Item | Value |
---|---|
geneid | 84108 |
ensemblid | ENSG00000156374.16 |
hgncid | 21156 |
symbol | PCGF6 |
name | polycomb group ring finger 6 |
refseq_nuc | NM_001011663.2 |
refseq_prot | NP_001011663.1 |
ensembl_nuc | ENST00000369847.4 |
ensembl_prot | ENSP00000358862.3 |
mane_status | MANE Select |
chr | chr10 |
start | 103302796 |
end | 103351140 |
strand | - |
ver | v1.2 |
region | chr10:103302796-103351140 |
region5000 | chr10:103297796-103356140 |
regionname0 | PCGF6_chr10_103302796_103351140 |
regionname5000 | PCGF6_chr10_103297796_103356140 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 350 | 200 | 64 | 39 | 83 | 6 | 7 | 57 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002 | 0/1 | 352 | 170 | 27 | 31 | 77 | 10 | 24 | 59 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0003 | 0/0 | 352 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0004 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1053 | 200 | 64 | 39 | 83 | 6 | 7 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
c0002 | 0/1 | 1059 | 169 | 26 | 31 | 77 | 10 | 24 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
c0003 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
c0004 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
c0005 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1184 | 314 | 72 | 59 | 138 | 14 | 29 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0002 | 0/0 | 1184 | 20 | 1 | 8 | 6 | 2 | 3 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0003 | 0/0 | 1184 | 19 | 16 | 3 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0004 | 0/0 | 1184 | 15 | 0 | 0 | 15 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0005 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0006 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0007 | 0/0 | 1184 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
t0008 | 0/0 | 1184 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1053 | 200 | 64 | 39 | 83 | 6 | 7 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
a0002c0002 | 0/1 | 1059 | 169 | 26 | 31 | 77 | 10 | 24 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
a0002c0004 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
a0003c0003 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 | |
a0004c0005 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2236 | 181 | 48 | 36 | 83 | 6 | 7 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0001c0001t0003 | 0/0 | 2236 | 18 | 15 | 3 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0001c0001t0008 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0002t0001 | 0/1 | 2242 | 132 | 23 | 23 | 55 | 8 | 22 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0002t0002 | 0/0 | 2242 | 19 | 1 | 8 | 6 | 2 | 2 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0002t0004 | 0/0 | 2242 | 15 | 0 | 0 | 15 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0002t0005 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0002t0006 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0002t0007 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0002c0004t0001 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0003c0003t0002 | 0/0 | 2242 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
a0004c0005t0003 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | copy fasta | chr10 | 103297796 | 103356140 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0001c0001t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0002t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0002c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
a0004c0005t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0033 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0141 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0168 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0134 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00423 | hp1 | a0002 | c0002 | t0004 | g0016 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0160 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0101 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0135 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0059 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0060 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02257 | hp1 | a0002 | c0002 | t0006 | g0086 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0137 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02723 | hp1 | a0004 | c0005 | t0003 | g0364 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0225 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03654 | hp2 | a0003 | c0003 | t0002 | g0132 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0120 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0140 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0095 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0039 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0076 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18940 | hp1 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18943 | hp2 | a0002 | c0002 | t0004 | g0030 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18945 | hp1 | a0002 | c0002 | t0004 | g0027 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18946 | hp2 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18953 | hp2 | a0002 | c0002 | t0004 | g0043 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18962 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18963 | hp2 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18971 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18977 | hp2 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0073 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18983 | hp1 | a0002 | c0002 | t0004 | g0023 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18984 | hp1 | a0002 | c0002 | t0004 | g0031 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19011 | hp2 | a0002 | c0002 | t0007 | g0078 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19081 | hp1 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20129 | hp1 | a0002 | c0004 | t0001 | g0009 | AFR | ASW | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | ASW | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02109 | hp1 | a0002 | c0002 | t0005 | g0008 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0099 | REF | REF | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0230 | REF | REF | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103326595 | G | A | 1 | a0003 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.848C>T | p.Ala283Val | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/10 | 922/2236 | 848/1053 | 283/350 | chr10 | 103326595 | ||
chr10:103350766 | T | A | 1 | a0004 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.301A>T | p.Met101Leu | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/10 | 375/2236 | 301/1053 | 101/350 | chr10 | 103350766 | ||
chr10:103350983 | A | AGGAGGC | 2 | a0002a0003 | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
disruptive_inframe_insertion | MODERATE | c.78_83dupGCCTCC | p.Pro27_Pro28dup | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/10 | 157/2236 | 83/1053 | 28/350 | chr10 | 103350983 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103348946 | T | C | 1 | a0002c0004 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.414A>G | p.Lys138Lys | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 2/10 | 488/2236 | 414/1053 | 138/350 | chr10 | 103348946 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103302929 | G | A | 2 | a0001c0001t0003a0004c0005t0003 | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*976C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 976 | chr10 | 103302929 | |||||
chr10:103303099 | A | G | 1 | a0002c0002t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 806 | chr10 | 103303099 | |||||
chr10:103303339 | C | A | 1 | a0001c0001t0008 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*566G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 566 | chr10 | 103303339 | |||||
chr10:103303522 | T | C | 2 | a0002c0002t0002a0003c0003t0002 | 20 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*383A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 383 | chr10 | 103303522 | |||||
chr10:103303866 | G | T | 1 | a0002c0002t0006 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 39 | chr10 | 103303866 | |||||
chr10:103303879 | C | T | 1 | a0002c0002t0004 | 15 | HG00423.hp1 NA18940.hp1 NA18943.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 26 | chr10 | 103303879 | |||||
chr10:103351099 | C | T | 1 | a0002c0002t0005 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/10 | 33 | chr10 | 103351099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:103304046 | T | C | 1 | a0004c0005t0003g0364 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.997-85A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304046 | ||||||
chr10:103304140 | C | CT | 176 | a0001c0001t0001g0244a0001c0001t0001g0251a0001c0001t0001g0320others(173): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.997-180dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304140 | ||||||
chr10:103304537 | T | C | 173 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.997-576A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304537 | ||||||
chr10:103304656 | C | CT | 353 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.997-696dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304656 | ||||||
chr10:103304656 | C | CTT | 6 | a0001c0001t0001g0184a0001c0001t0001g0219a0002c0002t0001g0046others(3): Show | 6 | HG00621.hp2 HG02258.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.997-697_997-696dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304656 | ||||||
chr10:103304758 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.997-797G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304758 | ||||||
chr10:103304854 | C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0324 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.997-893G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304854 | ||||||
chr10:103304888 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.997-927C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304888 | ||||||
chr10:103305058 | G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0282 | 2 | NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.997-1097C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305058 | ||||||
chr10:103305140 | A | T | 1 | a0002c0002t0004g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.997-1179T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305140 | ||||||
chr10:103305140 | ATT | A | 23 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(20): Show | 24 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.997-1181_997-1180d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305140 | ||||||
chr10:103305216 | AC | A | 99 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0068others(96): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.997-1256delG | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305216 | ||||||
chr10:103305217 | C | G | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.997-1256G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305217 | ||||||
chr10:103305442 | C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.997-1481G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305442 | ||||||
chr10:103305553 | G | T | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.997-1592C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305553 | ||||||
chr10:103305610 | TAA | T | 4 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-1651_997-1650d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305610 | ||||||
chr10:103305652 | C | T | 185 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.997-1691G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305652 | ||||||
chr10:103305802 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.997-1841G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305802 | ||||||
chr10:103305850 | C | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG02809.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.997-1889G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305850 | ||||||
chr10:103305994 | T | G | 2 | a0002c0002t0001g0122a0002c0002t0001g0164 | 2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.997-2033A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305994 | ||||||
chr10:103306040 | T | G | 1 | a0002c0002t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.997-2079A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306040 | ||||||
chr10:103306088 | C | CA | 173 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.997-2128_997-2127i others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306088 | ||||||
chr10:103306102 | C | CT | 48 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(45): Show | 50 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.997-2142dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306102 | ||||||
chr10:103306102 | CT | C | 9 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0223others(6): Show | 9 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.997-2142delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306102 | ||||||
chr10:103306260 | G | A | 1 | a0002c0002t0001g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.997-2299C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306260 | ||||||
chr10:103306557 | T | C | 35 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(32): Show | 37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.997-2596A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306557 | ||||||
chr10:103306564 | C | T | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.997-2603G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306564 | ||||||
chr10:103306705 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.997-2744G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306705 | ||||||
chr10:103306758 | G | C | 1 | a0002c0002t0001g0099 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.997-2797C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306758 | ||||||
chr10:103306828 | G | A | 15 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(12): Show | 15 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.997-2867C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306828 | ||||||
chr10:103306830 | G | T | 1 | a0002c0002t0001g0010 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.997-2869C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306830 | ||||||
chr10:103306876 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.997-2915C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306876 | ||||||
chr10:103306981 | A | G | 2 | a0002c0002t0002g0134a0002c0002t0002g0135 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.997-3020T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306981 | ||||||
chr10:103307190 | C | A | 3 | a0002c0002t0001g0111a0002c0002t0001g0158a0002c0002t0001g0159 | 3 | NA18959.hp2 NA18980.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.997-3229G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307190 | ||||||
