2:241587534
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-2809G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587534 | ||||||
chr2:241587582
|
G | A | 1 | a0001c0002t0001g0322 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1615-2857C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587582 | ||||||
chr2:241587665
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0234a0001c0001t0001g0236 | 4 | HG01106.hp1 HG01109.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-2940G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587665 | ||||||
chr2:241587761
|
C | T | 2 | a0001c0002t0001g0325a0001c0002t0001g0340 | 2 | NA18974.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1615-3036G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587761 | ||||||
chr2:241587764
|
A | T | 16 | a0001c0002t0001g0002a0001c0002t0001g0202a0001c0002t0001g0203others(13): Show | 18 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1615-3039T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587764 | ||||||
chr2:241587772
|
G | A | 1 | a0001c0002t0001g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1615-3047C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587772 | ||||||
chr2:241587868
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1615-3143A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587868 | ||||||
chr2:241588001
|
AAGTAAAA others(32): Show |
A | 1 | a0001c0002t0001g0352 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1615-3315_1615-327 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588001 | ||||||
chr2:241588004
|
T | A | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1615-3279A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588004 | ||||||
chr2:241588033
|
A | G | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-3308T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588033 | ||||||
chr2:241588162
|
C | T | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1615-3437G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588162 | ||||||
chr2:241588174
|
G | A | 1 | a0002c0003t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1615-3449C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588174 | ||||||
chr2:241588647
|
C | T | 1 | a0001c0002t0001g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1615-3922G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588647 | ||||||
chr2:241588711
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-3986C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588711 | ||||||
chr2:241588738
|
A | G | 1 | a0002c0003t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1615-4013T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588738 | ||||||
chr2:241589001
|
C | T | 1 | a0005c0010t0001g0035 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1615-4276G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589001 | ||||||
chr2:241589015
|
C | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-4290G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589015 | ||||||
chr2:241589015
|
C | G | 1 | a0001c0002t0001g0025 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1615-4290G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589015 | ||||||
chr2:241589076
|
G | T | 1 | a0002c0004t0003g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1615-4351C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589076 | ||||||
chr2:241589212
|
C | CA | 110 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(107): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1615-4488dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589212 | ||||||
chr2:241589212
|
C | CAA | 6 | a0001c0002t0001g0025a0001c0002t0001g0282a0001c0002t0001g0284others(3): Show | 6 | HG00639.hp1 HG01346.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615-4489_1615-448 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589212 | ||||||
chr2:241589212
|
C | CAAA | 8 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0214others(5): Show | 8 | HG01175.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-4490_1615-448 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589212 | ||||||
chr2:241589225
|
G | A | 139 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(136): Show | 144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1615-4500C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589225 | ||||||
chr2:241589366
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1615-4641C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589366 | ||||||
chr2:241589384
|
T | C | 1 | a0002c0003t0001g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1615-4659A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589384 | ||||||
chr2:241589582
|
T | G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1615-4857A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589582 | ||||||
chr2:241589664
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01516.hp1 HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1615-4939C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589664 | ||||||
chr2:241589681
|
T | C | 1 | a0003c0007t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1615-4956A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589681 | ||||||
chr2:241589695
|
G | GA | 143 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0139others(140): Show | 148 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1615-4971dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589695 | ||||||
chr2:241590012
|
T | TCAGAGCT others(32): Show |
1 | a0001c0002t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1615-5288_1615-528 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590012 | ||||||
chr2:241590012
|
TCAGAGCT others(32): Show |
T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-5326_1615-528 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590012 | ||||||
chr2:241590036
|
C | T | 139 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(136): Show | 144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1615-5311G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590036 | ||||||
chr2:241590037
|
G | A | 1 | a0002c0003t0001g0257 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1615-5312C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590037 | ||||||
chr2:241590070
|
G | A | 3 | a0001c0001t0001g0062a0001c0002t0001g0198a0001c0002t0001g0199 | 3 | HG02622.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-5345C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590070 | ||||||
chr2:241590089
|
C | T | 1 | a0002c0003t0002g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1615-5364G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590089 | ||||||
chr2:241590102
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-5377C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590102 | ||||||
chr2:241590151
|
A | G | 1 | a0001c0002t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1615-5426T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590151 | ||||||
chr2:241590332
|
C | T | 45 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(42): Show | 50 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1615-5607G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590332 | ||||||
chr2:241590339
|
A | ATGATGAG others(146): Show |
1 | a0002c0003t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1615-5615_1615-561 others(157): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590339 | ||||||
chr2:241590357
|
A | T | 1 | a0001c0001t0001g0249 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1615-5632T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590357 | ||||||
chr2:241590366
|
A | G | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5641T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590366 | ||||||
chr2:241590385
|
G | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5660C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590385 | ||||||
chr2:241590400
|
T | A | 1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5675A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590400 | ||||||
chr2:241590410
|
T | TCGGCTGA others(2018): Show |
1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5686_1615-568 others(2029): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590410 | ||||||
chr2:241590411
|
C | T | 3 | a0001c0002t0001g0107a0002c0004t0001g0075a0002c0004t0001g0078 | 3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1615-5686G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590411 | ||||||
chr2:241590422
|
A | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-5697T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590422 | ||||||
chr2:241590439
|
G | A | 1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5714C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590439 | ||||||
chr2:241590439
|
G | GCAGAGCT others(1280): Show |
1 | a0002c0004t0001g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5715_1615-571 others(1291): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590439 | ||||||
chr2:241590439
|
G | T | 1 | a0001c0001t0001g0360 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1615-5714C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590439 | ||||||
chr2:241590444
|
G | A | 1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5719C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590444 | ||||||
chr2:241590449
|
T | C | 32 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(29): Show | 36 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1615-5724A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590449 | ||||||
chr2:241590457
|
T | C | 31 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(28): Show | 35 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1615-5732A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590457 | ||||||
chr2:241590461
|
A | G | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-5736T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590461 | ||||||
chr2:241590472
|
G | T | 1 | a0001c0002t0001g0285 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1615-5747C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590472 | ||||||
chr2:241590488
|
T | C | 1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5763A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590488 | ||||||
chr2:241590496
|
T | C | 1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5771A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590496 | ||||||
chr2:241590500
|
A | G | 41 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(38): Show | 45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615-5775T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590500 | ||||||
chr2:241590517
|
A | G | 23 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0202others(20): Show | 27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5792T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590517 | ||||||
chr2:241590517
|
A | T | 1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5792T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590517 | ||||||
chr2:241590522
|
G | A | 8 | a0001c0002t0001g0200a0001c0002t0001g0201a0002c0003t0001g0176others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5797C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590522 | ||||||
chr2:241590527
|
T | C | 23 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0202others(20): Show | 27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5802A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590527 | ||||||
chr2:241590528
|
C | T | 8 | a0001c0002t0001g0200a0001c0002t0001g0201a0002c0003t0001g0176others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5803G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590528 | ||||||
chr2:241590531
|
C | CTGA | 108 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(105): Show | 109 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1615-5809_1615-580 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590531 | ||||||
chr2:241590531
|
C | CTGACGAT others(74): Show |
23 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0202others(20): Show | 27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5807_1615-580 others(85): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590531 | ||||||
chr2:241590531
|
C | CTGATGAT others(152): Show |
1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5807_1615-580 others(163): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590531 | ||||||
chr2:241590536
|
G | C | 23 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0202others(20): Show | 27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5811C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590536 | ||||||
chr2:241590536
|
G | GATC | 8 | a0001c0002t0001g0200a0001c0002t0001g0201a0002c0003t0001g0176others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5812_1615-581 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590536 | ||||||
chr2:241590538
|
T | G | 1 | a0002c0004t0001g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5813A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590538 | ||||||
chr2:241590538
|
T | TAATGGGC others(539): Show |
1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5814_1615-581 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590538 | ||||||
chr2:241590553
|
T | A | 2 | a0002c0004t0001g0171a0002c0004t0003g0159 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1615-5828A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590553 | ||||||
chr2:241590558
|
A | G | 1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5833T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590558 | ||||||
chr2:241590563
|
C | T | 1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5838G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590563 | ||||||
chr2:241590567
|
CTGA | C | 92 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1615-5845_1615-584 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590567 | ||||||
chr2:241590577
|
G | T | 1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5852C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590577 | ||||||
chr2:241590592
|
T | TCAGAACT others(305): Show |
1 | a0002c0004t0001g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5868_1615-586 others(316): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590592 | ||||||
chr2:241590602
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 8 | HG01123.hp1 HG01934.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-5877A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590602 | ||||||
chr2:241590603
|
C | T | 1 | a0002c0004t0001g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5878G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590603 | ||||||
chr2:241590610
|
T | C | 9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-5885A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590610 | ||||||
chr2:241590614
|
G | A | 31 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(28): Show | 35 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1615-5889C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590614 | ||||||
chr2:241590631
|
G | A | 1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5906C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590631 | ||||||
chr2:241590631
|
G | T | 2 | a0002c0004t0001g0171a0002c0004t0003g0159 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1615-5906C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590631 | ||||||
chr2:241590641
|
C | CCGGCTGA others(1319): Show |
1 | a0002c0003t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1615-5917_1615-591 others(1330): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590641 | ||||||
chr2:241590641
|
C | T | 2 | a0002c0004t0001g0165a0002c0004t0003g0159 | 2 | HG01123.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1615-5916G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590641 | ||||||
chr2:241590649
|
C | CGATAATG others(1550): Show |
3 | a0002c0004t0001g0157a0002c0006t0001g0155a0002c0006t0001g0156 | 3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | ||||||
chr2:241590649
|
C | CGATAATG others(1550): Show |
2 | a0001c0002t0001g0200a0001c0002t0001g0201 | 2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | ||||||
chr2:241590649
|
C | CGATAATG others(1550): Show |
1 | a0002c0004t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | ||||||
chr2:241590649
|
C | CGATAATG others(1550): Show |
1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | ||||||
chr2:241590649
|
C | T | 2 | a0002c0004t0001g0072a0002c0004t0003g0159 | 2 | HG01123.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-5924G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | ||||||
chr2:241590661
|
C | CTAGGACA others(1550): Show |
1 | a0002c0004t0001g0238 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1615-5937_1615-593 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | ||||||
chr2:241590661
|
C | CTAGGACA others(1550): Show |
7 | a0001c0002t0001g0002a0001c0002t0001g0203a0001c0002t0001g0205others(4): Show | 9 | HG00423.hp2 HG00544.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-5937_1615-593 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | ||||||
chr2:241590661
|
C | CTAGGACA others(1550): Show |
10 | a0001c0002t0001g0003a0001c0002t0001g0207a0001c0002t0001g0208others(7): Show | 12 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1615-5937_1615-593 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | ||||||
chr2:241590661
|
C | CTAGGACA others(1549): Show |
5 | a0001c0002t0001g0202a0001c0002t0001g0204a0001c0002t0001g0206others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-5937_1615-593 others(1560): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | ||||||
chr2:241590661
|
C | CTAGGACA others(305): Show |
1 | a0002c0004t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5937_1615-593 others(316): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | ||||||
chr2:241590661
|
C | G | 8 | a0001c0002t0001g0200a0001c0002t0001g0201a0002c0003t0001g0176others(5): Show | 8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5936G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | ||||||
chr2:241590682
|
G | A | 32 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(29): Show | 36 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1615-5957C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | ||||||
chr2:241590682
|
G | GGCTGATG others(539): Show |
1 | a0001c0001t0001g0136 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | ||||||
chr2:241590682
|
G | GGCTGATG others(1319): Show |
1 | a0001c0001t0001g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(1330): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | ||||||
chr2:241590682
|
G | GGCTGATG others(1709): Show |
6 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-5958_1615-595 others(1720): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | ||||||
chr2:241590682
|
G | GGCTGATG others(1709): Show |
1 | a0002c0003t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(1720): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | ||||||
