geneid | 5281 |
---|---|
ensemblid | ENSG00000151665.13 |
hgncid | 8962 |
symbol | PIGF |
name | phosphatidylinositol glycan anchor biosynthesis class F |
refseq_nuc | NM_002643.4 |
refseq_prot | NP_002634.1 |
ensembl_nuc | ENST00000281382.11 |
ensembl_prot | ENSP00000281382.6 |
mane_status | MANE Select |
chr | chr2 |
start | 46580937 |
end | 46617041 |
strand | - |
ver | v1.2 |
region | chr2:46580937-46617041 |
region5000 | chr2:46575937-46622041 |
regionname0 | PIGF_chr2_46580937_46617041 |
regionname5000 | PIGF_chr2_46575937_46622041 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 219 | 360 | 92 | 74 | 130 | 16 | 46 | 98 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0002 | 0/0 | 219 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0003 | 0/0 | 219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0004 | 0/0 | 219 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0005 | 0/0 | 219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0006 | 0/0 | 219 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 660 | 300 | 90 | 49 | 109 | 14 | 36 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
c0002 | 0/0 | 660 | 60 | 2 | 25 | 21 | 2 | 10 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
c0003 | 0/0 | 660 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
c0004 | 0/0 | 660 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
c0005 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
c0006 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
c0007 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 635 | 299 | 93 | 45 | 110 | 12 | 37 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
t0002 | 0/0 | 633 | 54 | 2 | 23 | 20 | 2 | 7 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
t0003 | 0/0 | 635 | 10 | 0 | 7 | 0 | 2 | 1 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
t0004 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
t0005 | 0/0 | 635 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
t0006 | 0/0 | 635 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 31 | 1 | 4 | 24 | 0 | 2 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0002 | 0/0 | 19 | 0 | 10 | 7 | 0 | 2 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0003 | 0/0 | 12 | 2 | 2 | 7 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0004 | 0/0 | 12 | 0 | 4 | 6 | 1 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0007 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0014 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 660 | 300 | 90 | 49 | 109 | 14 | 36 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0002 | 0/0 | 660 | 60 | 2 | 25 | 21 | 2 | 10 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0002c0003 | 0/0 | 660 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0003c0005 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0004c0004 | 0/0 | 660 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0005c0006 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0006c0007 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1294 | 287 | 89 | 42 | 108 | 12 | 34 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0001t0002 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0001t0003 | 0/0 | 1294 | 9 | 0 | 6 | 0 | 2 | 1 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0001t0004 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0001t0005 | 0/0 | 1294 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0001t0006 | 0/0 | 1294 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0002t0001 | 0/0 | 1294 | 7 | 0 | 2 | 2 | 0 | 3 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0001c0002t0002 | 0/0 | 1292 | 53 | 2 | 23 | 19 | 2 | 7 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0002c0003t0001 | 0/0 | 1294 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0003c0005t0001 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0004c0004t0003 | 0/0 | 1294 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0005c0006t0001 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
a0006c0007t0001 | 0/0 | 1294 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | copy fasta | chr2 | 46575937 | 46622041 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 31 | 1 | 4 | 24 | 0 | 2 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0003 | 0/0 | 12 | 2 | 2 | 7 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0004 | 0/0 | 12 | 0 | 4 | 6 | 1 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0014 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0001g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0002 | 0/0 | 19 | 0 | 10 | 7 | 0 | 2 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0002c0003t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0003c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0004c0004t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0005c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
a0006c0007t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0049 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0179 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01074 | hp2 | a0004 | c0004 | t0003 | g0209 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01167 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02280 | hp2 | a0002 | c0003 | t0001 | g0039 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0075 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03225 | hp1 | a0005 | c0006 | t0001 | g0088 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03516 | hp2 | a0006 | c0007 | t0001 | g0143 | AFR | ESN | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0227 | SAS | STU | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0077 | AFR | ASW | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0076 | EUR | TSI | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02559 | hp1 | a0003 | c0005 | t0001 | g0135 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0222 | REF | REF | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | PIGF_chr2_46575937_46622041 | PIGF | chr2 | 46575937 | 46622041 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46612295
|
T | C | 1 | a0004 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.370A>G | p.Thr124Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 463/1294 | 370/660 | 124/219 | chr2 | 46612295 | ||
chr2:46612304
|
T | C | 1 | a0003 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.361A>G | p.Thr121Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 454/1294 | 361/660 | 121/219 | chr2 | 46612304 | ||
chr2:46612318
|
G | A | 1 | a0005 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.347C>T | p.Ala116Val | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 440/1294 | 347/660 | 116/219 | chr2 | 46612318 | ||
chr2:46614938
|
T | C | 1 | a0006 | 1 | HG03516.hp2 | missense_variant&splice_region_variant | MODERATE | c.227A>G | p.Lys76Arg | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/6 | 320/1294 | 227/660 | 76/219 | chr2 | 46614938 | ||
chr2:46614980
|
A | G | 1 | a0002 | 2 | HG01167.hp2 HG02280.hp2 |
missense_variant | MODERATE | c.185T>C | p.Val62Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/6 | 278/1294 | 185/660 | 62/219 | chr2 | 46614980 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46612338
|
T | C | 1 | a0001c0002 | 60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
synonymous_variant | LOW | c.327A>G | p.Ala109Ala | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/6 | 420/1294 | 327/660 | 109/219 | chr2 | 46612338 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46581029
|
C | T | 2 | a0001c0001t0003a0004c0004t0003 | 10 | HG00741.hp2 HG01074.hp1 HG01074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*449G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 449 | chr2 | 46581029 | |||||
chr2:46581104
|
GGA | G | 2 | a0001c0001t0002a0001c0002t0002 | 54 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*372_*373delTC | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 372 | chr2 | 46581104 | |||||
chr2:46581164
|
A | G | 1 | a0001c0001t0004 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 314 | chr2 | 46581164 | |||||
chr2:46581428
|
T | G | 1 | a0001c0001t0005 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*50A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 6/6 | 50 | chr2 | 46581428 | |||||