chr10:103307280 | T | C | 207 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(204): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.997-3319A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307280 | ||||||
chr10:103307460 | G | C | 4 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0146others(1): Show | 4 | NA18951.hp1 NA19012.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-3499C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307460 | ||||||
chr10:103307465 | AAAGT | A | 4 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0029others(1): Show | 4 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-3508_997-3505d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307465 | ||||||
chr10:103307517 | C | T | 2 | a0002c0002t0001g0097a0002c0002t0001g0162 | 2 | HG01167.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.997-3556G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307517 | ||||||
chr10:103307847 | T | G | 1 | a0002c0002t0001g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.997-3886A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307847 | ||||||
chr10:103308078 | A | T | 1 | a0002c0002t0001g0060 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.997-4117T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308078 | ||||||
chr10:103308098 | A | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0307 | 2 | HG00609.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.997-4137T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308098 | ||||||
chr10:103308169 | T | C | 1 | a0002c0002t0001g0146 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.997-4208A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308169 | ||||||
chr10:103308462 | G | A | 2 | a0002c0002t0001g0109a0002c0002t0001g0128 | 2 | HG02809.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.997-4501C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308462 | ||||||
chr10:103308476 | G | A | 1 | a0002c0002t0001g0168 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.997-4515C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308476 | ||||||
chr10:103308503 | A | G | 1 | a0002c0002t0001g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.997-4542T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308503 | ||||||
chr10:103308510 | T | C | 19 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.997-4549A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308510 | ||||||
chr10:103308568 | T | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02818.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.997-4607A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308568 | ||||||
chr10:103308660 | C | G | 6 | a0002c0002t0001g0054a0002c0002t0001g0061a0002c0002t0001g0062others(3): Show | 6 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.997-4699G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308660 | ||||||
chr10:103309140 | G | T | 11 | a0002c0002t0001g0042a0002c0002t0001g0046a0002c0002t0001g0047others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.996+5046C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309140 | ||||||
chr10:103309196 | T | TG | 53 | a0001c0001t0001g0178a0001c0001t0001g0218a0001c0001t0001g0244others(50): Show | 55 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.996+4989dupC | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309196 | ||||||
chr10:103309197 | G | T | 22 | a0001c0001t0001g0007a0001c0001t0001g0247a0001c0001t0001g0249others(19): Show | 23 | HG01361.hp1 HG01928.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.996+4989C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309197 | ||||||
chr10:103309363 | A | C | 173 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.996+4823T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309363 | ||||||
chr10:103309482 | G | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(10): Show | 14 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.996+4704C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309482 | ||||||
chr10:103309775 | A | T | 1 | a0002c0002t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.996+4411T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309775 | ||||||
chr10:103309954 | C | CT | 8 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+4231dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309954 | ||||||
chr10:103309954 | C | CTT | 35 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(32): Show | 37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.996+4230_996+4231d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309954 | ||||||
chr10:103309954 | CT | C | 17 | a0001c0001t0001g0222a0001c0001t0001g0294a0001c0001t0001g0340others(14): Show | 17 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+4231delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309954 | ||||||
chr10:103310116 | A | G | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0222others(4): Show | 7 | HG02622.hp1 HG02896.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.996+4070T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310116 | ||||||
chr10:103310189 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.996+3997A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310189 | ||||||
chr10:103310203 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.996+3983G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310203 | ||||||
chr10:103310228 | A | C | 1 | a0002c0002t0001g0018 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.996+3958T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310228 | ||||||
chr10:103310229 | G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0311a0001c0001t0001g0313others(1): Show | 4 | HG01952.hp2 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+3957C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310229 | ||||||
chr10:103310496 | T | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0218others(60): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.996+3690A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310496 | ||||||
chr10:103310630 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.996+3556G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310630 | ||||||
chr10:103310903 | G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0245a0001c0001t0001g0246others(5): Show | 9 | HG00423.hp2 NA18612.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.996+3283C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310903 | ||||||
chr10:103311001 | A | T | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.996+3185T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311001 | ||||||
chr10:103311080 | C | T | 35 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(32): Show | 37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.996+3106G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311080 | ||||||
chr10:103311084 | T | A | 19 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.996+3102A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311084 | ||||||
chr10:103311205 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.996+2981C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311205 | ||||||
chr10:103311325 | A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0209 | 2 | HG00673.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.996+2861T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311325 | ||||||
chr10:103311414 | T | C | 1 | a0002c0002t0001g0097 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.996+2772A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311414 | ||||||
chr10:103311447 | C | CT | 6 | a0001c0001t0001g0246a0001c0001t0001g0344a0002c0002t0001g0010others(3): Show | 6 | HG00544.hp1 HG00597.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+2738dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311447 | ||||||
chr10:103311447 | CT | C | 11 | a0001c0001t0001g0235a0001c0001t0001g0273a0001c0001t0001g0318others(8): Show | 11 | HG00438.hp1 HG00558.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.996+2738delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311447 | ||||||
chr10:103311812 | C | G | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.996+2374G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311812 | ||||||
chr10:103312084 | C | CA | 178 | a0001c0001t0001g0172a0001c0001t0001g0187a0001c0001t0001g0190others(175): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.996+2101dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312084 | ||||||
chr10:103312084 | C | CAA | 30 | a0001c0001t0001g0211a0001c0001t0001g0351a0001c0001t0001g0352others(27): Show | 30 | HG00621.hp1 HG01261.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.996+2100_996+2101d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312084 | ||||||
chr10:103312253 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.996+1933G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312253 | ||||||
chr10:103312272 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.996+1914T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312272 | ||||||
chr10:103312561 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.996+1625G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312561 | ||||||
chr10:103312687 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.996+1499G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312687 | ||||||
chr10:103312773 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.996+1413G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312773 | ||||||
chr10:103312829 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.996+1357G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312829 | ||||||
chr10:103312944 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.996+1242C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312944 | ||||||
chr10:103312959 | T | TCAAAAA | 50 | a0001c0001t0001g0344a0001c0001t0003g0191a0001c0001t0003g0192others(47): Show | 52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.996+1221_996+1226d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | ||||||
chr10:103312959 | T | TCAAAAAC others(5): Show |
12 | a0002c0002t0001g0066a0002c0002t0004g0012a0002c0002t0004g0020others(9): Show | 12 | HG00673.hp1 NA18943.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.996+1215_996+1226d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | ||||||
chr10:103312959 | T | TCAAAAAC others(11): Show |
1 | a0002c0002t0004g0021 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.996+1209_996+1226d others(20): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | ||||||
chr10:103312959 | TCAAAAA | T | 111 | a0001c0001t0001g0219a0001c0001t0001g0240a0001c0001t0001g0248others(108): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.996+1221_996+1226d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | ||||||
chr10:103312959 | TCAAAAAC others(11): Show |
T | 1 | a0002c0002t0001g0155 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.996+1209_996+1226d others(20): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | ||||||
chr10:103313047 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.996+1139G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313047 | ||||||
chr10:103313154 | T | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.996+1032A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313154 | ||||||
chr10:103313313 | C | T | 103 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0041others(100): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.996+873G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313313 | ||||||
chr10:103313495 | G | T | 12 | a0001c0001t0001g0182a0001c0001t0001g0209a0001c0001t0001g0210others(9): Show | 12 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.996+691C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313495 | ||||||
chr10:103313575 | A | T | 1 | a0001c0001t0001g0267 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.996+611T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313575 | ||||||
chr10:103313617 | G | GA | 19 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.996+568dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313617 | ||||||
chr10:103313677 | G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0189 | 3 | HG02559.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.996+509C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313677 | ||||||
chr10:103313716 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.996+470A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313716 | ||||||
chr10:103313858 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.996+328A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313858 | ||||||
chr10:103314511 | T | G | 1 | a0002c0002t0001g0148 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.910-239A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314511 | ||||||
chr10:103314574 | CATTA | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0224others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-306_910-303del others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314574 | ||||||
chr10:103314628 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.910-356T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314628 | ||||||
chr10:103314797 | A | G | 4 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-525T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314797 | ||||||
chr10:103314954 | T | TA | 126 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0222others(123): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.910-683dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | ||||||
chr10:103314954 | T | TAA | 62 | a0001c0001t0001g0185a0001c0001t0001g0189a0001c0001t0001g0266others(59): Show | 63 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.910-684_910-683dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | ||||||
chr10:103314954 | T | TAAA | 9 | a0001c0001t0001g0184a0001c0001t0003g0207a0001c0001t0003g0208others(6): Show | 9 | HG01433.hp1 HG01433.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.910-685_910-683dup others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | ||||||
chr10:103314954 | TA | T | 67 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0173others(64): Show | 69 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.910-683delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | ||||||
chr10:103314955 | A | T | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910-683T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314955 | ||||||
chr10:103315093 | T | C | 12 | a0002c0002t0001g0161a0002c0002t0004g0012a0002c0002t0004g0020others(9): Show | 12 | NA18943.hp2 NA18945.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-821A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315093 | ||||||
chr10:103315261 | T | C | 2 | a0002c0002t0001g0169a0002c0002t0001g0170 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.910-989A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315261 | ||||||
chr10:103315314 | T | C | 5 | a0002c0002t0001g0001a0002c0002t0001g0033a0002c0002t0001g0038others(2): Show | 7 | HG00099.hp1 HG00280.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-1042A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315314 | ||||||