chr2:241590682
|
G | GGCTGATG others(32): Show |
1 | a0002c0004t0001g0171 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | ||||||
chr2:241590720
|
T | C | 1 | a0002c0003t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1615-5995A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590720 | ||||||
chr2:241590748
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1615-6023A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590748 | ||||||
chr2:241590753
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1615-6028T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590753 | ||||||
chr2:241590797
|
T | C | 43 | a0001c0001t0001g0136a0001c0001t0001g0211a0001c0001t0001g0212others(40): Show | 47 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1615-6072A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590797 | ||||||
chr2:241590826
|
G | GCAGAGCT others(1046): Show |
1 | a0001c0002t0001g0200 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(1057): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590826
|
G | GCAGAGCT others(851): Show |
1 | a0002c0004t0003g0160 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(862): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590826
|
G | GCAGAGCT others(890): Show |
1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590826
|
G | GCAGAGCT others(890): Show |
4 | a0002c0004t0001g0157a0002c0004t0001g0161a0002c0006t0001g0155others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590826
|
G | GCAGAGCT others(890): Show |
1 | a0001c0002t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590826
|
G | GCAGAGCT others(890): Show |
24 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0201others(21): Show | 28 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590826
|
G | GCAGAGCT others(851): Show |
7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-6102_1615-610 others(862): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | ||||||
chr2:241590836
|
C | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0002t0001g0205others(1): Show | 4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6111G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590836 | ||||||
chr2:241590844
|
C | T | 42 | a0001c0001t0001g0136a0001c0001t0001g0211a0001c0001t0001g0212others(39): Show | 46 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615-6119G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590844 | ||||||
chr2:241590848
|
A | G | 39 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(36): Show | 43 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1615-6123T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590848 | ||||||
chr2:241590856
|
C | CTAGGACA others(851): Show |
1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6132_1615-613 others(862): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590856 | ||||||
chr2:241590865
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 6 | HG01934.hp2 NA18939.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615-6140T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590865 | ||||||
chr2:241590865
|
A | T | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6140T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590865 | ||||||
chr2:241590870
|
A | G | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6145T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590870 | ||||||
chr2:241590875
|
C | CCGGCTGA others(3812): Show |
1 | a0001c0002t0001g0316 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1615-6151_1615-615 others(3823): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590875 | ||||||
chr2:241590875
|
C | CCGGCTGA others(3815): Show |
1 | a0001c0002t0001g0285 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1615-6151_1615-615 others(3826): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590875 | ||||||
chr2:241590875
|
C | T | 39 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(36): Show | 43 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1615-6150G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590875 | ||||||
chr2:241590883
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6158G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590883 | ||||||
chr2:241590904
|
A | G | 1 | a0001c0002t0001g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1615-6179T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590904 | ||||||
chr2:241590904
|
A | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0236a0002c0003t0001g0176 | 3 | HG00408.hp2 HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1615-6179T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590904 | ||||||
chr2:241590909
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0236a0002c0003t0001g0176 | 3 | HG00408.hp2 HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1615-6184T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590909 | ||||||
chr2:241590914
|
C | T | 4 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0002t0001g0205others(1): Show | 4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6189G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590914 | ||||||
chr2:241590915
|
C | T | 1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-6190G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590915 | ||||||
chr2:241590922
|
C | T | 9 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(6): Show | 9 | HG00408.hp2 HG00735.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-6197G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590922 | ||||||
chr2:241590926
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0001g0236a0002c0003t0001g0176 | 3 | HG00408.hp2 HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1615-6201C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590926 | ||||||
chr2:241590943
|
A | T | 41 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(38): Show | 45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615-6218T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590943 | ||||||
chr2:241590948
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0002t0001g0205others(1): Show | 4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6223C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590948 | ||||||
chr2:241590953
|
T | C | 4 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0002t0001g0205others(1): Show | 4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6228A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0270 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 7 | HG01099.hp2 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1475): Show |
1 | a0001c0001t0001g0223 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1486): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
47 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0125others(44): Show | 52 | HG00733.hp2 HG00735.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0002g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1475): Show |
1 | a0001c0001t0001g0232 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1486): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1511): Show |
1 | a0002c0003t0001g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1522): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
35 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0040others(32): Show | 37 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(2837): Show |
2 | a0002c0003t0001g0100a0002c0003t0001g0104 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(2848): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
50 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0070others(47): Show | 55 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1512): Show |
1 | a0001c0001t0001g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1523): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1436): Show |
1 | a0001c0001t0001g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1447): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
9 | a0001c0001t0001g0008a0001c0001t0001g0063a0001c0001t0001g0065others(6): Show | 11 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(2879): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(2890): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0028 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0002g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
10 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(7): Show | 10 | HG02293.hp1 NA18953.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0032 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(14): Show | 19 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1316): Show |
1 | a0002c0003t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0247 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1553): Show |
1 | a0002c0004t0001g0076 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1564): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590953
|
T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | ||||||
chr2:241590982
|
T | A | 41 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(38): Show | 45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615-6257A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4283): Show |
1 | a0002c0004t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4294): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(1358): Show |
1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(1369): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(1589): Show |
2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(1600): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0347 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4241): Show |
1 | a0001c0002t0001g0313 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4252): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3659): Show |
7 | a0001c0002t0001g0289a0001c0002t0001g0298a0001c0002t0001g0299others(4): Show | 7 | HG00099.hp2 HG03017.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3670): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG02257.hp2 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3815): Show |
1 | a0001c0002t0001g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3826): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
2 | a0002c0004t0001g0021a0002c0004t0001g0279 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0325 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0327 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
17 | a0001c0002t0001g0314a0001c0002t0001g0317a0001c0002t0001g0318others(14): Show | 17 | HG00438.hp2 HG01928.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0322 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0025 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4205): Show |
3 | a0001c0002t0001g0310a0001c0002t0001g0311a0001c0002t0001g0312 | 3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4216): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(2099): Show |
3 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0304 | 3 | HG00558.hp1 HG00673.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(2110): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(6815): Show |
1 | a0002c0004t0001g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(6826): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
10 | a0001c0002t0001g0026a0001c0002t0001g0291a0001c0002t0001g0303others(7): Show | 10 | HG00408.hp1 NA18944.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
2 | a0001c0002t0001g0305a0001c0002t0001g0320 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
11 | a0001c0002t0001g0281a0001c0002t0001g0284a0001c0002t0001g0287others(8): Show | 11 | HG01346.hp2 HG01891.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3698): Show |
1 | a0001c0002t0001g0346 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3709): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0342 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4241): Show |
2 | a0001c0002t0001g0343a0001c0002t0001g0344 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4252): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0352 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3737): Show |
2 | a0001c0002t0001g0351a0001c0002t0001g0353 | 2 | NA18948.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3748): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3776): Show |
4 | a0001c0002t0001g0286a0001c0002t0001g0354a0001c0002t0001g0355others(1): Show | 4 | HG01175.hp2 NA18939.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(3737): Show |
1 | a0001c0002t0001g0357 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3748): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0333 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(4205): Show |
1 | a0001c0002t0001g0323 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4216): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590982
|
T | TCAGAGCT others(2528): Show |
1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(2539): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | ||||||
chr2:241590992
|
T | TTGGCTGA others(2138): Show |
1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-6268_1615-626 others(2149): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | ||||||
chr2:241590992
|
T | TTGGCTGA others(2021): Show |
1 | a0001c0001t0001g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1615-6268_1615-626 others(2032): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | ||||||
chr2:241590992
|
T | TTGGCTGA others(2177): Show |
2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-6268_1615-626 others(2188): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | ||||||
chr2:241590992
|
T | TTGGCTGA others(2021): Show |
2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-6268_1615-626 others(2032): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | ||||||
chr2:241591000
|
C | T | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6275G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591000 | ||||||
chr2:241591001
|
A | G | 177 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(174): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1615-6276T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591001 | ||||||
chr2:241591004
|
A | G | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6279T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591004 | ||||||
chr2:241591026
|
A | G | 133 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1615-6301T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591026 | ||||||
chr2:241591031
|
C | T | 133 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(130): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1615-6306G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591031 | ||||||
chr2:241591042
|
T | G | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0002c0004t0001g0075others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-6317A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591042 | ||||||
chr2:241591060
|
T | A | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6335A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591060 | ||||||
chr2:241591060
|
T | G | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-6335A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591060 | ||||||
chr2:241591074
|
CTGA | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(10): Show | 13 | HG01981.hp1 HG02074.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.1615-6352_1615-635 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591074 | ||||||
chr2:241591078
|
T | C | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6353A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591078 | ||||||
chr2:241591082
|
G | A | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6357C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591082 | ||||||
chr2:241591098
|
G | C | 142 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1615-6373C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591098 | ||||||
chr2:241591099
|
A | T | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6374T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591099 | ||||||
chr2:241591104
|
A | G | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6379T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591104 | ||||||
chr2:241591109
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6384G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591109 | ||||||
chr2:241591110
|
A | C | 142 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(139): Show | 147 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1615-6385T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591110 | ||||||
chr2:241591138
|
T | A | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6413A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591138
|
T | TCAGAGCT others(110): Show |
1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6414_1615-641 others(121): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591138
|
T | TCAGAGCT others(539): Show |
2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591138
|
T | TCAGAGCT others(500): Show |
1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-6414_1615-641 others(511): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591138
|
T | TCAGAGCT others(539): Show |
2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591138
|
T | TCAGAGCT others(539): Show |
3 | a0001c0001t0001g0062a0002c0005t0001g0153a0002c0005t0001g0154 | 3 | HG02622.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591138
|
T | TCAGAGCT others(32): Show |
132 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(129): Show | 136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | ||||||
chr2:241591148
|
C | T | 1 | a0001c0002t0001g0205 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6423G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591148 | ||||||
chr2:241591149
|
C | A | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6424G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591149 | ||||||
chr2:241591155
|
A | G | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-6430T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591155 | ||||||
chr2:241591163
|
G | C | 1 | a0001c0002t0001g0303 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1615-6438C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591163 | ||||||
chr2:241591182
|
G | A | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6457C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591182 | ||||||
chr2:241591187
|
T | C | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6462A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591187 | ||||||
chr2:241591195
|
T | C | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6470A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591195 | ||||||
chr2:241591204
|
G | A | 1 | a0001c0002t0001g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1615-6479C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591204 | ||||||