chr2:46617032
|
G | C | 1 | a0001c0001t0006 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/6 | 1868 | chr2 | 46617032 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46581663
|
A | G | 13 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG00323.hp1 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.547-72T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46581663 | ||||||
chr2:46581907
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-316G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46581907 | ||||||
chr2:46582102
|
T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(56): Show | 74 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.547-511A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582102 | ||||||
chr2:46582232
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-641C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582232 | ||||||
chr2:46582263
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.547-672T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582263 | ||||||
chr2:46582418
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-827A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582418 | ||||||
chr2:46582482
|
T | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(60): Show | 78 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.547-891A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582482 | ||||||
chr2:46582833
|
C | G | 1 | a0001c0001t0001g0140 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.547-1242G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582833 | ||||||
chr2:46582845
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0199 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.547-1254A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46582845 | ||||||
chr2:46583765
|
G | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0118 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.547-2174C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46583765 | ||||||
chr2:46584976
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.547-3385G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46584976 | ||||||
chr2:46585088
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.547-3497T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585088 | ||||||
chr2:46585199
|
A | G | 69 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(66): Show | 88 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.547-3608T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585199 | ||||||
chr2:46585239
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.547-3648T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585239 | ||||||
chr2:46585279
|
G | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(8): Show | 11 | HG00323.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-3688C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585279 | ||||||
chr2:46585303
|
G | GT | 3 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0208 | 5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-3713dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585303 | ||||||
chr2:46585592
|
G | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0193 | 2 | NA19076.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.547-4001C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585592 | ||||||
chr2:46585864
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.547-4273G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585864 | ||||||
chr2:46585898
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0138others(2): Show | 8 | HG00597.hp2 HG03490.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-4307G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46585898 | ||||||
chr2:46586034
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-4443T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586034 | ||||||
chr2:46586155
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.547-4564G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586155 | ||||||
chr2:46586164
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-4573G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586164 | ||||||
chr2:46586229
|
C | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0108 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.547-4638G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586229 | ||||||
chr2:46586320
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0148a0001c0001t0001g0169others(2): Show | 8 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-4729G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586320 | ||||||
chr2:46586416
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.547-4825T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586416 | ||||||
chr2:46586459
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | HG00438.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.547-4868A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586459 | ||||||
chr2:46586473
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.547-4882T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586473 | ||||||
chr2:46586929
|
C | T | 2 | a0001c0002t0002g0075a0001c0002t0002g0076 | 2 | HG02698.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.547-5338G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46586929 | ||||||
chr2:46587005
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.547-5414G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587005 | ||||||
chr2:46587240
|
C | T | 1 | a0001c0002t0002g0064 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+5235G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587240 | ||||||
chr2:46587241
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.546+5234C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587241 | ||||||
chr2:46587439
|
GA | G | 45 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0082others(42): Show | 71 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.546+5035delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587439 | ||||||
chr2:46587498
|
T | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(63): Show | 83 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.546+4977A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587498 | ||||||
chr2:46587649
|
A | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0138others(2): Show | 8 | HG00597.hp2 HG03490.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+4826T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587649 | ||||||
chr2:46587756
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.546+4719T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587756 | ||||||
chr2:46587866
|
A | C | 1 | a0001c0002t0002g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.546+4609T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46587866 | ||||||
chr2:46588085
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0099a0001c0001t0001g0105others(2): Show | 7 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+4390C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588085 | ||||||
chr2:46588156
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.546+4319C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588156 | ||||||
chr2:46588341
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+4134G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588341 | ||||||
chr2:46588452
|
G | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0224 | 4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+4023C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588452 | ||||||
chr2:46588515
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.546+3960G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588515 | ||||||
chr2:46588590
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0204others(1): Show | 7 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+3885G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588590 | ||||||
chr2:46588604
|
G | A | 1 | a0001c0002t0002g0026 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.546+3871C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588604 | ||||||
chr2:46588822
|