chr10:103315318 | T | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG02886.hp1 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.910-1046A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315318 | ||||||
chr10:103315560 | T | C | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.910-1288A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315560 | ||||||
chr10:103315585 | T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-1313A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315585 | ||||||
chr10:103315718 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.910-1446C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315718 | ||||||
chr10:103315955 | C | T | 102 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0041others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.910-1683G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315955 | ||||||
chr10:103315968 | A | ATG | 7 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0001g0239others(4): Show | 7 | HG01891.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-1698_910-1697d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315968 | ||||||
chr10:103315968 | ATG | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(25): Show | 29 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.910-1698_910-1697d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315968 | ||||||
chr10:103315968 | ATGTG | A | 8 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(5): Show | 8 | HG01099.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-1700_910-1697d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315968 | ||||||
chr10:103315981 | T | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(21): Show | 25 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.910-1709A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315981 | ||||||
chr10:103315983 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.910-1711A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315983 | ||||||
chr10:103315990 | GTGTGTA | G | 5 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG02809.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1724_910-1719d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315990 | ||||||
chr10:103315992 | G | A | 7 | a0001c0001t0001g0188a0001c0001t0001g0222a0001c0001t0001g0350others(4): Show | 7 | HG02896.hp1 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-1720C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315992 | ||||||
chr10:103315992 | G | GTA | 5 | a0001c0001t0001g0231a0001c0001t0003g0196a0001c0001t0003g0198others(2): Show | 5 | HG01081.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-1721_910-1720i others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315992 | ||||||
chr10:103315994 | G | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(71): Show | 77 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.910-1722C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | ||||||
chr10:103315994 | G | GTA | 4 | a0002c0002t0004g0012a0002c0002t0004g0021a0002c0002t0004g0022others(1): Show | 4 | NA18940.hp1 NA18963.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1724_910-1723d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | ||||||
chr10:103315994 | G | GTGTA | 4 | a0002c0002t0001g0010a0002c0002t0001g0019a0002c0002t0001g0066others(1): Show | 4 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-1723_910-1722i others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | ||||||
chr10:103315994 | GTA | G | 62 | a0001c0001t0001g0241a0001c0001t0001g0253a0001c0001t0001g0304others(59): Show | 63 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.910-1724_910-1723d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | ||||||
chr10:103315994 | GTATA | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0218others(30): Show | 35 | HG00423.hp2 HG00609.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.910-1726_910-1723d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | ||||||
chr10:103315996 | A | G | 29 | a0001c0001t0001g0238a0001c0001t0001g0292a0001c0001t0001g0299others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.910-1724T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315996 | ||||||
chr10:103315997 | TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.910-1745_910-1726d others(22): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315997 | ||||||
chr10:103315998 | A | G | 7 | a0001c0001t0001g0253a0001c0001t0001g0299a0002c0002t0001g0013others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-1726T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315998 | ||||||
chr10:103316000 | A | G | 5 | a0002c0002t0001g0054a0002c0002t0001g0061a0002c0002t0001g0062others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1728T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316000 | ||||||
chr10:103316009 | T | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0179a0001c0001t0001g0181others(3): Show | 6 | HG00733.hp2 HG00738.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-1737A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316009 | ||||||
chr10:103316009 | TATATAGA others(7): Show |
T | 4 | a0001c0001t0001g0262a0001c0001t0001g0311a0001c0001t0001g0313others(1): Show | 4 | HG01952.hp2 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1751_910-1738d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316009 | ||||||
chr10:103316011 | T | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0174a0001c0001t0001g0175others(24): Show | 28 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.910-1739A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316011 | ||||||
chr10:103316011 | TATAG | T | 53 | a0001c0001t0001g0242a0001c0001t0001g0248a0001c0001t0001g0249others(50): Show | 53 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.910-1743_910-1740d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316011 | ||||||
chr10:103316011 | TATAGAGA others(3): Show |
T | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.910-1749_910-1740d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316011 | ||||||
chr10:103316013 | T | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(75): Show | 79 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.910-1741A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316013 | T | TAG | 3 | a0001c0001t0003g0197a0001c0001t0003g0201a0001c0001t0003g0205 | 3 | HG01074.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.910-1743_910-1742d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316013 | T | TAGAGAG | 3 | a0001c0001t0003g0193a0001c0001t0003g0204a0001c0001t0003g0207 | 3 | HG02717.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.910-1747_910-1742d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316013 | T | TATAG | 3 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0001g0353 | 3 | HG03041.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.910-1742_910-1741i others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316013 | TAG | T | 21 | a0001c0001t0001g0292a0001c0001t0001g0335a0001c0001t0001g0341others(18): Show | 22 | HG00323.hp1 HG00558.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.910-1743_910-1742d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316013 | TAGAG | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0243a0001c0001t0001g0244others(31): Show | 35 | HG00408.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.910-1745_910-1742d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316013 | TAGAGAGA others(5): Show |
T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.910-1753_910-1742d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | ||||||
chr10:103316015 | G | T | 53 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0210others(50): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.910-1743C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316015 | ||||||
chr10:103316017 | G | T | 31 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0224others(28): Show | 33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.910-1745C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316017 | ||||||
chr10:103316019 | G | T | 19 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0224others(16): Show | 19 | HG01175.hp1 HG01192.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.910-1747C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316019 | ||||||
chr10:103316021 | G | T | 5 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0224others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1749C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316021 | ||||||
chr10:103316023 | G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0190 | 2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.910-1751C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316023 | ||||||
chr10:103316237 | T | C | 3 | a0002c0002t0002g0125a0002c0002t0002g0126a0002c0002t0002g0151 | 3 | HG00741.hp1 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.910-1965A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316237 | ||||||
chr10:103316567 | T | C | 1 | a0002c0002t0007g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.910-2295A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316567 | ||||||
chr10:103316626 | C | T | 12 | a0002c0002t0001g0001a0002c0002t0001g0011a0002c0002t0001g0028others(9): Show | 14 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2354G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316626 | ||||||
chr10:103316967 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.910-2695A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316967 | ||||||
chr10:103317367 | C | A | 172 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.910-3095G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317367 | ||||||
chr10:103317693 | T | C | 1 | a0002c0002t0001g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.910-3421A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317693 | ||||||
chr10:103317763 | G | GT | 13 | a0001c0001t0001g0231a0002c0002t0001g0054a0002c0002t0001g0055others(10): Show | 13 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.910-3492dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317763 | ||||||
chr10:103317764 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.910-3492A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317764 | ||||||
chr10:103317787 | G | A | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.910-3515C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317787 | ||||||
chr10:103317886 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.910-3614C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317886 | ||||||
chr10:103318038 | T | C | 1 | a0002c0002t0001g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.910-3766A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318038 | ||||||
chr10:103318046 | C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0166 | 2 | HG02056.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.910-3774G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318046 | ||||||
chr10:103318209 | G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.910-3937C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318209 | ||||||
chr10:103318212 | A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.910-3940T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318212 | ||||||
chr10:103318213 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-3941G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318213 | ||||||
chr10:103318218 | A | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.910-3946T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318218 | ||||||
chr10:103318398 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.910-4126C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318398 | ||||||
chr10:103318466 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.910-4194G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318466 | ||||||
chr10:103318472 | C | T | 1 | a0002c0002t0002g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.910-4200G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318472 | ||||||
chr10:103318692 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.910-4420A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318692 | ||||||
chr10:103318707 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.910-4435C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318707 | ||||||
chr10:103318775 | G | C | 4 | a0002c0002t0004g0020a0002c0002t0004g0024a0002c0002t0004g0031others(1): Show | 4 | NA18971.hp1 NA18982.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-4503C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318775 | ||||||
chr10:103318868 | C | T | 5 | a0002c0002t0001g0011a0002c0002t0001g0028a0002c0002t0001g0032others(2): Show | 5 | HG00639.hp1 HG00738.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-4596G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318868 | ||||||
chr10:103318944 | T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0209 | 2 | HG00673.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.910-4672A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318944 | ||||||
chr10:103319036 | T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(22): Show | 26 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-4764A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319036 | ||||||
chr10:103319373 | G | A | 12 | a0002c0002t0001g0001a0002c0002t0001g0011a0002c0002t0001g0028others(9): Show | 14 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-5101C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319373 | ||||||
chr10:103319402 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.910-5130G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319402 | ||||||
chr10:103319405 | C | T | 172 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.910-5133G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319405 | ||||||
chr10:103319660 | T | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0218others(60): Show | 65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.910-5388A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319660 | ||||||
chr10:103319682 | T | C | 172 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.910-5410A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319682 | ||||||
chr10:103319855 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.910-5583A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319855 | ||||||
chr10:103319979 | T | C | 1 | a0002c0002t0001g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.910-5707A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319979 | ||||||
chr10:103320262 | A | G | 3 | a0002c0002t0001g0093a0002c0002t0001g0106a0002c0002t0001g0107 | 3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.910-5990T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320262 | ||||||
chr10:103320358 | A | G | 1 | a0002c0002t0002g0160 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.910-6086T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320358 | ||||||
chr10:103320555 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.909+5979G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320555 | ||||||
chr10:103320624 | T | C | 19 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+5910A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320624 | ||||||