chr2:241591220
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-6495T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591220 | ||||||
chr2:241591221
|
A | G | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6496T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591221 | ||||||
chr2:241591231
|
T | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-6506A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591231 | ||||||
chr2:241591250
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1615-6525C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591250 | ||||||
chr2:241591420
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-6695G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591420 | ||||||
chr2:241591461
|
T | C | 1 | a0001c0002t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1615-6736A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591461 | ||||||
chr2:241591614
|
T | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-6889A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591614 | ||||||
chr2:241591718
|
G | A | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6993C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591718 | ||||||
chr2:241591749
|
A | T | 1 | a0002c0003t0001g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1615-7024T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591749 | ||||||
chr2:241591821
|
G | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-7096C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591821 | ||||||
chr2:241591879
|
C | G | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-7154G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591879 | ||||||
chr2:241592062
|
C | T | 2 | a0001c0002t0001g0294a0001c0002t0001g0295 | 2 | NA19006.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1615-7337G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592062 | ||||||
chr2:241592107
|
G | A | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1615-7382C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592107 | ||||||
chr2:241592184
|
G | A | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-7459C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592184 | ||||||
chr2:241592250
|
G | A | 98 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(95): Show | 98 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1615-7525C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592250 | ||||||
chr2:241592257
|
T | C | 3 | a0001c0002t0001g0310a0001c0002t0001g0311a0001c0002t0001g0312 | 3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1615-7532A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592257 | ||||||
chr2:241592333
|
C | T | 1 | a0002c0003t0001g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1615-7608G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592333 | ||||||
chr2:241592370
|
C | T | 1 | a0002c0003t0001g0172 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1615-7645G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592370 | ||||||
chr2:241592557
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1615-7832G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592557 | ||||||
chr2:241592567
|
G | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-7842C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592567 | ||||||
chr2:241592726
|
G | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18979.hp2 NA19010.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1615-8001C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592726 | ||||||
chr2:241592774
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1615-8049G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592774 | ||||||
chr2:241593014
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-8289C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593014 | ||||||
chr2:241593078
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-8353A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593078 | ||||||
chr2:241593289
|
G | A | 4 | a0002c0003t0001g0189a0002c0003t0001g0190a0002c0003t0001g0191others(1): Show | 4 | NA18945.hp2 NA18969.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-8564C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593289 | ||||||
chr2:241593337
|
C | G | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+8559G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593337 | ||||||
chr2:241593355
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+8541G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593355 | ||||||
chr2:241593373
|
T | G | 17 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1614+8523A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593373 | ||||||
chr2:241593500
|
C | A | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1614+8396G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593500 | ||||||
chr2:241593573
|
TA | T | 49 | a0001c0001t0001g0062a0001c0001t0001g0211a0001c0001t0001g0212others(46): Show | 54 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1614+8322delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593573 | ||||||
chr2:241593593
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+8303C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593593 | ||||||
chr2:241593630
|
T | G | 2 | a0001c0002t0001g0319a0001c0002t0001g0336 | 2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1614+8266A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593630 | ||||||
chr2:241593633
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+8263T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593633 | ||||||
chr2:241593635
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+8261C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593635 | ||||||
chr2:241593964
|
T | C | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1614+7932A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593964 | ||||||
chr2:241594150
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1614+7746C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594150 | ||||||
chr2:241594229
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+7667C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594229 | ||||||
chr2:241594230
|
T | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+7666A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594230 | ||||||
chr2:241594281
|
T | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+7615A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594281 | ||||||
chr2:241594615
|
G | A | 2 | a0002c0004t0001g0157a0002c0004t0001g0161 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1614+7281C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594615 | ||||||
chr2:241594721
|
G | A | 3 | a0001c0002t0001g0207a0001c0002t0001g0208a0002c0004t0001g0170 | 3 | HG00642.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1614+7175C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594721 | ||||||
chr2:241594818
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 106 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1614+7078G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594818 | ||||||
chr2:241594826
|
C | T | 3 | a0001c0002t0001g0342a0001c0002t0001g0343a0001c0002t0001g0344 | 3 | HG02559.hp1 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1614+7070G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594826 | ||||||
chr2:241594855
|
T | C | 1 | a0001c0002t0001g0316 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1614+7041A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594855 | ||||||
chr2:241594992
|
G | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+6904C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594992 | ||||||
chr2:241595003
|
T | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1614+6893A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595003 | ||||||
chr2:241595045
|
G | A | 1 | a0002c0003t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1614+6851C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595045 | ||||||
chr2:241595052
|
C | T | 131 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(128): Show | 136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1614+6844G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595052 | ||||||
chr2:241595234
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1614+6662G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595234 | ||||||
chr2:241595294
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+6602G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595294 | ||||||
chr2:241595314
|
C | T | 1 | a0002c0003t0001g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1614+6582G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595314 | ||||||
chr2:241595333
|
G | A | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1614+6563C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595333 | ||||||
chr2:241595366
|
A | G | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1614+6530T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595366 | ||||||
chr2:241595399
|
A | G | 2 | a0001c0002t0001g0292a0001c0002t0001g0293 | 2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1614+6497T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595399 | ||||||
chr2:241595412
|
C | T | 1 | a0002c0003t0002g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1614+6484G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595412 | ||||||
chr2:241595551
|
C | T | 3 | a0001c0002t0001g0200a0001c0002t0001g0201a0002c0003t0001g0093 | 3 | HG01261.hp1 HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1614+6345G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595551 | ||||||
chr2:241595594
|
G | A | 1 | a0002c0003t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614+6302C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595594 | ||||||
chr2:241595650
|
G | A | 140 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+6246C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595650 | ||||||
chr2:241595652
|
A | G | 1 | a0002c0004t0003g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1614+6244T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595652 | ||||||
chr2:241595717
|
C | G | 1 | a0002c0003t0001g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1614+6179G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595717 | ||||||
chr2:241595772
|
G | A | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+6124C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595772 | ||||||
chr2:241595783
|
C | A | 1 | a0002c0003t0001g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1614+6113G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595783 | ||||||
chr2:241595859
|
G | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0213 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+6037C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595859 | ||||||
chr2:241595922
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1614+5974A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595922 | ||||||
chr2:241595962
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+5934G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595962 | ||||||
chr2:241595970
|
G | A | 28 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(25): Show | 32 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1614+5926C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595970 | ||||||
chr2:241595990
|
A | G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1614+5906T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595990 | ||||||
chr2:241596009
|
G | A | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1614+5887C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596009 | ||||||
chr2:241596092
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+5804G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596092 | ||||||
chr2:241596148
|
A | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0210 | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+5748T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596148 | ||||||
chr2:241596163
|
A | ATT | 44 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0070others(41): Show | 49 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1614+5732_1614+573 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596163 | ||||||
chr2:241596166
|
A | T | 44 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0070others(41): Show | 49 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1614+5730T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596166 | ||||||
chr2:241596228
|
G | A | 1 | a0002c0004t0003g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1614+5668C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596228 | ||||||
chr2:241596336
|
G | A | 141 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(138): Show | 146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1614+5560C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596336 | ||||||
chr2:241596456
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1614+5440C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596456 | ||||||
chr2:241596508
|
C | CA | 22 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0038others(19): Show | 24 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1614+5387dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596508 | ||||||
chr2:241596508
|
CA | C | 92 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0144others(89): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1614+5387delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596508 | ||||||
chr2:241596508
|
CAA | C | 48 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0105others(45): Show | 48 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1614+5386_1614+538 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596508 | ||||||
chr2:241596520
|
A | G | 1 | a0002c0003t0001g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1614+5376T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596520 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1933): Show |
1 | a0001c0001t0001g0047 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1933): Show |
1 | a0001c0002t0001g0121 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1975): Show |
1 | a0001c0001t0001g0045 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1986): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1933): Show |
1 | a0001c0001t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
11 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG01981.hp1 HG02293.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1933): Show |
4 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(1): Show | 4 | HG00621.hp2 NA18941.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(13): Show | 18 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1931): Show |
1 | a0001c0001t0001g0056 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1931): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0234a0001c0001t0001g0236 | 4 | HG01106.hp1 HG01109.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1933): Show |
9 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
104 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0014others(101): Show | 115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
1 | a0001c0002t0001g0124 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
1 | a0006c0008t0001g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
3 | a0001c0002t0001g0107a0002c0004t0001g0075a0002c0004t0001g0078 | 3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
1 | a0002c0003t0001g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
7 | a0001c0002t0001g0310a0001c0002t0001g0311a0001c0002t0001g0312others(4): Show | 7 | HG00438.hp2 HG01891.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1931): Show |
113 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(110): Show | 118 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1930): Show |
3 | a0001c0002t0001g0289a0001c0002t0001g0308a0001c0002t0001g0327 | 3 | HG03491.hp2 NA18942.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1931): Show |
1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1933): Show |
1 | a0002c0004t0003g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1927): Show |
1 | a0002c0004t0003g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1938): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1931): Show |
3 | a0002c0004t0003g0158a0002c0004t0003g0159a0002c0004t0003g0160 | 3 | HG01081.hp1 HG01123.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1931): Show |
1 | a0001c0002t0001g0335 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1930): Show |
1 | a0002c0004t0001g0167 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1932): Show |
1 | a0001c0001t0001g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1930): Show |
7 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596529
|
G | GGGCGCGG others(1930): Show |
1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | ||||||
chr2:241596531
|
G | GCGCGGTG others(1931): Show |
1 | a0001c0002t0001g0286 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1614+5364_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596531 | ||||||
chr2:241596537
|
T | C | 1 | a0001c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1614+5359A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596537 | ||||||
chr2:241596579
|
C | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1614+5317G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596579 | ||||||
chr2:241596623
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1614+5273C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596623 | ||||||
chr2:241596653
|
G | T | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+5243C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596653 | ||||||
chr2:241596759
|
C | T | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+5137G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596759 | ||||||
chr2:241596801
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0246a0001c0001t0001g0249others(2): Show | 7 | HG00558.hp2 NA18612.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1614+5095C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596801 | ||||||
chr2:241596892
|
G | C | 1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1614+5004C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596892 | ||||||
chr2:241597027
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1614+4869G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597027 | ||||||
chr2:241597170
|
G | A | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+4726C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597170 | ||||||
chr2:241597236
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1614+4660G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597236 | ||||||
chr2:241597426
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0002c0003t0001g0103 | 3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1614+4470C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597426 | ||||||
chr2:241597483