chr10:103320690 | C | CA | 11 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0223others(8): Show | 11 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.909+5843dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320690 | ||||||
chr10:103320745 | T | G | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.909+5789A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320745 | ||||||
chr10:103320748 | G | C | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.909+5786C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320748 | ||||||
chr10:103320818 | T | C | 232 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(229): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.909+5716A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320818 | ||||||
chr10:103320930 | T | A | 4 | a0002c0002t0004g0020a0002c0002t0004g0024a0002c0002t0004g0031others(1): Show | 4 | NA18971.hp1 NA18982.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+5604A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320930 | ||||||
chr10:103321348 | A | G | 12 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056others(9): Show | 12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+5186T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103321348 | ||||||
chr10:103321670 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.909+4864G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103321670 | ||||||
chr10:103322148 | G | T | 1 | a0002c0002t0001g0100 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.909+4386C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322148 | ||||||
chr10:103322174 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.909+4360C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322174 | ||||||
chr10:103322175 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.909+4359C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322175 | ||||||
chr10:103322349 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.909+4185C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322349 | ||||||
chr10:103322426 | A | G | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+4108T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322426 | ||||||
chr10:103322784 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.909+3750T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322784 | ||||||
chr10:103322822 | T | TCA | 3 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0005g0008 | 3 | HG02109.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.909+3710_909+3711d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322822 | ||||||
chr10:103322878 | C | CA | 22 | a0001c0001t0001g0339a0001c0001t0001g0346a0001c0001t0003g0191others(19): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.909+3655dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322878 | ||||||
chr10:103322900 | A | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0224others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+3634T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322900 | ||||||
chr10:103322903 | C | A | 9 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0223others(6): Show | 9 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+3631G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322903 | ||||||
chr10:103322904 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.909+3630T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322904 | ||||||
chr10:103323114 | A | G | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+3420T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323114 | ||||||
chr10:103323175 | T | C | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+3359A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323175 | ||||||
chr10:103323225 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+3309T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323225 | ||||||
chr10:103323249 | T | C | 1 | a0002c0002t0001g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.909+3285A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323249 | ||||||
chr10:103323422 | A | C | 1 | a0002c0002t0001g0092 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.909+3112T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323422 | ||||||
chr10:103323422 | A | G | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+3112T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323422 | ||||||
chr10:103323469 | T | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0275a0001c0001t0001g0304 | 3 | HG02129.hp2 NA18939.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.909+3065A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323469 | ||||||
chr10:103323531 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.909+3003C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323531 | ||||||
chr10:103323614 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.909+2920A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323614 | ||||||
chr10:103323660 | T | C | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+2874A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323660 | ||||||
chr10:103324130 | G | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0324 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.909+2404C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324130 | ||||||
chr10:103324146 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.909+2388G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324146 | ||||||
chr10:103324328 | GA | G | 152 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(149): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.909+2205delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324328 | ||||||
chr10:103324328 | GAA | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(23): Show | 27 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+2204_909+2205d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324328 | ||||||
chr10:103324329 | A | AAAAAAAA others(316): Show |
2 | a0001c0001t0003g0202a0001c0001t0003g0207 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.909+2204_909+2205i others(325): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324329 | ||||||
chr10:103324329 | A | AAAAAAAA others(315): Show |
14 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(11): Show | 14 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+2204_909+2205i others(324): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324329 | ||||||
chr10:103324329 | A | AAAAAAAA others(314): Show |
2 | a0001c0001t0003g0195a0001c0001t0003g0200 | 2 | HG01081.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.909+2204_909+2205i others(323): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324329 | ||||||
chr10:103324330 | A | AAAAAAAA others(314): Show |
1 | a0004c0005t0003g0364 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.909+2203_909+2204i others(323): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324330 | ||||||
chr10:103324450 | C | T | 11 | a0002c0002t0001g0042a0002c0002t0001g0046a0002c0002t0001g0047others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+2084G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324450 | ||||||
chr10:103324535 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.909+1999C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324535 | ||||||
chr10:103324562 | G | C | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+1972C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324562 | ||||||
chr10:103324599 | A | T | 1 | a0001c0001t0001g0213 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.909+1935T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324599 | ||||||
chr10:103324637 | G | A | 12 | a0001c0001t0001g0182a0001c0001t0001g0209a0001c0001t0001g0210others(9): Show | 12 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+1897C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324637 | ||||||
chr10:103324685 | G | A | 1 | a0002c0002t0001g0145 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.909+1849C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324685 | ||||||
chr10:103324692 | G | A | 5 | a0002c0002t0002g0101a0002c0002t0002g0125a0002c0002t0002g0126others(2): Show | 5 | HG00741.hp1 HG00741.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+1842C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324692 | ||||||
chr10:103324759 | C | CA | 20 | a0001c0001t0001g0217a0001c0001t0001g0244a0001c0001t0001g0247others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.909+1774dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324759 | ||||||
chr10:103324759 | CA | C | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1774delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324759 | ||||||
chr10:103324774 | C | A | 1 | a0002c0002t0004g0026 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.909+1760G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324774 | ||||||
chr10:103324775 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.909+1759G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324775 | ||||||
chr10:103324775 | C | CA | 27 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0003g0191others(24): Show | 27 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+1758dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324775 | ||||||
chr10:103324776 | A | C | 1 | a0002c0002t0004g0026 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.909+1758T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324776 | ||||||
chr10:103324812 | C | T | 3 | a0002c0002t0001g0100a0002c0002t0001g0149a0002c0002t0007g0078 | 3 | NA18955.hp2 NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.909+1722G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324812 | ||||||
chr10:103324891 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.909+1643A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324891 | ||||||
chr10:103325043 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.909+1491C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325043 | ||||||
chr10:103325050 | G | A | 8 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(5): Show | 8 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1484C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325050 | ||||||
chr10:103325060 | G | A | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1474C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325060 | ||||||
chr10:103325067 | G | A | 7 | a0002c0002t0001g0002a0002c0002t0001g0091a0002c0002t0001g0092others(4): Show | 8 | HG01934.hp1 HG02273.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1467C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325067 | ||||||
chr10:103325083 | C | T | 153 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(150): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.909+1451G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325083 | ||||||
chr10:103325124 | G | C | 4 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG02886.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1410C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325124 | ||||||
chr10:103325142 | T | TAAATA | 49 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(46): Show | 50 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.909+1387_909+1391d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | ||||||
chr10:103325142 | T | TAAATAAA others(3): Show |
25 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(22): Show | 25 | HG01074.hp1 HG01081.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.909+1382_909+1391d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | ||||||
chr10:103325142 | T | TAAATAAA others(8): Show |
1 | a0001c0001t0003g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.909+1377_909+1391d others(17): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | ||||||
chr10:103325142 | TAAATA | T | 150 | a0001c0001t0001g0221a0002c0002t0001g0001a0002c0002t0001g0002others(147): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.909+1387_909+1391d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | ||||||
chr10:103325142 | TAAATAAA others(3): Show |
T | 3 | a0002c0002t0001g0015a0002c0002t0001g0054a0002c0002t0001g0063 | 3 | HG01109.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.909+1382_909+1391d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | ||||||
chr10:103325277 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.909+1257C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325277 | ||||||
chr10:103325414 | C | T | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+1120G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325414 | ||||||
chr10:103325434 | T | C | 53 | a0002c0002t0001g0069a0002c0002t0001g0072a0002c0002t0001g0077others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.909+1100A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325434 | ||||||
chr10:103325493 | C | A | 1 | a0002c0002t0001g0158 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.909+1041G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325493 | ||||||
chr10:103325539 | C | T | 19 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+995G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325539 | ||||||
chr10:103325605 | C | T | 3 | a0002c0002t0001g0093a0002c0002t0001g0106a0002c0002t0001g0107 | 3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.909+929G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325605 | ||||||
chr10:103325852 | T | TA | 52 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(49): Show | 53 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.909+681dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | ||||||
chr10:103325852 | TA | T | 8 | a0001c0001t0001g0231a0001c0001t0001g0239a0001c0001t0001g0273others(5): Show | 8 | HG01070.hp1 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+681delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | ||||||
chr10:103325852 | TAA | T | 164 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.909+680_909+681del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | ||||||
chr10:103325852 | TAAA | T | 7 | a0002c0002t0001g0088a0002c0002t0001g0093a0002c0002t0001g0094others(4): Show | 7 | HG00733.hp1 HG01433.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+679_909+681del others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | ||||||
chr10:103326018 | A | C | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+516T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326018 | ||||||
chr10:103326022 | CCT | C | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG02071.hp2 HG02074.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+510_909+511del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326022 | ||||||
chr10:103326198 | CCA | C | 19 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+334_909+335del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326198 | ||||||
chr10:103326302 | T | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG02809.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+232A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326302 | ||||||
chr10:103326305 | C | T | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+229G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326305 | ||||||