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1614+4413T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597483 | ||||||
chr2:241597533
|
C | T | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+4363G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597533 | ||||||
chr2:241597568
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1614+4328A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597568 | ||||||
chr2:241597717
|
G | A | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+4179C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597717 | ||||||
chr2:241597926
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+3970C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597926 | ||||||
chr2:241597978
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1614+3918G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597978 | ||||||
chr2:241597978
|
CA | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1614+3917delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597978 | ||||||
chr2:241597978
|
CAA | C | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 141 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1614+3916_1614+391 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597978 | ||||||
chr2:241598004
|
A | G | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+3892T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598004 | ||||||
chr2:241598007
|
A | T | 1 | a0001c0002t0001g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1614+3889T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598007 | ||||||
chr2:241598277
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+3619G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598277 | ||||||
chr2:241598291
|
G | A | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+3605C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598291 | ||||||
chr2:241598415
|
TC | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+3480delG | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598415 | ||||||
chr2:241598421
|
A | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 5 | HG00597.hp2 HG00621.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+3475T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598421 | ||||||
chr2:241598453
|
T | G | 1 | a0001c0002t0001g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1614+3443A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598453 | ||||||
chr2:241598518
|
A | AT | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0002c0003t0001g0263 | 3 | HG01099.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1614+3377dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598518 | ||||||
chr2:241598647
|
T | G | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+3249A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598647 | ||||||
chr2:241598735
|
C | T | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1614+3161G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598735 | ||||||
chr2:241598860
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1614+3036A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598860 | ||||||
chr2:241598875
|
C | G | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1614+3021G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598875 | ||||||
chr2:241598876
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1614+3020A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598876 | ||||||
chr2:241598907
|
G | A | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+2989C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598907 | ||||||
chr2:241598912
|
G | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(3): Show | 6 | HG00735.hp1 HG01123.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+2984C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598912 | ||||||
chr2:241598924
|
GA | G | 139 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(136): Show | 144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1614+2971delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598924 | ||||||
chr2:241599060
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0129 | 4 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+2836A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599060 | ||||||
chr2:241599081
|
A | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1614+2815T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599081 | ||||||
chr2:241599129
|
G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+2767C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599129 | ||||||
chr2:241599183
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+2713G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599183 | ||||||
chr2:241599206
|
C | T | 4 | a0001c0002t0001g0314a0001c0002t0001g0317a0001c0002t0001g0318others(1): Show | 4 | HG03490.hp2 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+2690G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599206 | ||||||
chr2:241599251
|
C | CA | 108 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(105): Show | 109 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1614+2644dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599251 | ||||||
chr2:241599251
|
C | CAA | 36 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(33): Show | 40 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1614+2643_1614+264 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599251 | ||||||
chr2:241599521
|
C | T | 57 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0069others(54): Show | 63 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1614+2375G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599521 | ||||||
chr2:241599528
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1614+2368T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599528 | ||||||
chr2:241599532
|
A | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0210 | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+2364T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599532 | ||||||
chr2:241599567
|
C | G | 1 | a0001c0002t0001g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1614+2329G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599567 | ||||||
chr2:241599711
|
C | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+2185G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599711 | ||||||
chr2:241599828
|
G | C | 2 | a0002c0006t0001g0155a0002c0006t0001g0156 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1614+2068C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599828 | ||||||
chr2:241599831
|
A | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+2065T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599831 | ||||||
chr2:241599911
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1614+1985G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599911 | ||||||
chr2:241599930
|
C | T | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1614+1966G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599930 | ||||||
chr2:241599957
|
C | G | 1 | a0001c0002t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1614+1939G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599957 | ||||||
chr2:241599965
|
T | G | 1 | a0002c0003t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1614+1931A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599965 | ||||||
chr2:241600089
|
G | A | 1 | a0001c0002t0001g0313 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1614+1807C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600089 | ||||||
chr2:241600095
|
C | T | 1 | a0001c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1614+1801G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600095 | ||||||
chr2:241600133
|
C | T | 1 | a0001c0002t0001g0322 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1614+1763G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600133 | ||||||
chr2:241600245
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+1651A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600245 | ||||||
chr2:241600249
|
C | G | 302 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1614+1647G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600249 | ||||||
chr2:241600316
|
T | C | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+1580A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600316 | ||||||
chr2:241600531
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0213 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+1365A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600531 | ||||||
chr2:241600555
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+1341C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600555 | ||||||
chr2:241600727
|
C | CA | 89 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0128others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1614+1168dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600727 | ||||||
chr2:241600727
|
C | CAA | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(39): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1614+1167_1614+116 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600727 | ||||||
chr2:241600727
|
C | CAAA | 46 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0211others(43): Show | 53 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1614+1166_1614+116 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600727 | ||||||
chr2:241600975
|
TA | T | 139 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144others(136): Show | 143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1614+920delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600975 | ||||||
chr2:241600976
|
A | T | 1 | a0002c0003t0001g0259 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1614+920T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600976 | ||||||
chr2:241601063
|
G | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 8 | HG01934.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1614+833C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601063 | ||||||
chr2:241601096
|
T | C | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+800A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601096 | ||||||
chr2:241601138
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1614+758G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601138 | ||||||
chr2:241601147
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1614+749C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601147 | ||||||
chr2:241601222
|
G | A | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+674C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601222 | ||||||
chr2:241601226
|
C | T | 92 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1614+670G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601226 | ||||||
chr2:241601264
|
C | A | 1 | a0001c0002t0001g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1614+632G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601264 | ||||||
chr2:241601323
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1614+573T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601323 | ||||||
chr2:241601435
|
G | A | 1 | a0001c0002t0001g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1614+461C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601435 | ||||||
chr2:241601632
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1614+264C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601632 | ||||||
chr2:241601820
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1614+76C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601820 | ||||||
chr2:241601839
|
T | C | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+57A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601839 | ||||||
chr2:241601874
|
C | T | 1 | a0002c0004t0003g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1614+22G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601874 | ||||||
chr2:241602038
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1511-39G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602038 | ||||||
chr2:241602058
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1511-59A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602058 | ||||||
chr2:241602197
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1511-198C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602197 | ||||||
chr2:241602350
|
G | A | 67 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(64): Show | 73 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1511-351C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602350 | ||||||
chr2:241602358
|
G | GT | 17 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0055others(14): Show | 17 | HG00438.hp2 HG00544.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.1511-360dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602358 | ||||||
chr2:241602372
|
C | CA | 3 | a0001c0001t0001g0132a0001c0001t0001g0230a0002c0003t0001g0183 | 3 | HG00733.hp2 HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1511-374_1511-373i others(3): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602372 | ||||||
chr2:241602554
|
C | T | 1 | a0002c0003t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510+416G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602554 | ||||||
chr2:241602804
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1510+166C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602804 | ||||||
chr2:241602883
|
T | C | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1510+87A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602883 | ||||||
chr2:241602889
|
T | C | 7 | a0001c0002t0001g0002a0001c0002t0001g0203a0001c0002t0001g0205others(4): Show | 9 | HG00423.hp2 HG00544.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1510+81A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602889 | ||||||
chr2:241603084
|
A | T | 1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | splice_region_variant&intron_variant | LOW | c.1401-5T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603084 | ||||||
chr2:241603139
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1401-60G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603139 | ||||||
chr2:241603259
|
T | C | 3 | a0001c0002t0001g0305a0001c0002t0001g0320a0002c0004t0001g0277 | 3 | HG03654.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1401-180A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603259 | ||||||
chr2:241603294
|
ACACACCT others(193): Show |
A | 42 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0040others(39): Show | 44 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1401-415_1401-216d others(2): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603294 | ||||||
chr2:241603311
|
C | T | 2 | a0002c0004t0001g0075a0002c0004t0001g0078 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1401-232G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603311 | ||||||
chr2:241603380
|
T | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1401-301A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603380 | ||||||
chr2:241603394
|
G | A | 130 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(127): Show | 134 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1401-315C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603394 | ||||||
chr2:241603588
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1401-509A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603588 | ||||||
chr2:241603775
|
C | G | 2 | a0001c0002t0001g0322a0001c0002t0001g0323 | 2 | NA18982.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1401-696G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603775 | ||||||
chr2:241603883
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401-804A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603883 | ||||||
chr2:241603958
|
GCTGGGCA others(9): Show |
G | 1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1401-895_1401-880d others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603958 | ||||||
chr2:241604222
|
C | T | 2 | a0002c0003t0001g0185a0002c0003t0001g0196 | 2 | HG02895.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1401-1143G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604222 | ||||||
chr2:241604236
|
A | AATTT | 20 | a0001c0001t0001g0062a0001c0001t0001g0268a0001c0001t0001g0269others(17): Show | 21 | HG02056.hp2 HG02523.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1401-1161_1401-115 others(8): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604236 | ||||||
chr2:241604375
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1401-1296G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604375 | ||||||
chr2:241604644
|
TAGTGATC others(141): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1400+1522_1401-156 others(4): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604644 | ||||||
chr2:241604807
|
C | G | 1 | a0001c0002t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1400+1507G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604807 | ||||||
chr2:241605182
|
C | T | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1400+1132G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605182 | ||||||
chr2:241605326
|
C | T | 1 | a0002c0003t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1400+988G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605326 | ||||||
chr2:241605330
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1400+984C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605330 | ||||||
chr2:241605339
|
A | G | 3 | a0002c0003t0001g0091a0002c0003t0001g0094a0002c0003t0001g0099 | 3 | HG00741.hp2 HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1400+975T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605339 | ||||||
chr2:241605452
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1400+862A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605452 | ||||||
chr2:241605510
|
A | G | 35 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(32): Show | 40 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1400+804T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605510 | ||||||
chr2:241605547
|
A | T | 176 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1400+767T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605547 | ||||||
chr2:241605718
|
T | A | 1 | a0002c0003t0001g0093 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1400+596A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605718 | ||||||
chr2:241605722
|
C | CT | 42 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0070others(39): Show | 47 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1400+591dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605722 | ||||||
chr2:241605982
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1400+332C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605982 | ||||||
chr2:241606036
|
A | C | 1 | a0001c0001t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1400+278T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606036 | ||||||
chr2:241606191
|
T | G | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+123A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606191 | ||||||