chr10:103326385 | T | C | 4 | a0001c0001t0001g0323a0001c0001t0001g0333a0001c0001t0001g0345others(1): Show | 4 | HG01361.hp1 HG01934.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+149A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326385 | ||||||
chr10:103326388 | C | CA | 35 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(32): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.909+145dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326388 | ||||||
chr10:103326436 | A | G | 1 | a0001c0001t0001g0334 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.909+98T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326436 | ||||||
chr10:103326655 | C | T | 10 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0223others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.811-23G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103326655 | ||||||
chr10:103326776 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.811-144A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103326776 | ||||||
chr10:103326953 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.811-321G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103326953 | ||||||
chr10:103327129 | A | G | 11 | a0002c0002t0004g0012a0002c0002t0004g0020a0002c0002t0004g0023others(8): Show | 11 | NA18943.hp2 NA18945.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.811-497T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327129 | ||||||
chr10:103327204 | G | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0312 | 2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.811-572C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327204 | ||||||
chr10:103327246 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.811-614A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327246 | ||||||
chr10:103327354 | G | T | 1 | a0002c0002t0001g0114 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.811-722C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327354 | ||||||
chr10:103327545 | T | G | 1 | a0002c0002t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.811-913A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327545 | ||||||
chr10:103327625 | C | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0224others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-993G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327625 | ||||||
chr10:103327799 | C | T | 2 | a0002c0002t0001g0046a0002c0002t0001g0047 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.811-1167G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327799 | ||||||
chr10:103327825 | C | G | 12 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056others(9): Show | 12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.811-1193G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327825 | ||||||
chr10:103327841 | A | AT | 12 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0014others(9): Show | 14 | HG00099.hp1 HG00280.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.811-1210dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327841 | ||||||
chr10:103327841 | AT | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(38): Show | 42 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.811-1210delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327841 | ||||||
chr10:103327910 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.811-1278G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327910 | ||||||
chr10:103327922 | G | A | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-1290C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327922 | ||||||
chr10:103328035 | T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.811-1403A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328035 | ||||||
chr10:103328183 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.811-1551G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328183 | ||||||
chr10:103328235 | A | G | 1 | a0002c0002t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.811-1603T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328235 | ||||||
chr10:103328354 | A | G | 1 | a0002c0002t0001g0148 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.811-1722T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328354 | ||||||
chr10:103328536 | T | A | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.811-1904A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328536 | ||||||
chr10:103328714 | T | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0324 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.811-2082A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328714 | ||||||
chr10:103328855 | G | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0222others(4): Show | 7 | HG02622.hp1 HG02896.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.811-2223C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328855 | ||||||
chr10:103328879 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.811-2247C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328879 | ||||||
chr10:103328947 | G | A | 1 | a0002c0002t0001g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.811-2315C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328947 | ||||||
chr10:103328994 | C | A | 1 | a0001c0001t0003g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.811-2362G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328994 | ||||||
chr10:103329150 | C | T | 2 | a0002c0002t0002g0134a0002c0002t0002g0135 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.811-2518G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329150 | ||||||
chr10:103329166 | A | G | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-2534T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329166 | ||||||
chr10:103329189 | G | A | 1 | a0002c0002t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.811-2557C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329189 | ||||||
chr10:103329204 | C | T | 3 | a0002c0002t0004g0021a0002c0002t0004g0022a0002c0002t0004g0036 | 3 | NA18940.hp1 NA18977.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.811-2572G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329204 | ||||||
chr10:103329222 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.811-2590A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329222 | ||||||
chr10:103329260 | A | G | 1 | a0001c0001t0001g0349 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.811-2628T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329260 | ||||||
chr10:103329334 | C | A | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-2702G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329334 | ||||||
chr10:103329335 | C | A | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-2703G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329335 | ||||||
chr10:103329446 | C | T | 4 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-2814G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329446 | ||||||
chr10:103329541 | G | A | 5 | a0001c0001t0001g0233a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.811-2909C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329541 | ||||||
chr10:103329661 | C | T | 3 | a0002c0002t0001g0093a0002c0002t0001g0106a0002c0002t0001g0107 | 3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.811-3029G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329661 | ||||||
chr10:103329736 | G | A | 2 | a0002c0002t0001g0041a0002c0002t0001g0051 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.811-3104C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329736 | ||||||
chr10:103329741 | G | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0226 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.811-3109C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329741 | ||||||
chr10:103329769 | G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0324 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.811-3137C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329769 | ||||||
chr10:103329771 | C | T | 3 | a0002c0002t0001g0093a0002c0002t0001g0106a0002c0002t0001g0107 | 3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.811-3139G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329771 | ||||||
chr10:103329990 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.811-3358G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329990 | ||||||
chr10:103330135 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.811-3503G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330135 | ||||||
chr10:103330487 | T | TA | 9 | a0001c0001t0003g0202a0002c0002t0001g0010a0002c0002t0001g0017others(6): Show | 9 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.810+3437dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330487 | ||||||
chr10:103330733 | G | A | 1 | a0001c0001t0001g0347 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.810+3192C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330733 | ||||||
chr10:103330757 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.810+3168C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330757 | ||||||
chr10:103330823 | G | T | 1 | a0002c0002t0002g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.810+3102C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330823 | ||||||
chr10:103330825 | A | G | 1 | a0002c0002t0001g0118 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.810+3100T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330825 | ||||||
chr10:103330948 | C | T | 1 | a0002c0002t0001g0074 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.810+2977G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330948 | ||||||
chr10:103331242 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.810+2683C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331242 | ||||||
chr10:103331446 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.810+2479A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331446 | ||||||
chr10:103331616 | A | T | 9 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(6): Show | 9 | HG02071.hp2 HG02074.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.810+2309T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331616 | ||||||
chr10:103331631 | T | A | 9 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0223others(6): Show | 9 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.810+2294A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331631 | ||||||
chr10:103331645 | G | A | 10 | a0001c0001t0001g0183a0001c0001t0001g0190a0001c0001t0001g0223others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.810+2280C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331645 | ||||||
chr10:103331702 | A | C | 52 | a0002c0002t0001g0069a0002c0002t0001g0072a0002c0002t0001g0079others(49): Show | 52 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.810+2223T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331702 | ||||||
chr10:103332216 | G | T | 15 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(12): Show | 15 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+1709C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332216 | ||||||
chr10:103332337 | T | C | 1 | a0002c0002t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.810+1588A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332337 | ||||||
chr10:103332542 | C | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.810+1383G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332542 | ||||||
chr10:103332579 | T | C | 4 | a0001c0001t0001g0251a0001c0001t0001g0335a0001c0001t0001g0342others(1): Show | 4 | HG00558.hp2 HG02027.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+1346A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332579 | ||||||
chr10:103332690 | T | C | 232 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(229): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.810+1235A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332690 | ||||||
chr10:103332704 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.810+1221A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332704 | ||||||
chr10:103332854 | C | G | 1 | a0002c0002t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.810+1071G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332854 | ||||||
chr10:103332975 | G | A | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.810+950C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332975 | ||||||
chr10:103333032 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.810+893A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333032 | ||||||
chr10:103333117 | T | TA | 25 | a0001c0001t0001g0229a0001c0001t0001g0246a0001c0001t0001g0354others(22): Show | 25 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.810+807dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333117 | ||||||
chr10:103333117 | TA | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0172others(79): Show | 84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.810+807delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333117 | ||||||
chr10:103333557 | T | C | 1 | a0001c0001t0001g0338 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.810+368A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333557 | ||||||
chr10:103333814 | C | T | 1 | a0001c0001t0001g0344 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.810+111G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333814 | ||||||
chr10:103333834 | T | A | 1 | a0002c0002t0001g0088 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.810+91A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333834 | ||||||
chr10:103334261 | G | T | 3 | a0002c0002t0001g0093a0002c0002t0001g0106a0002c0002t0001g0107 | 3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.783-309C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103334261 | ||||||
chr10:103334642 | T | G | 2 | a0002c0002t0001g0041a0002c0002t0001g0051 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.783-690A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103334642 | ||||||
chr10:103334646 | G | C | 1 | a0001c0001t0001g0361 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.783-694C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103334646 | ||||||
chr10:103335091 | T | A | 3 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0005g0008 | 3 | HG02109.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.783-1139A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335091 | ||||||
chr10:103335216 | T | TA | 14 | a0001c0001t0001g0182a0001c0001t0001g0209a0001c0001t0001g0210others(11): Show | 14 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.783-1265dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335216 | ||||||
chr10:103335216 | TA | T | 6 | a0001c0001t0001g0235a0001c0001t0001g0312a0001c0001t0001g0350others(3): Show | 6 | HG01070.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.783-1265delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335216 | ||||||
chr10:103335366 | A | AT | 6 | a0001c0001t0001g0210a0001c0001t0001g0318a0001c0001t0001g0355others(3): Show | 6 | HG00609.hp1 HG01192.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.783-1415dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335366 | ||||||
chr10:103335423 | G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0317a0002c0002t0001g0011 | 3 | HG00099.hp2 HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.783-1471C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335423 | ||||||
chr10:103335447 | T | C | 173 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.783-1495A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335447 | ||||||
chr10:103335488 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.783-1536C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335488 | ||||||
chr10:103335709 | T | C | 8 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0049others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.783-1757A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335709 | ||||||
chr10:103335827 | T | C | 173 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.783-1875A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335827 | ||||||
chr10:103335892 | G | A | 2 | a0002c0002t0001g0087a0002c0002t0001g0096 | 2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.783-1940C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335892 | ||||||
chr10:103335941 | C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0242a0001c0001t0001g0243others(55): Show | 59 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.783-1989G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335941 | ||||||
chr10:103335952 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.783-2000G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335952 | ||||||
chr10:103336229 | G | A | 1 | a0002c0002t0001g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.783-2277C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336229 | ||||||
chr10:103336245 | T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.783-2293A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336245 | ||||||
chr10:103336247 | T | A | 1 | a0002c0002t0001g0088 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.783-2295A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336247 | ||||||
chr10:103336248 | A | T | 8 | a0001c0001t0001g0253a0002c0002t0001g0054a0002c0002t0001g0061others(5): Show | 8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-2296T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336248 | ||||||
chr10:103336264 | A | G | 103 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0041others(100): Show | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.783-2312T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336264 | ||||||
chr10:103336806 | C | T | 15 | a0002c0002t0004g0012a0002c0002t0004g0016a0002c0002t0004g0020others(12): Show | 15 | HG00423.hp1 NA18940.hp1 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.783-2854G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336806 | ||||||
chr10:103336970 | G | C | 1 | a0002c0002t0001g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.783-3018C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336970 | ||||||
chr10:103337274 | C | G | 1 | a0002c0002t0001g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.783-3322G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337274 | ||||||
chr10:103337428 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.783-3476G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337428 | ||||||
chr10:103337608 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783-3656A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337608 | ||||||
chr10:103337638 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.783-3686C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337638 | ||||||
chr10:103337765 | TAAAAATA others(307): Show |
T | 173 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.783-4127_783-3814d others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337765 | ||||||
chr10:103337831 | G | A | 12 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056others(9): Show | 12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.783-3879C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337831 | ||||||
chr10:103338063 | CA | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0172others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.783-4112delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338063 | ||||||
chr10:103338063 | CAA | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0246a0001c0001t0001g0252others(2): Show | 6 | NA18612.hp2 NA18951.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.783-4113_783-4112d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338063 | ||||||
chr10:103338134 | G | A | 1 | a0002c0002t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.783-4182C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338134 | ||||||
chr10:103338155 | T | C | 1 | a0002c0002t0001g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.783-4203A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338155 | ||||||
chr10:103338267 | G | A | 100 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0068others(97): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.783-4315C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338267 | ||||||
chr10:103338277 | C | T | 3 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0204 | 3 | HG02280.hp1 HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.783-4325G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338277 | ||||||
chr10:103338380 | A | T | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.783-4428T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338380 | ||||||
chr10:103338384 | A | G | 1 | a0002c0002t0001g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783-4432T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338384 | ||||||
chr10:103338401 | C | A | 1 | a0001c0001t0003g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783-4449G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338401 | ||||||
chr10:103338402 | G | A | 4 | a0002c0002t0001g0054a0002c0002t0001g0062a0002c0002t0001g0063others(1): Show | 4 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-4450C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338402 | ||||||
chr10:103338470 | G | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0234 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.783-4518C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338470 | ||||||
chr10:103338544 | C | CA | 94 | a0001c0001t0001g0271a0002c0002t0001g0003a0002c0002t0001g0041others(91): Show | 95 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.783-4593dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338544 | ||||||
chr10:103338544 | C | CAA | 9 | a0002c0002t0001g0002a0002c0002t0001g0084a0002c0002t0001g0091others(6): Show | 10 | HG01934.hp1 HG02071.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.783-4594_783-4593d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338544 | ||||||
chr10:103338664 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.783-4712G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338664 | ||||||
chr10:103338725 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783-4773C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338725 | ||||||
chr10:103338740 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.783-4788G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338740 | ||||||
chr10:103338741 | G | A | 1 | a0002c0002t0002g0076 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.783-4789C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338741 | ||||||
chr10:103339054 | A | T | 1 | a0002c0002t0001g0019 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.783-5102T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339054 | ||||||
chr10:103339185 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.783-5233G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339185 | ||||||
chr10:103339431 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.783-5479G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339431 | ||||||
chr10:103339733 | G | A | 4 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+5291C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339733 | ||||||
chr10:103339752 | G | A | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+5272C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339752 | ||||||
chr10:103339766 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782+5258G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339766 | ||||||
chr10:103339801 | C | CA | 15 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0179others(12): Show | 15 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.782+5222dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339801 | ||||||
chr10:103339805 | AAAAAAAC others(6): Show |
A | 1 | a0002c0002t0001g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.782+5206_782+5218d others(15): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339805 | ||||||
chr10:103339806 | AAAAAACA others(3): Show |
A | 8 | a0001c0001t0001g0259a0002c0002t0001g0046a0002c0002t0001g0077others(5): Show | 8 | HG01071.hp1 HG01167.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+5208_782+5217d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | ||||||
chr10:103339806 | AAAAAACA others(5): Show |
A | 18 | a0002c0002t0001g0003a0002c0002t0001g0042a0002c0002t0001g0079others(15): Show | 19 | HG00544.hp2 HG01978.hp2 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.782+5206_782+5217d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | ||||||
chr10:103339806 | AAAAAACA others(7): Show |
A | 38 | a0002c0002t0001g0002a0002c0002t0001g0048a0002c0002t0001g0049others(35): Show | 39 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.782+5204_782+5217d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | ||||||
chr10:103339806 | AAAAAACA others(9): Show |
A | 9 | a0002c0002t0001g0047a0002c0002t0001g0087a0002c0002t0001g0141others(6): Show | 9 | HG00140.hp1 HG02738.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.782+5202_782+5217d others(18): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | ||||||
chr10:103339806 | AAAAAACA others(13): Show |
A | 4 | a0002c0002t0004g0020a0002c0002t0004g0024a0002c0002t0004g0031others(1): Show | 4 | NA18971.hp1 NA18982.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+5198_782+5217d others(22): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | ||||||
chr10:103339807 | AAAAACAC others(4): Show |
A | 8 | a0001c0001t0001g0260a0001c0001t0001g0272a0001c0001t0001g0283others(5): Show | 8 | HG00140.hp2 HG01361.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.782+5206_782+5216d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339807 | ||||||
chr10:103339807 | AAAAACAC others(6): Show |
A | 3 | a0001c0001t0001g0276a0001c0001t0001g0300a0001c0001t0001g0314 | 3 | HG01074.hp2 NA19077.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.782+5204_782+5216d others(15): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339807 | ||||||
chr10:103339807 | AAAAACAC others(14): Show |
A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0307others(1): Show | 4 | HG00609.hp2 NA18747.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+5196_782+5216d others(23): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339807 | ||||||
chr10:103339808 | AAAACACA others(1): Show |
A | 10 | a0001c0001t0003g0202a0002c0002t0001g0013a0002c0002t0001g0014others(7): Show | 10 | HG00099.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+5208_782+5215d others(10): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | ||||||
chr10:103339808 | AAAACACA others(3): Show |
A | 20 | a0002c0002t0001g0001a0002c0002t0001g0032a0002c0002t0001g0034others(17): Show | 22 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.782+5206_782+5215d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | ||||||
chr10:103339808 | AAAACACA others(5): Show |
A | 25 | a0001c0001t0001g0354a0001c0001t0003g0200a0002c0002t0001g0069others(22): Show | 25 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.782+5204_782+5215d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | ||||||
chr10:103339808 | AAAACACA others(7): Show |
A | 6 | a0002c0002t0002g0075a0002c0002t0002g0134a0002c0002t0002g0135others(3): Show | 6 | HG00323.hp2 HG00733.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.782+5202_782+5215d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | ||||||
chr10:103339808 | AAAACACA others(9): Show |
A | 1 | a0002c0002t0001g0124 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.782+5200_782+5215d others(18): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | ||||||
chr10:103339809 | AAACACAC | A | 16 | a0001c0001t0001g0185a0001c0001t0001g0242a0001c0001t0001g0244others(13): Show | 16 | HG01981.hp2 HG02040.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.782+5208_782+5214d others(9): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339809 | ||||||
chr10:103339809 | AAACACAC others(2): Show |
A | 9 | a0001c0001t0001g0261a0001c0001t0001g0264a0001c0001t0001g0273others(6): Show | 9 | HG01070.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.782+5206_782+5214d others(11): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339809 | ||||||
chr10:103339809 | AAACACAC others(4): Show |
A | 5 | a0001c0001t0001g0005a0001c0001t0001g0277a0001c0001t0001g0278others(2): Show | 6 | HG01516.hp1 HG01928.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.782+5204_782+5214d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339809 | ||||||
chr10:103339810 | A | C | 3 | a0001c0001t0001g0310a0002c0002t0001g0071a0002c0002t0001g0158 | 3 | HG00544.hp1 NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.782+5214T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AAC | A | 15 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0190others(12): Show | 15 | HG00323.hp1 HG00673.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.782+5212_782+5213d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACAC | A | 6 | a0001c0001t0001g0228a0001c0001t0001g0258a0001c0001t0001g0311others(3): Show | 6 | HG01106.hp2 HG01981.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.782+5210_782+5213d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACACAC | A | 11 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0241others(8): Show | 11 | HG00597.hp2 HG01952.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+5208_782+5213d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACACACA others(1): Show |
A | 11 | a0001c0001t0001g0240a0001c0001t0001g0313a0001c0001t0001g0320others(8): Show | 11 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+5206_782+5213d others(10): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACACACA others(3): Show |
A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0204 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.782+5204_782+5213d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACACACA others(5): Show |
A | 12 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196others(9): Show | 12 | HG01074.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.782+5202_782+5213d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0253a0001c0001t0001g0319 | 2 | NA18940.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.782+5198_782+5213d others(18): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339810 | AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0237a0001c0001t0001g0315 | 2 | NA18984.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.782+5196_782+5213d others(20): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | ||||||