chr2:241606192
|
A | C | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+122T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606192 | ||||||
chr2:241606193
|
G | A | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+121C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606193 | ||||||
chr2:241606199
|
C | A | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+115G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606199 | ||||||
chr2:241606202
|
G | C | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+112C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606202 | ||||||
chr2:241606204
|
T | C | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+110A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606204 | ||||||
chr2:241606205
|
C | A | 1 | a0001c0002t0004g0362 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+109G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606205 | ||||||
chr2:241606241
|
C | A | 1 | a0001c0002t0001g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1400+73G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606241 | ||||||
chr2:241606301
|
G | A | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1400+13C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606301 | ||||||
chr2:241606894
|
C | A | 41 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(38): Show | 45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1241-421G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606894 | ||||||
chr2:241606928
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-455G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606928 | ||||||
chr2:241606948
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-475G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606948 | ||||||
chr2:241606980
|
CA | C | 15 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(12): Show | 15 | HG02056.hp2 HG02523.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1241-508delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606980 | ||||||
chr2:241607007
|
G | C | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-534C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607007 | ||||||
chr2:241607063
|
T | A | 1 | a0001c0002t0001g0200 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1241-590A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607063 | ||||||
chr2:241607372
|
G | A | 1 | a0001c0002t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1241-899C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607372 | ||||||
chr2:241607411
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1241-938C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607411 | ||||||
chr2:241607467
|
G | A | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1241-994C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607467 | ||||||
chr2:241607471
|
G | T | 1 | a0001c0002t0001g0319 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1241-998C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607471 | ||||||
chr2:241607519
|
C | T | 37 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(34): Show | 37 | HG00438.hp2 HG01928.hp2 HG01993.hp2 others(34): Show |
intron_variant | MODIFIER | c.1241-1046G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607519 | ||||||
chr2:241607597
|
C | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(32): Show | 37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-1124G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607597 | ||||||
chr2:241607645
|
C | T | 1 | a0001c0002t0001g0338 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1241-1172G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607645 | ||||||
chr2:241607672
|
G | C | 1 | a0001c0002t0001g0310 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1241-1199C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607672 | ||||||
chr2:241607673
|
C | G | 1 | a0001c0002t0001g0310 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1241-1200G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607673 | ||||||
chr2:241607685
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241-1212C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607685 | ||||||
chr2:241607689
|
G | A | 35 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(32): Show | 40 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-1216C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607689 | ||||||
chr2:241607691
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1241-1218C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607691 | ||||||
chr2:241607718
|
A | G | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1241-1245T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607718 | ||||||
chr2:241607733
|
C | CCCCAGTG others(58): Show |
2 | a0001c0001t0001g0132a0002c0003t0001g0088 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1241-1325_1241-126 others(69): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607733 | ||||||
chr2:241607887
|
G | A | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1241-1414C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607887 | ||||||
chr2:241607900
|
A | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1241-1427T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607900 | ||||||
chr2:241607906
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-1433G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607906 | ||||||
chr2:241607934
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-1461G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607934 | ||||||
chr2:241607960
|
A | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-1487T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607960 | ||||||
chr2:241608127
|
G | T | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-1654C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608127 | ||||||
chr2:241608150
|
T | C | 1 | a0002c0004t0001g0076 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1241-1677A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608150 | ||||||
chr2:241608212
|
T | G | 1 | a0001c0002t0004g0363 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1241-1739A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608212 | ||||||
chr2:241608251
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-1778C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608251 | ||||||
chr2:241608389
|
T | C | 1 | a0001c0002t0001g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1241-1916A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608389 | ||||||
chr2:241608409
|
A | G | 3 | a0001c0002t0001g0205a0001c0002t0001g0341a0002c0004t0001g0168 | 3 | HG02132.hp1 NA19000.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1241-1936T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608409 | ||||||
chr2:241608549
|
C | T | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(31): Show | 36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1241-2076G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608549 | ||||||
chr2:241608620
|
T | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-2147A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608620 | ||||||
chr2:241608690
|
C | T | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-2217G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608690 | ||||||
chr2:241608802
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-2329C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608802 | ||||||
chr2:241608977
|
G | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA19070.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1241-2504C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608977 | ||||||
chr2:241609293
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-2820C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609293 | ||||||
chr2:241609343
|
G | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-2870C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609343 | ||||||
chr2:241609425
|
A | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | NA18960.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1241-2952T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609425 | ||||||
chr2:241609443
|
G | A | 3 | a0001c0002t0001g0207a0001c0002t0001g0208a0002c0004t0001g0170 | 3 | HG00642.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1241-2970C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609443 | ||||||
chr2:241609483
|
T | C | 35 | a0001c0001t0001g0211a0001c0001t0001g0213a0001c0002t0001g0002others(32): Show | 39 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1241-3010A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609483 | ||||||
chr2:241609543
|
T | C | 1 | a0002c0003t0001g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1241-3070A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609543 | ||||||
chr2:241609652
|
T | C | 1 | a0001c0002t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1241-3179A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609652 | ||||||
chr2:241609718
|
C | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-3245G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609718 | ||||||
chr2:241609718
|
C | T | 1 | a0001c0002t0001g0019 | 2 | NA18971.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1241-3245G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609718 | ||||||
chr2:241609772
|
G | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-3299C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609772 | ||||||
chr2:241609782
|
C | CA | 134 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1241-3310dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609782 | ||||||
chr2:241610045
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1241-3572C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610045 | ||||||
chr2:241610068
|
G | T | 1 | a0001c0002t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1241-3595C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610068 | ||||||
chr2:241610139
|
A | G | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1241-3666T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610139 | ||||||
chr2:241610197
|
C | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0058 | 2 | NA18949.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1241-3724G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610197 | ||||||
chr2:241610209
|
A | G | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1241-3736T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610209 | ||||||
chr2:241610287
|
A | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1241-3814T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610287 | ||||||
chr2:241610317
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0213 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1241-3844G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610317 | ||||||
chr2:241610327
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-3854A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610327 | ||||||
chr2:241610515
|
G | C | 1 | a0002c0003t0001g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1241-4042C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610515 | ||||||
chr2:241610532
|
A | G | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1241-4059T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610532 | ||||||
chr2:241610534
|
C | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-4061G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610534 | ||||||
chr2:241610553
|
G | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0203 | 4 | HG00423.hp2 HG02135.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-4080C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610553 | ||||||
chr2:241610620
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1241-4147G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610620 | ||||||
chr2:241610640
|
C | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-4167G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610640 | ||||||
chr2:241610784
|
A | C | 2 | a0002c0003t0001g0100a0002c0003t0001g0104 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1241-4311T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610784 | ||||||
chr2:241610869
|
TGGGGCCA others(5): Show |
T | 3 | a0001c0001t0001g0275a0002c0003t0001g0196a0002c0003t0001g0261 | 3 | HG02895.hp2 HG03491.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1241-4408_1241-439 others(16): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610869 | ||||||
chr2:241610891
|
G | A | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1241-4418C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610891 | ||||||
chr2:241610995
|
C | A | 12 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0239others(9): Show | 13 | HG01071.hp2 HG01168.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-4522G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610995 | ||||||
chr2:241611120
|
T | G | 90 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(87): Show | 90 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1241-4647A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611120 | ||||||
chr2:241611316
|
GC | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0234a0001c0001t0001g0236 | 4 | HG01106.hp1 HG01109.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-4844delG | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611316 | ||||||
chr2:241611399
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1241-4926T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611399 | ||||||
chr2:241611724
|
C | CA | 8 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0045others(5): Show | 9 | HG01106.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-5252dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611724 | ||||||
chr2:241611724
|
CA | C | 134 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(131): Show | 138 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1241-5252delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611724 | ||||||
chr2:241611955
|
T | C | 91 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-5482A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611955 | ||||||
chr2:241611959
|
G | A | 91 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-5486C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611959 | ||||||
chr2:241611971
|
C | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-5498G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611971 | ||||||
chr2:241612097
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-5624G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612097 | ||||||
chr2:241612117
|
G | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-5644C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612117 | ||||||
chr2:241612124
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-5651T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612124 | ||||||
chr2:241612220
|
G | A | 1 | a0002c0004t0001g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1241-5747C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612220 | ||||||
chr2:241612243
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1241-5770C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612243 | ||||||
chr2:241612279
|
G | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0002c0003t0001g0103 | 3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1241-5806C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612279 | ||||||
chr2:241612304
|
G | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-5831C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612304 | ||||||
chr2:241612309
|
C | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-5836G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612309 | ||||||
chr2:241612329
|
G | T | 1 | a0001c0002t0001g0112 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1241-5856C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612329 | ||||||
chr2:241612429
|
C | T | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-5956G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612429 | ||||||
chr2:241612430
|
T | A | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-5957A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612430 | ||||||
chr2:241612464
|
C | T | 1 | a0001c0002t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1241-5991G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612464 | ||||||
chr2:241612912
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1241-6439G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612912 | ||||||
chr2:241612932
|
C | G | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-6459G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612932 | ||||||
chr2:241612964
|
T | C | 91 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-6491A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612964 | ||||||
chr2:241613274
|
C | CA | 9 | a0001c0001t0001g0042a0001c0001t0001g0139a0001c0001t0001g0229others(6): Show | 9 | HG01891.hp1 HG02148.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.1241-6802dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613274 | ||||||
chr2:241613274
|
CA | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0211others(3): Show | 6 | HG02080.hp2 HG02897.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-6802delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613274 | ||||||
chr2:241613289
|
A | G | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-6816T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613289 | ||||||
chr2:241613306
|
C | CA | 5 | a0001c0002t0001g0324a0001c0002t0001g0325a0001c0002t0001g0326others(2): Show | 5 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-6834dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613306 | ||||||
chr2:241613412
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0066others(1): Show | 5 | HG02145.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-6939T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613412 | ||||||
chr2:241613635
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1241-7162C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613635 | ||||||
chr2:241613659
|
G | C | 2 | a0001c0002t0001g0200a0001c0002t0001g0201 | 2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1241-7186C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613659 | ||||||
chr2:241613775
|
A | G | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0002c0004t0001g0075others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-7302T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613775 | ||||||
chr2:241614407
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-7934G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614407 | ||||||
chr2:241614801
|
A | G | 1 | a0001c0002t0001g0356 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1241-8328T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614801 | ||||||
chr2:241614889
|