chr10:103339811 | AC | A | 7 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0209others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.782+5212delG | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339811 | ACAC | A | 9 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0186others(6): Show | 9 | HG00642.hp2 HG02300.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.782+5210_782+5212d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339811 | ACACAC | A | 5 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0221others(2): Show | 5 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.782+5208_782+5212d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339811 | ACACACAC others(2): Show |
A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0243 | 3 | HG02135.hp2 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.782+5204_782+5212d others(11): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339811 | ACACACAC others(4): Show |
A | 2 | a0001c0001t0001g0247a0001c0001t0001g0342 | 2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.782+5202_782+5212d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339811 | ACACACAC others(8): Show |
A | 4 | a0001c0001t0001g0184a0001c0001t0001g0251a0001c0001t0001g0322others(1): Show | 4 | HG00558.hp2 HG02258.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+5198_782+5212d others(17): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339811 | ACACACAC others(10): Show |
A | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0218others(28): Show | 33 | HG00423.hp2 HG01257.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.782+5196_782+5212d others(19): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | ||||||
chr10:103339812 | C | A | 26 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0176others(23): Show | 26 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.782+5212G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339812 | ||||||
chr10:103339814 | C | A | 30 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183others(27): Show | 30 | HG00323.hp1 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.782+5210G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339814 | ||||||
chr10:103339816 | C | A | 22 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0183others(19): Show | 22 | HG00642.hp2 HG00735.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.782+5208G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339816 | ||||||
chr10:103339818 | C | A | 21 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0227others(18): Show | 21 | HG00438.hp2 HG00558.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.782+5206G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339818 | ||||||
chr10:103339820 | C | A | 16 | a0001c0001t0001g0229a0001c0001t0001g0320a0001c0001t0001g0321others(13): Show | 16 | HG00408.hp1 HG00438.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.782+5204G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339820 | ||||||
chr10:103339822 | C | A | 12 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056others(9): Show | 12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.782+5202G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339822 | ||||||
chr10:103339824 | C | A | 14 | a0001c0001t0001g0247a0001c0001t0001g0342a0002c0002t0001g0054others(11): Show | 14 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.782+5200G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339824 | ||||||
chr10:103339826 | C | A | 11 | a0002c0002t0001g0054a0002c0002t0001g0056a0002c0002t0001g0057others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.782+5198G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339826 | ||||||
chr10:103339828 | C | A | 11 | a0001c0001t0001g0251a0001c0001t0001g0319a0001c0001t0001g0322others(8): Show | 11 | HG00558.hp2 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.782+5196G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339828 | ||||||
chr10:103339830 | C | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0218others(28): Show | 33 | HG01257.hp2 HG01361.hp1 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.782+5194G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339830 | ||||||
chr10:103340007 | C | CA | 40 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(37): Show | 40 | HG00099.hp1 HG00408.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.782+5016dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340007 | ||||||
chr10:103340007 | C | CAA | 110 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(107): Show | 114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.782+5015_782+5016d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340007 | ||||||
chr10:103340007 | C | CAAA | 17 | a0002c0002t0001g0018a0002c0002t0001g0029a0002c0002t0001g0035others(14): Show | 17 | HG01192.hp1 HG01346.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.782+5014_782+5016d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340007 | ||||||
chr10:103340130 | T | C | 1 | a0001c0001t0001g0357 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.782+4894A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340130 | ||||||
chr10:103340180 | GA | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0176a0001c0001t0001g0177others(32): Show | 38 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.782+4843delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | ||||||
chr10:103340180 | GAA | G | 11 | a0001c0001t0001g0174a0001c0001t0001g0185a0001c0001t0001g0282others(8): Show | 11 | HG00733.hp2 HG01074.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+4842_782+4843d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | ||||||
chr10:103340180 | GAAA | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0242a0001c0001t0001g0256others(47): Show | 51 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.782+4841_782+4843d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | ||||||
chr10:103340180 | GAAAA | G | 58 | a0001c0001t0001g0255a0002c0002t0001g0002a0002c0002t0001g0041others(55): Show | 59 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.782+4840_782+4843d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | ||||||
chr10:103340194 | A | ATATAT | 3 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0029 | 3 | HG02486.hp1 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.782+4829_782+4830i others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340194 | ||||||
chr10:103340194 | A | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0071 | 2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.782+4830T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340194 | ||||||
chr10:103340196 | A | AAT | 7 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.782+4827_782+4828i others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | ||||||
chr10:103340196 | A | AT | 4 | a0001c0001t0003g0203a0001c0001t0003g0206a0001c0001t0003g0207others(1): Show | 4 | HG01169.hp1 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+4827_782+4828i others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | ||||||
chr10:103340196 | A | T | 31 | a0001c0001t0003g0191a0001c0001t0003g0202a0002c0002t0001g0010others(28): Show | 31 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.782+4828T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | ||||||
chr10:103340196 | AAAAT | A | 16 | a0002c0002t0001g0003a0002c0002t0001g0069a0002c0002t0001g0074others(13): Show | 17 | HG00323.hp2 HG00733.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.782+4824_782+4827d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | ||||||
chr10:103340197 | AAAT | A | 18 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0284others(15): Show | 18 | HG01884.hp1 HG01928.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.782+4824_782+4826d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340197 | ||||||
chr10:103340198 | A | ATATATAT others(10): Show |
1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+4825_782+4826i others(19): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | ||||||
chr10:103340198 | A | T | 85 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(82): Show | 87 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.782+4826T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | ||||||
chr10:103340198 | AAT | A | 28 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0186others(25): Show | 28 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.782+4824_782+4825d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | ||||||
chr10:103340198 | AATAT | A | 10 | a0001c0001t0001g0292a0001c0001t0001g0293a0002c0002t0001g0054others(7): Show | 10 | HG00323.hp1 HG00735.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+4822_782+4825d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | ||||||
chr10:103340199 | AT | A | 8 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0188others(5): Show | 8 | HG00642.hp2 HG00735.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+4824delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340199 | ||||||
chr10:103340199 | ATAT | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0183others(66): Show | 71 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.782+4822_782+4824d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340199 | ||||||
chr10:103340199 | ATATAT | A | 5 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0063others(2): Show | 5 | HG01109.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.782+4820_782+4824d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340199 | ||||||
chr10:103340200 | T | A | 9 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0213others(6): Show | 9 | HG00738.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.782+4824A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340200 | ||||||
chr10:103340202 | T | A | 23 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0182others(20): Show | 23 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.782+4822A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340202 | ||||||
chr10:103340204 | T | A | 56 | a0001c0001t0001g0007a0001c0001t0001g0182a0001c0001t0001g0187others(53): Show | 57 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.782+4820A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340204 | ||||||
chr10:103340206 | T | A | 10 | a0001c0001t0001g0354a0002c0002t0001g0054a0002c0002t0001g0055others(7): Show | 10 | HG01099.hp1 HG01109.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.782+4818A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340206 | ||||||
chr10:103340342 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.782+4682G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340342 | ||||||
chr10:103340396 | G | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+4628C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340396 | ||||||
chr10:103340600 | A | AT | 8 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+4423dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340600 | ||||||
chr10:103340600 | AT | A | 15 | a0001c0001t0001g0239a0001c0001t0001g0354a0002c0002t0001g0054others(12): Show | 15 | HG00735.hp1 HG01109.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.782+4423delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340600 | ||||||
chr10:103340700 | G | A | 1 | a0002c0002t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.782+4324C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340700 | ||||||
chr10:103340755 | G | T | 1 | a0002c0002t0001g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.782+4269C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340755 | ||||||
chr10:103340848 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.782+4176G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340848 | ||||||
chr10:103341210 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.782+3814G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341210 | ||||||
chr10:103341278 | C | T | 1 | a0002c0002t0001g0028 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.782+3746G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341278 | ||||||
chr10:103341609 | T | C | 1 | a0002c0002t0001g0141 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.782+3415A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341609 | ||||||
chr10:103341688 | C | T | 2 | a0002c0002t0001g0091a0002c0002t0001g0092 | 2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.782+3336G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341688 | ||||||
chr10:103341733 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.782+3291A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341733 | ||||||
chr10:103341798 | C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+3226G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341798 | ||||||
chr10:103341944 | C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(22): Show | 26 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.782+3080G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341944 | ||||||
chr10:103341955 | C | G | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+3069G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341955 | ||||||
chr10:103342018 | G | A | 4 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0015others(1): Show | 4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+3006C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342018 | ||||||
chr10:103342202 | C | T | 1 | a0001c0001t0001g0342 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.782+2822G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342202 | ||||||
chr10:103342223 | T | C | 2 | a0001c0001t0001g0299a0001c0001t0001g0341 | 2 | HG03239.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.782+2801A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342223 | ||||||
chr10:103342346 | G | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+2678C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342346 | ||||||
chr10:103342543 | T | C | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.782+2481A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342543 | ||||||
chr10:103342701 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.782+2323A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342701 | ||||||
chr10:103342776 | T | C | 1 | a0002c0002t0001g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.782+2248A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342776 | ||||||
chr10:103342788 | T | C | 1 | a0002c0002t0001g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.782+2236A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342788 | ||||||
chr10:103342919 | A | ATG | 353 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.782+2104_782+2105i others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342919 | ||||||
chr10:103342964 | T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+2060A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342964 | ||||||