CAAAACA | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0271a0002c0003t0001g0020others(1): Show | 5 | HG02559.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-8422_1241-841 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614889 | ||||||
chr2:241614889
|
CAAAACAA others(5): Show |
C | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-8428_1241-841 others(16): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614889 | ||||||
chr2:241615065
|
A | G | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1241-8592T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615065 | ||||||
chr2:241615071
|
T | C | 1 | a0002c0004t0001g0168 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1241-8598A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615071 | ||||||
chr2:241615091
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1241-8618G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615091 | ||||||
chr2:241615101
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1241-8628C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615101 | ||||||
chr2:241615159
|
G | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-8686C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615159 | ||||||
chr2:241615244
|
G | A | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-8771C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615244 | ||||||
chr2:241615288
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-8815G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615288 | ||||||
chr2:241615362
|
C | A | 1 | a0001c0002t0001g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1241-8889G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615362 | ||||||
chr2:241615411
|
C | A | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1241-8938G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615411 | ||||||
chr2:241615497
|
C | T | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-9024G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615497 | ||||||
chr2:241615665
|
G | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-9192C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615665 | ||||||
chr2:241615727
|
G | A | 1 | a0001c0002t0001g0152 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1241-9254C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615727 | ||||||
chr2:241615797
|
C | T | 1 | a0002c0003t0001g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1241-9324G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615797 | ||||||
chr2:241615834
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1241-9361T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615834 | ||||||
chr2:241615841
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0210 | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-9368C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615841 | ||||||
chr2:241615848
|
G | A | 1 | a0002c0003t0001g0090 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1241-9375C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615848 | ||||||
chr2:241615869
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1241-9396C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615869 | ||||||
chr2:241615881
|
C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0002t0001g0351others(5): Show | 8 | HG02074.hp1 NA18939.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241-9408G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615881 | ||||||
chr2:241615901
|
G | A | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-9428C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615901 | ||||||
chr2:241615987
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1241-9514T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615987 | ||||||
chr2:241615993
|
C | T | 4 | a0002c0003t0001g0082a0002c0003t0001g0083a0002c0003t0001g0090others(1): Show | 4 | HG00733.hp1 HG01993.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-9520G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615993 | ||||||
chr2:241616038
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-9565C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616038 | ||||||
chr2:241616165
|
T | C | 2 | a0002c0004t0001g0021a0002c0004t0001g0279 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1241-9692A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616165 | ||||||
chr2:241616182
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1241-9709G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616182 | ||||||
chr2:241616183
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1241-9710C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616183 | ||||||
chr2:241616281
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241-9808T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616281 | ||||||
chr2:241616654
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1241-10181T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616654 | ||||||
chr2:241616722
|
T | A | 1 | a0002c0003t0001g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1241-10249A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616722 | ||||||
chr2:241616746
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1241-10273G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616746 | ||||||
chr2:241616882
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-10409C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616882 | ||||||
chr2:241616926
|
A | G | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1241-10453T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616926 | ||||||
chr2:241616991
|
C | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-10518G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616991 | ||||||
chr2:241617000
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0234a0001c0001t0001g0236 | 4 | HG01106.hp1 HG01109.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-10527G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617000 | ||||||
chr2:241617114
|
A | G | 5 | a0001c0002t0001g0026a0001c0002t0001g0352a0001c0002t0004g0362others(2): Show | 5 | NA18974.hp1 NA18981.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-10641T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617114 | ||||||
chr2:241617119
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1241-10646A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617119 | ||||||
chr2:241617280
|
C | G | 3 | a0002c0004t0003g0158a0002c0004t0003g0159a0002c0004t0003g0160 | 3 | HG01081.hp1 HG01123.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1241-10807G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617280 | ||||||
chr2:241617317
|
G | A | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-10844C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617317 | ||||||
chr2:241617435
|
C | T | 1 | a0001c0002t0001g0355 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1241-10962G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617435 | ||||||
chr2:241617592
|
G | C | 1 | a0001c0002t0001g0335 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1241-11119C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617592 | ||||||
chr2:241617604
|
G | A | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-11131C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617604 | ||||||
chr2:241617613
|
G | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-11140C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617613 | ||||||
chr2:241617717
|
C | T | 1 | a0001c0002t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1241-11244G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617717 | ||||||
chr2:241617764
|
A | C | 136 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(133): Show | 140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-11291T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617764 | ||||||
chr2:241617782
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1241-11309G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617782 | ||||||
chr2:241617936
|
A | T | 1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1241-11463T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617936 | ||||||
chr2:241618015
|
T | G | 326 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(323): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1241-11542A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618015 | ||||||
chr2:241618101
|
C | T | 1 | a0002c0004t0003g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1241-11628G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618101 | ||||||
chr2:241618139
|
C | T | 91 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-11666G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618139 | ||||||
chr2:241618147
|
T | C | 1 | a0002c0003t0001g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1241-11674A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618147 | ||||||
chr2:241618231
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-11758G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618231 | ||||||
chr2:241618232
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 6 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-11759C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618232 | ||||||
chr2:241618344
|
T | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-11871A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618344 | ||||||
chr2:241618370
|
T | C | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1241-11897A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618370 | ||||||
chr2:241618512
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1241-12039C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618512 | ||||||
chr2:241618540
|
G | C | 1 | a0002c0004t0001g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1241-12067C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618540 | ||||||
chr2:241618603
|
A | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-12130T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618603 | ||||||
chr2:241618662
|
C | T | 1 | a0001c0002t0001g0329 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1241-12189G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618662 | ||||||
chr2:241619168
|
C | T | 1 | a0001c0002t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1241-12695G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619168 | ||||||
chr2:241619172
|
G | A | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1241-12699C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619172 | ||||||
chr2:241619267
|
G | C | 1 | a0001c0002t0001g0335 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1241-12794C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619267 | ||||||
chr2:241619362
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-12889G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619362 | ||||||
chr2:241619441
|
G | A | 1 | a0002c0003t0001g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1241-12968C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619441 | ||||||
chr2:241619499
|
T | C | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(6): Show | 9 | HG02056.hp2 HG02523.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-13026A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619499 | ||||||
chr2:241619698
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+13219A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619698 | ||||||
chr2:241619726
|
C | CGGTGAGG others(4): Show |
1 | a0001c0002t0001g0012 | 2 | NA18943.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1240+13180_1240+13 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619726 | ||||||
chr2:241619756
|
T | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1240+13161A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619756 | ||||||
chr2:241619782
|
T | C | 2 | a0001c0001t0001g0141a0002c0003t0001g0081 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+13135A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619782 | ||||||
chr2:241619796
|
G | T | 2 | a0001c0001t0001g0141a0002c0003t0001g0081 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+13121C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619796 | ||||||
chr2:241619831
|
CGTGAGTG others(4): Show |
C | 94 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(91): Show | 94 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1240+13075_1240+13 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619831 | ||||||
chr2:241619842
|
G | GGTGAGTG others(37): Show |
1 | a0001c0002t0001g0281 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1240+13074_1240+13 others(50): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619842 | ||||||
chr2:241619863
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0246a0001c0001t0001g0247others(14): Show | 19 | HG00558.hp2 HG00621.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240+13054C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619863 | ||||||
chr2:241619867
|
CGGTGAGT others(4): Show |
C | 50 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0043others(47): Show | 56 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1240+13039_1240+13 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619867 | ||||||
chr2:241619938
|
G | C | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1240+12979C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619938 | ||||||
chr2:241619978
|
CGGTGAGT others(4): Show |
C | 1 | a0001c0002t0001g0200 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1240+12928_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619978 | ||||||
chr2:241619980
|
GTGAGTGA others(27): Show |
G | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+12903_1240+12 others(40): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619980 | ||||||
chr2:241619990
|
GGTGA | G | 96 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(93): Show | 96 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1240+12923_1240+12 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619990 | ||||||
chr2:241620001
|
C | T | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12916G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620001 | ||||||
chr2:241620002
|
A | G | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12915T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620002 | ||||||
chr2:241620013
|
G | A | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12904C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620013 | ||||||
chr2:241620014
|
A | G | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12903T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620014 | ||||||
chr2:241620023
|
GGGTGAGT others(1): Show |
G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+12886_1240+12 others(14): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620023 | ||||||
chr2:241620031
|
T | G | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+12886A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620031 | ||||||
chr2:241620032
|
G | GGTGAGTG others(4): Show |
9 | a0001c0001t0001g0216a0002c0003t0001g0097a0002c0003t0001g0187others(6): Show | 9 | HG00544.hp2 HG00597.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+12874_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620032 | ||||||
chr2:241620042
|
G | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+12875C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620042 | ||||||
chr2:241620043
|
A | AGTGAGTG others(4): Show |
3 | a0001c0002t0001g0204a0002c0004t0001g0009a0002c0004t0001g0072 | 4 | HG02818.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+12863_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620043 | ||||||
chr2:241620043
|
A | C | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+12874T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620043 | ||||||
chr2:241620043
|
A | G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+12874T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620043 | ||||||
chr2:241620053
|
G | C | 1 | a0001c0002t0001g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1240+12864C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620053 | ||||||
chr2:241620063
|
G | GT | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12853_1240+12 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620063 | ||||||
chr2:241620064
|
G | C | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12853C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620064 | ||||||
chr2:241620074
|
GTCGT | G | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12839_1240+12 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620074 | ||||||
chr2:241620080
|
A | G | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12837T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620080 | ||||||
chr2:241620090
|
G | A | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12827C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620090 | ||||||
chr2:241620175
|
GTGAGTCG others(20): Show |
G | 1 | a0001c0001t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1240+12715_1240+12 others(33): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620175 | ||||||
chr2:241620182
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+12735C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620182 | ||||||
chr2:241620193
|
G | GGTGAGGA others(4): Show |
140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+12713_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620193 | ||||||
chr2:241620195
|
TGAG | T | 3 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | NA18962.hp2 NA18984.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1240+12719_1240+12 others(9): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620195 | ||||||
chr2:241620198
|
GGAGT | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(31): Show | 36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1240+12715_1240+12 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620198 | ||||||
chr2:241620206
|
TGAG | T | 3 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | NA18962.hp2 NA18984.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1240+12708_1240+12 others(9): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620206 | ||||||
chr2:241620210
|
G | C | 3 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | NA18962.hp2 NA18984.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1240+12707C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620210 | ||||||
chr2:241620234
|
GGTGAGGA others(4): Show |
G | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+12672_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620234 | ||||||
chr2:241620270
|
GGTGAGTG others(4): Show |
G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+12636_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620270 | ||||||
chr2:241620281
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1240+12636G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620281 | ||||||
chr2:241620304
|
G | A | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+12613C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620304 | ||||||
chr2:241620326
|
GGTGAGTG others(5): Show |
G | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+12579_1240+12 others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620326 | ||||||
chr2:241620365
|
AGTGAGGG | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+12545_1240+12 others(13): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620365 | ||||||
chr2:241620380
|
G | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+12537C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620380 | ||||||
chr2:241620425
|
G | C | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+12492C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620425 | ||||||
chr2:241620477
|
T | TGGTGAGT others(15): Show |
1 | a0002c0003t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+12418_1240+12 others(28): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620477 | ||||||
chr2:241620477
|
TGGTGAGT others(4): Show |
T | 1 | a0001c0001t0001g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1240+12429_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620477 | ||||||
chr2:241620489
|
A | AGTGAGTG others(4): Show |
4 | a0001c0002t0001g0354a0001c0002t0001g0355a0001c0002t0001g0356others(1): Show | 4 | NA18939.hp2 NA18953.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+12417_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620489 | ||||||
chr2:241620512
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038 | 3 | HG00438.hp1 HG00673.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1240+12405C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620512 | ||||||
chr2:241620533
|
C | T | 1 | a0002c0003t0001g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1240+12384G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620533 | ||||||
chr2:241620533
|
CGGTGACT others(4): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1240+12373_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620533 | ||||||
chr2:241620614
|
A | ATGAGTGA others(27): Show |
1 | a0002c0003t0001g0089 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1240+12269_1240+12 others(40): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620614 | ||||||
chr2:241620728
|
G | A | 1 | a0001c0002t0001g0336 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+12189C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620728 | ||||||
chr2:241620729
|
A | C | 1 | a0001c0002t0001g0336 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+12188T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620729 | ||||||
chr2:241620742
|
T | C | 1 | a0002c0003t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1240+12175A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620742 | ||||||
chr2:241620826
|
C | T | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1240+12091G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620826 | ||||||
chr2:241620877
|
T | C | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12040A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620877 | ||||||
chr2:241620926
|
T | C | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+11991A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620926 | ||||||
chr2:241621252
|
G | A | 1 | a0001c0002t0001g0116 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1240+11665C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621252 | ||||||
chr2:241621402
|
T | C | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1240+11515A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621402 | ||||||
chr2:241621471
|
G | C | 1 | a0001c0002t0001g0336 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+11446C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621471 | ||||||
chr2:241621530
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1240+11387A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621530 | ||||||
chr2:241621585
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+11332G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621585 | ||||||
chr2:241621608
|
G | GA | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+11308dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621608 | ||||||
chr2:241621617
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+11300C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621617 | ||||||
chr2:241621632
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0064a0001c0001t0001g0066others(1): Show | 5 | HG02145.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+11285C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621632 | ||||||
chr2:241621664
|
C | T | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+11253G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621664 | ||||||
chr2:241621695
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1240+11222T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621695 | ||||||
chr2:241621708
|
G | C | 1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1240+11209C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621708 | ||||||
chr2:241621871
|
G | A | 1 | a0001c0002t0001g0357 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1240+11046C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621871 | ||||||
chr2:241622054
|
C | G | 2 | a0001c0001t0001g0132a0002c0003t0001g0088 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1240+10863G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622054 | ||||||
chr2:241622059
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1240+10858T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622059 | ||||||
chr2:241622096
|
G | A | 144 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(141): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1240+10821C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622096 | ||||||
chr2:241622288
|
A | C | 140 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(137): Show | 145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+10629T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622288 | ||||||
chr2:241622595
|
C | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 233 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1240+10322G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622595 | ||||||
chr2:241622596
|
A | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 9 | HG01099.hp1 HG02145.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+10321T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622596 | ||||||
chr2:241622746
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1240+10171A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622746 | ||||||
chr2:241622883
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+10034C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622883 | ||||||
chr2:241622960
|
G | A | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1240+9957C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622960 | ||||||
chr2:241623297
|
T | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+9620A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623297 | ||||||
chr2:241623385
|
G | C | 1 | a0002c0004t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+9532C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623385 | ||||||
chr2:241623451
|
G | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0069others(54): Show | 63 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1240+9466C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623451 | ||||||
chr2:241623593
|
G | GA | 39 | a0001c0001t0001g0066a0001c0002t0001g0002a0001c0002t0001g0003others(36): Show | 43 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1240+9323dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623593 | ||||||
chr2:241623607
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0029others(47): Show | 53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1240+9310C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623607 | ||||||
chr2:241623616
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+9301G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623616 | ||||||
chr2:241624025
|
G | A | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+8892C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624025 | ||||||
chr2:241624101
|
C | T | 5 | a0001c0002t0001g0107a0001c0002t0001g0108a0002c0004t0001g0075others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+8816G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624101 | ||||||
chr2:241624150
|
A | G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+8767T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624150 | ||||||
chr2:241624356
|
G | A | 3 | a0001c0002t0001g0107a0002c0004t0001g0075a0002c0004t0001g0078 | 3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1240+8561C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624356 | ||||||
chr2:241624430
|
T | C | 1 | a0001c0002t0001g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1240+8487A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624430 | ||||||
chr2:241624441
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1240+8476G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624441 | ||||||
chr2:241624442
|
G | A | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1240+8475C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624442 | ||||||
chr2:241624485
|
C | CA | 11 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 12 | HG02055.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240+8431dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624485 | ||||||
chr2:241624485
|
CA | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0054others(12): Show | 16 | HG01099.hp1 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240+8431delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624485 | ||||||
chr2:241624598
|
T | C | 4 | a0001c0002t0001g0306a0001c0002t0001g0307a0001c0002t0001g0308others(1): Show | 4 | HG00408.hp1 NA18972.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+8319A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624598 | ||||||
chr2:241624739
|
G | A | 2 | a0002c0004t0003g0162a0002c0004t0003g0163 | 2 | HG01261.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1240+8178C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624739 | ||||||
chr2:241624887
|
G | A | 1 | a0001c0002t0001g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1240+8030C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624887 | ||||||
chr2:241624956
|
G | A | 31 | a0001c0002t0001g0276a0001c0002t0001g0310a0001c0002t0001g0311others(28): Show | 31 | HG00438.hp2 HG01928.hp2 HG01993.hp2 others(28): Show |
intron_variant | MODIFIER | c.1240+7961C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624956 | ||||||
chr2:241625196
|
C | T | 2 | a0002c0004t0001g0164a0002c0004t0001g0169 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1240+7721G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625196 | ||||||
chr2:241625332
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1240+7585G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625332 | ||||||
chr2:241625444
|
T | C | 2 | a0001c0002t0001g0200a0001c0002t0001g0201 | 2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1240+7473A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625444 | ||||||
chr2:241625481
|
CA | C | 149 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1240+7435delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625481 | ||||||
chr2:241625481
|
CAAAAAAA | C | 7 | a0001c0002t0001g0322a0001c0002t0001g0323a0001c0002t0001g0324others(4): Show | 7 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+7429_1240+743 others(11): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625481 | ||||||
chr2:241625495
|
AAAAAGG | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+7416_1240+742 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625495 | ||||||
chr2:241625711
|
T | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+7206A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625711 | ||||||
chr2:241625797
|
C | CA | 32 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0040others(29): Show | 36 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1240+7119dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | ||||||
chr2:241625797
|
C | CAA | 10 | a0001c0001t0001g0058a0001c0002t0001g0202a0001c0002t0001g0209others(7): Show | 10 | HG00642.hp1 HG00741.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+7118_1240+711 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | ||||||
chr2:241625797
|
CA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1240+7119delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | ||||||
chr2:241625797
|
CAA | C | 44 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0069others(41): Show | 50 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1240+7118_1240+711 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | ||||||
chr2:241625807
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0002t0001g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1240+7092_1240+710 others(22): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625807 | ||||||
chr2:241625813
|
A | AG | 89 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(86): Show | 89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1240+7103_1240+710 others(5): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625813 | ||||||
chr2:241625813
|
A | G | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1240+7104T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625813 | ||||||
chr2:241625818
|
A | G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+7099T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625818 | ||||||
chr2:241625819
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1240+7098T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625819 | ||||||
chr2:241625820
|
A | G | 4 | a0001c0001t0001g0271a0002c0003t0001g0020a0002c0003t0001g0260others(1): Show | 5 | HG02559.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+7097T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625820 | ||||||
chr2:241625845
|
A | G | 1 | a0002c0003t0001g0176 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+7072T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625845 | ||||||
chr2:241626038
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1240+6879T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626038 | ||||||
chr2:241626116
|
G | C | 2 | a0001c0002t0001g0198a0001c0002t0001g0199 | 2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+6801C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626116 | ||||||
chr2:241626223
|
A | G | 1 | a0001c0002t0001g0281 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1240+6694T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626223 | ||||||
chr2:241626224
|
T | C | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+6693A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626224 | ||||||
chr2:241626383
|
G | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+6534C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626383 | ||||||
chr2:241626490
|
C | T | 1 | a0002c0004t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+6427G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626490 | ||||||
chr2:241626570
|
G | GT | 7 | a0001c0001t0001g0018a0001c0001t0001g0234a0001c0001t0001g0246others(4): Show | 8 | HG01106.hp1 HG01255.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+6346dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626570 | ||||||
chr2:241626572
|
T | G | 10 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 11 | HG02055.hp1 HG02818.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240+6345A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626572 | ||||||
chr2:241626614
|
A | G | 1 | a0002c0004t0001g0238 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1240+6303T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626614 | ||||||
chr2:241626753
|
A | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1240+6164T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626753 | ||||||
chr2:241626762
|
C | G | 93 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+6155G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626762 | ||||||
chr2:241626762
|
C | T | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+6155G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626762 | ||||||
chr2:241626888
|
T | A | 1 | a0002c0003t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1240+6029A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626888 | ||||||
chr2:241626946
|
CAT | C | 3 | a0001c0002t0001g0107a0002c0004t0001g0075a0002c0004t0001g0078 | 3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1240+5969_1240+597 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626946 | ||||||
chr2:241627148
|
T | C | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1240+5769A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627148 | ||||||
chr2:241627178
|
T | C | 95 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(92): Show | 95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+5739A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627178 | ||||||
chr2:241627291
|
T | C | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+5626A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627291 | ||||||
chr2:241627439
|
C | A | 5 | a0002c0004t0003g0158a0002c0004t0003g0159a0002c0004t0003g0160others(2): Show | 5 | HG01081.hp1 HG01123.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+5478G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627439 | ||||||
chr2:241627490
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1240+5427G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627490 | ||||||
chr2:241627792
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1240+5125G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627792 | ||||||
chr2:241627934
|
A | G | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+4983T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627934 | ||||||
chr2:241627955
|
T | C | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+4962A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627955 | ||||||
chr2:241628060
|
T | G | 1 | a0003c0007t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+4857A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628060 | ||||||
chr2:241628115
|
A | G | 1 | a0002c0003t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1240+4802T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628115 | ||||||
chr2:241628234
|
CCT | C | 44 | a0001c0001t0001g0018a0001c0001t0001g0069a0001c0001t0001g0070others(41): Show | 49 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1240+4681_1240+468 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628234 | ||||||
chr2:241628602
|
G | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0069others(54): Show | 63 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1240+4315C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628602 | ||||||
chr2:241628736
|