chr10:103343007 | C | A | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.782+2017G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343007 | ||||||
chr10:103343208 | G | A | 102 | a0001c0001t0001g0258a0002c0002t0001g0002a0002c0002t0001g0003others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.782+1816C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343208 | ||||||
chr10:103343219 | C | T | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+1805G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343219 | ||||||
chr10:103343257 | C | T | 1 | a0002c0002t0004g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.782+1767G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343257 | ||||||
chr10:103343533 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.782+1491C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343533 | ||||||
chr10:103343797 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.782+1227G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343797 | ||||||
chr10:103343811 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.782+1213G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343811 | ||||||
chr10:103343832 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0347a0001c0001t0001g0350a0001c0001t0001g0357others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+1183_782+1191d others(11): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | ||||||
chr10:103343832 | C | CAAAAAAA others(3): Show |
184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0172others(181): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.782+1182_782+1191d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | ||||||
chr10:103343832 | C | CAAAAAAA others(4): Show |
94 | a0001c0001t0001g0006a0001c0001t0001g0173a0001c0001t0001g0180others(91): Show | 97 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.782+1181_782+1191d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | ||||||
chr10:103343832 | C | CAAAAAAA others(5): Show |
41 | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0190others(38): Show | 42 | HG00621.hp2 HG00639.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.782+1180_782+1191d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | ||||||
chr10:103343832 | C | CAAAAAAA others(6): Show |
16 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0251others(13): Show | 16 | HG00558.hp2 HG00735.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.782+1179_782+1191d others(15): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | ||||||
chr10:103343832 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0253a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | HG02027.hp1 NA18940.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.782+1178_782+1191d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | ||||||
chr10:103343847 | A | AAAAAAAA others(3): Show |
1 | a0002c0002t0004g0012 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.782+1176_782+1177i others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343847 | ||||||
chr10:103343941 | C | G | 1 | a0002c0002t0001g0088 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.782+1083G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343941 | ||||||
chr10:103343970 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.782+1054A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343970 | ||||||
chr10:103344166 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.782+858C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344166 | ||||||
chr10:103344273 | C | CT | 9 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0183others(6): Show | 9 | HG00735.hp2 HG01192.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.782+750dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344273 | ||||||
chr10:103344273 | CT | C | 21 | a0001c0001t0001g0241a0001c0001t0001g0347a0001c0001t0003g0191others(18): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.782+750delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344273 | ||||||
chr10:103344326 | C | T | 173 | a0001c0001t0001g0258a0001c0001t0003g0191a0001c0001t0003g0192others(170): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.782+698G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344326 | ||||||
chr10:103344365 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.782+659C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344365 | ||||||
chr10:103344668 | G | T | 186 | a0001c0001t0001g0258a0001c0001t0003g0191a0001c0001t0003g0192others(183): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.782+356C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344668 | ||||||
chr10:103344758 | C | T | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG02071.hp2 HG02155.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.782+266G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344758 | ||||||
chr10:103344766 | C | T | 1 | a0002c0002t0001g0011 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.782+258G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344766 | ||||||
chr10:103345155 | T | C | 1 | a0002c0002t0001g0010 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.674-23A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345155 | ||||||
chr10:103345273 | T | C | 2 | a0002c0002t0001g0158a0002c0002t0001g0159 | 2 | NA18959.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.674-141A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345273 | ||||||
chr10:103345496 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.674-364G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345496 | ||||||
chr10:103345508 | CT | C | 170 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(167): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.674-377delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345508 | ||||||
chr10:103345547 | G | A | 12 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056others(9): Show | 12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.674-415C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345547 | ||||||
chr10:103345949 | T | C | 3 | a0001c0001t0003g0206a0001c0001t0003g0207a0001c0001t0003g0208 | 3 | HG01891.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.674-817A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345949 | ||||||
chr10:103346197 | A | T | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0057others(3): Show | 6 | HG00735.hp1 HG01099.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+1041T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346197 | ||||||
chr10:103346222 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.673+1016A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346222 | ||||||
chr10:103346224 | G | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.673+1014C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346224 | ||||||
chr10:103346408 | G | A | 1 | a0002c0002t0002g0160 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.673+830C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346408 | ||||||
chr10:103347176 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.673+62T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103347176 | ||||||
chr10:103347636 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.558-186A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347636 | ||||||
chr10:103347681 | T | C | 1 | a0001c0001t0001g0362 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.558-231A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347681 | ||||||
chr10:103347707 | T | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.558-257A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347707 | ||||||
chr10:103347713 | G | A | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.558-263C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347713 | ||||||
chr10:103347721 | T | A | 1 | a0002c0002t0001g0065 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.558-271A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347721 | ||||||
chr10:103347819 | T | C | 1 | a0002c0002t0001g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.558-369A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347819 | ||||||
chr10:103347836 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.558-386C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347836 | ||||||
chr10:103347847 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.558-397G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347847 | ||||||
chr10:103347886 | G | A | 1 | a0001c0001t0001g0344 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.558-436C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347886 | ||||||
chr10:103347999 | T | G | 1 | a0001c0001t0001g0345 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.558-549A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347999 | ||||||
chr10:103348005 | TC | T | 352 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(349): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.558-556delG | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348005 | ||||||
chr10:103348333 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+383A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348333 | ||||||
chr10:103348334 | T | A | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+382A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348334 | ||||||
chr10:103348335 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+381A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348335 | ||||||
chr10:103348336 | T | G | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+380A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348336 | ||||||
chr10:103348337 | T | A | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+379A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348337 | ||||||
chr10:103348338 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+378A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348338 | ||||||
chr10:103348339 | T | A | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+377A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348339 | ||||||
chr10:103348340 | G | C | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+376C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348340 | ||||||
chr10:103348340 | GT | G | 162 | a0001c0001t0001g0354a0002c0002t0001g0001a0002c0002t0001g0002others(159): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.557+375delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348340 | ||||||
chr10:103348341 | T | G | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+375A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348341 | ||||||
chr10:103348342 | T | A | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+374A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348342 | ||||||
chr10:103348343 | T | C | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+373A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348343 | ||||||
chr10:103348344 | T | G | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+372A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348344 | ||||||
chr10:103348345 | T | A | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+371A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348345 | ||||||
chr10:103348347 | T | G | 1 | a0001c0001t0001g0346 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+369A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348347 | ||||||
chr10:103348687 | T | C | 1 | a0002c0002t0001g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.557+29A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348687 | ||||||
chr10:103348698 | T | C | 154 | a0002c0002t0001g0001a0002c0002t0001g0002a0002c0002t0001g0003others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.557+18A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348698 | ||||||
chr10:103348890 | G | A | 1 | a0002c0002t0001g0161 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.460+10C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 2/9 | chr10 | 103348890 | ||||||
chr10:103349117 | G | C | 1 | a0002c0002t0001g0053 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.361-118C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349117 | ||||||
chr10:103349154 | T | C | 1 | a0001c0001t0001g0347 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.361-155A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349154 | ||||||
chr10:103349404 | T | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.361-405A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349404 | ||||||
chr10:103349460 | T | C | 1 | a0002c0002t0001g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.361-461A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349460 | ||||||
chr10:103349479 | G | GT | 260 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(257): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.361-481dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349479 | ||||||
chr10:103349479 | G | GTT | 33 | a0001c0001t0001g0004a0001c0001t0001g0182a0001c0001t0001g0242others(30): Show | 34 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.361-482_361-481dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349479 | ||||||
chr10:103349479 | G | GTTT | 34 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(31): Show | 36 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.361-483_361-481dup others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349479 | ||||||
chr10:103349512 | CCT | C | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.361-515_361-514del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349512 | ||||||
chr10:103349711 | G | A | 1 | a0002c0002t0001g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.361-712C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349711 | ||||||
chr10:103350083 | A | AAAAAC | 12 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(9): Show | 13 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+619_360+623dup others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350083 | ||||||
chr10:103350083 | A | AAAAACAA others(3): Show |
2 | a0002c0002t0001g0068a0002c0002t0001g0069 | 2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.360+614_360+623dup others(10): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350083 | ||||||
chr10:103350176 | G | A | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.360+531C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350176 | ||||||
chr10:103350267 | C | CA | 114 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0351others(111): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.360+439dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350267 | ||||||
chr10:103350267 | C | CAA | 6 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0168others(3): Show | 6 | HG00280.hp1 HG01261.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+438_360+439dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350267 | ||||||
chr10:103350624 | C | G | 1 | a0002c0004t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.360+83G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350624 | ||||||
chr10:103350684 | G | A | 1 | a0001c0001t0001g0363 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.360+23C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350684 |