C | CA | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 55 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1240+4180dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628736 | ||||||
chr2:241628740
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0002t0001g0149 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1240+4162_1240+417 others(19): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628740 | ||||||
chr2:241628747
|
A | C | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+4170T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628747 | ||||||
chr2:241628748
|
CAAAAAAC others(10): Show |
C | 3 | a0001c0002t0001g0150a0001c0002t0001g0151a0001c0002t0001g0152 | 3 | NA18963.hp2 NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1240+4152_1240+416 others(21): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628748 | ||||||
chr2:241628769
|
A | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA18979.hp2 NA19010.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1240+4148T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628769 | ||||||
chr2:241628925
|
C | CA | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(103): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1240+3991dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | ||||||
chr2:241628925
|
C | CAA | 17 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0136others(14): Show | 18 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+3990_1240+399 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | ||||||
chr2:241628925
|
CA | C | 141 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(138): Show | 147 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1240+3991delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | ||||||
chr2:241628925
|
CAAAA | C | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+3988_1240+399 others(8): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | ||||||
chr2:241629125
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1240+3792G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629125 | ||||||
chr2:241629234
|
C | G | 1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1240+3683G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629234 | ||||||
chr2:241629287
|
T | C | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+3630A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629287 | ||||||
chr2:241629312
|
A | T | 7 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+3605T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629312 | ||||||
chr2:241629347
|
T | C | 92 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(89): Show | 92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1240+3570A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629347 | ||||||
chr2:241629385
|
G | C | 358 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(355): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.1240+3532C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629385 | ||||||
chr2:241629386
|
G | A | 2 | a0001c0001t0001g0141a0002c0003t0001g0081 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+3531C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629386 | ||||||
chr2:241629463
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244 | 5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+3454G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629463 | ||||||
chr2:241629472
|
TA | T | 109 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(106): Show | 109 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1240+3444delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629472 | ||||||
chr2:241629929
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1240+2988T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629929 | ||||||
chr2:241629936
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1240+2981C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629936 | ||||||
chr2:241629960
|
T | G | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+2957A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629960 | ||||||
chr2:241630146
|
T | C | 1 | a0003c0007t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+2771A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630146 | ||||||
chr2:241630153
|
T | A | 1 | a0002c0003t0001g0194 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1240+2764A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630153 | ||||||
chr2:241630198
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0210 | 4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+2719C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630198 | ||||||
chr2:241630215
|
C | T | 2 | a0002c0005t0001g0153a0002c0005t0001g0154 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+2702G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630215 | ||||||
chr2:241630266
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1240+2651C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630266 | ||||||
chr2:241630269
|
G | A | 1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1240+2648C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630269 | ||||||
chr2:241630376
|
C | CA | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+2540dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630376 | ||||||
chr2:241630401
|
C | A | 138 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(135): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1240+2516G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630401 | ||||||
chr2:241630456
|
A | C | 2 | a0001c0002t0001g0343a0001c0002t0001g0344 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1240+2461T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630456 | ||||||
chr2:241630473
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1240+2444C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630473 | ||||||
chr2:241630482
|
T | A | 238 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 253 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1240+2435A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630482 | ||||||
chr2:241630690
|
A | AATTGCTT others(25): Show |
1 | a0001c0001t0001g0054 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1240+2195_1240+222 others(36): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630690 | ||||||
chr2:241630779
|
C | CA | 32 | a0001c0001t0001g0047a0001c0001t0001g0129a0001c0001t0001g0147others(29): Show | 33 | HG00438.hp2 HG01928.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.1240+2137dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630779 | ||||||
chr2:241630779
|
CA | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0125others(7): Show | 10 | HG01099.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+2137delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630779 | ||||||
chr2:241630964
|
T | C | 6 | a0001c0001t0001g0048a0001c0001t0002g0049a0001c0001t0002g0050others(3): Show | 6 | HG01981.hp1 HG02293.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+1953A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630964 | ||||||
chr2:241631026
|
C | T | 139 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(136): Show | 144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1240+1891G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631026 | ||||||
chr2:241631030
|
C | T | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+1887G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631030 | ||||||
chr2:241631043
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG02132.hp2 NA18957.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+1874C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631043 | ||||||
chr2:241631051
|
C | T | 6 | a0001c0001t0001g0014a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 7 | HG01099.hp1 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+1866G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631051 | ||||||
chr2:241631199
|
G | A | 1 | a0001c0002t0001g0340 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1240+1718C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631199 | ||||||
chr2:241631204
|
G | A | 2 | a0001c0002t0001g0343a0001c0002t0001g0344 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1240+1713C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631204 | ||||||
chr2:241631297
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1240+1620A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631297 | ||||||
chr2:241631424
|
T | C | 182 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1240+1493A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631424 | ||||||
chr2:241631716
|
C | T | 33 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0200others(30): Show | 37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+1201G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631716 | ||||||
chr2:241631809
|
G | T | 9 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(6): Show | 9 | HG02056.hp2 HG02523.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240+1108C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631809 | ||||||
chr2:241631816
|
A | G | 4 | a0001c0002t0001g0198a0001c0002t0001g0199a0002c0005t0001g0153others(1): Show | 4 | HG03209.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+1101T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631816 | ||||||
chr2:241631868
|
T | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+1049A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631868 | ||||||
chr2:241631952
|
AAG | A | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+963_1240+964d others(4): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631952 | ||||||
chr2:241631967
|
G | A | 137 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(134): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1240+950C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631967 | ||||||
chr2:241632130
|
T | C | 1 | a0002c0003t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1240+787A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632130 | ||||||
chr2:241632133
|
C | T | 9 | a0001c0002t0001g0025a0001c0002t0001g0281a0001c0002t0001g0282others(6): Show | 9 | HG00639.hp1 HG01175.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+784G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632133 | ||||||
chr2:241632279
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1240+638A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632279 | ||||||
chr2:241632313
|
T | C | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1240+604A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632313 | ||||||
chr2:241632320
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1240+597C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632320 | ||||||
chr2:241632422
|
A | G | 137 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(134): Show | 142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1240+495T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632422 | ||||||
chr2:241632442
|
A | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(36): Show | 41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+475T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632442 | ||||||
chr2:241632487
|
C | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(36): Show | 41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+430G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632487 | ||||||
chr2:241632610
|
A | G | 1 | a0001c0002t0001g0197 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1240+307T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632610 | ||||||
chr2:241632638
|
G | A | 1 | a0002c0003t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1240+279C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632638 | ||||||
chr2:241632639
|
G | C | 1 | a0002c0003t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1240+278C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632639 | ||||||
chr2:241632800
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1240+117A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632800 | ||||||
chr2:241632847
|
G | A | 21 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0202others(18): Show | 25 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1240+70C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632847 | ||||||
chr2:241632881
|
G | A | 1 | a0001c0002t0001g0149 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1240+36C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632881 | ||||||
chr2:241632883
|
A | G | 1 | a0001c0002t0001g0149 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1240+34T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632883 | ||||||
chr2:241634101
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.78-22C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634101 | ||||||
chr2:241634102
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.78-23A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634102 | ||||||
chr2:241634103
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.78-24T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634103 | ||||||
chr2:241634182
|
C | T | 1 | a0001c0002t0001g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.78-103G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634182 | ||||||
chr2:241634214
|
C | A | 1 | a0001c0002t0001g0148 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.78-135G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634214 | ||||||
chr2:241634228
|
G | A | 1 | a0002c0004t0001g0238 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.78-149C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634228 | ||||||
chr2:241634231
|
C | T | 2 | a0002c0004t0001g0009a0002c0004t0001g0072 | 3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.78-152G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634231 | ||||||
chr2:241634277
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.78-198C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634277 | ||||||
chr2:241634353
|
T | C | 3 | a0001c0002t0001g0342a0001c0002t0001g0343a0001c0002t0001g0344 | 3 | HG02559.hp1 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.78-274A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634353 | ||||||
chr2:241634494
|
G | T | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.78-415C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634494 | ||||||
chr2:241634495
|
C | T | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.78-416G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634495 | ||||||
chr2:241634562
|
G | C | 4 | a0001c0002t0001g0149a0001c0002t0001g0150a0001c0002t0001g0151others(1): Show | 4 | NA18963.hp2 NA18967.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-483C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634562 | ||||||
chr2:241634796
|
T | C | 5 | a0001c0002t0001g0345a0001c0002t0001g0346a0001c0002t0001g0347others(2): Show | 5 | HG02040.hp1 HG02071.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-717A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634796 | ||||||
chr2:241634894
|
A | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 170 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.78-815T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634894 | ||||||
chr2:241635088
|
C | T | 86 | a0001c0002t0001g0276a0001c0002t0001g0281a0001c0002t0001g0282others(83): Show | 86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.78-1009G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635088 | ||||||
chr2:241635257
|
C | G | 3 | a0001c0002t0001g0351a0001c0002t0001g0352a0001c0002t0001g0353 | 3 | NA18948.hp2 NA19007.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.78-1178G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635257 | ||||||
chr2:241635330
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01516.hp1 HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.78-1251T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635330 | ||||||
chr2:241635391
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.78-1312C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635391 | ||||||
chr2:241635416
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.78-1337T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635416 | ||||||
chr2:241635604
|
C | T | 1 | a0002c0003t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77+1337G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635604 | ||||||
chr2:241635797
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.77+1144G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635797 | ||||||
chr2:241635807
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 10 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+1134T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635807 | ||||||
chr2:241635850
|
G | C | 1 | a0002c0003t0001g0242 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.77+1091C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635850 | ||||||
chr2:241635876
|
G | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 7 | HG01934.hp2 NA18960.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+1065C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635876 | ||||||
chr2:241635886
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02074.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.77+1055A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635886 | ||||||
chr2:241636141
|
T | C | 33 | a0001c0001t0001g0005a0001c0001t0001g0246a0001c0001t0001g0247others(30): Show | 36 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.77+800A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636141 | ||||||
chr2:241636386
|
G | A | 7 | a0001c0002t0001g0351a0001c0002t0001g0352a0001c0002t0001g0353others(4): Show | 7 | NA18939.hp2 NA18948.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+555C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636386 | ||||||
chr2:241636401
|
G | A | 87 | a0001c0002t0001g0276a0001c0002t0001g0281a0001c0002t0001g0282others(84): Show | 87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.77+540C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636401 | ||||||
chr2:241636545
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.77+396C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636545 | ||||||
chr2:241636648
|
G | A | 1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.77+293C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636648 | ||||||
chr2:241636697
|
C | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(38): Show | 43 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.77+244G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636697 | ||||||
chr2:241636701
|
C | T | 1 | a0002c0004t0001g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+240G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636701 | ||||||
chr2:241636719
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.77+222C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636719 | ||||||
chr2:241636853
|
G | C | 1 | a0001c0002t0001g0361 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.77+88C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636853 |