T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(56): Show | 74 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.546+3653A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588822 | ||||||
chr2:46588989
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.546+3486T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46588989 | ||||||
chr2:46589103
|
A | C | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+3372T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589103 | ||||||
chr2:46589319
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.546+3156C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589319 | ||||||
chr2:46589326
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0094 | 4 | HG01891.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+3149G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589326 | ||||||
chr2:46589392
|
A | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(57): Show | 75 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.546+3083T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589392 | ||||||
chr2:46589415
|
G | C | 1 | a0001c0001t0001g0222 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.546+3060C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589415 | ||||||
chr2:46589513
|
T | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0083others(9): Show | 12 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+2962A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589513 | ||||||
chr2:46589611
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.546+2864G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589611 | ||||||
chr2:46589988
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0208 | 4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+2487G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46589988 | ||||||
chr2:46590370
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.546+2105A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590370 | ||||||
chr2:46590505
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.546+1970A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590505 | ||||||
chr2:46590533
|
A | ATATGT | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.546+1941_546+1942i others(7): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590533 | ||||||
chr2:46590632
|
A | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0208 | 5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+1843T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590632 | ||||||
chr2:46590852
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0208 | 5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+1623T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590852 | ||||||
chr2:46590921
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.546+1554C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590921 | ||||||
chr2:46590946
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.546+1529A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46590946 | ||||||
chr2:46591052
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.546+1423A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591052 | ||||||
chr2:46591095
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.546+1380T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591095 | ||||||
chr2:46591199
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(50): Show | 64 | HG00140.hp1 HG00140.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.546+1276G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591199 | ||||||
chr2:46591200
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0208 | 4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1275C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591200 | ||||||
chr2:46591362
|
G | C | 1 | a0004c0004t0003g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.546+1113C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591362 | ||||||
chr2:46591393
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.546+1082A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591393 | ||||||
chr2:46591395
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.546+1080G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591395 | ||||||
chr2:46591397
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.546+1078A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591397 | ||||||
chr2:46591414
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.546+1061C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591414 | ||||||
chr2:46591447
|
C | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.546+1028G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591447 | ||||||
chr2:46591612
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0199 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.546+863A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591612 | ||||||
chr2:46591644
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+831C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591644 | ||||||
chr2:46591664
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 8 | HG00597.hp2 HG01928.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+811A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591664 | ||||||
chr2:46591811
|
G | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0199 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.546+664C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591811 | ||||||
chr2:46591841
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.546+634A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591841 | ||||||
chr2:46591853
|
C | T | 33 | a0001c0001t0002g0153a0001c0002t0001g0055a0001c0002t0001g0065others(30): Show | 57 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.546+622G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591853 | ||||||
chr2:46591876
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.546+599A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591876 | ||||||
chr2:46591882
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.546+593C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591882 | ||||||
chr2:46591911
|
C | G | 1 | a0001c0001t0003g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.546+564G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46591911 | ||||||
chr2:46592095
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0096 | 3 | HG01884.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.546+380A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46592095 | ||||||
chr2:46592291
|
C | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(61): Show | 125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.546+184G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46592291 | ||||||
chr2:46592352
|
A | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.546+123T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 5/5 | chr2 | 46592352 | ||||||
chr2:46592665
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.438-82T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592665 | ||||||
chr2:46592676
|
A | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(109): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.438-93T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592676 | ||||||
chr2:46592704
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.438-121G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592704 | ||||||
chr2:46592911
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 81 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.438-328G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46592911 | ||||||
chr2:46593085
|
A | G | 10 | a0001c0001t0001g0028a0001c0001t0001g0095a0001c0001t0001g0097others(7): Show | 11 | HG01255.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-502T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593085 | ||||||
chr2:46593097
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.438-514A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593097 | ||||||
chr2:46593134
|
C | CT | 65 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0037others(62): Show | 94 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.438-552dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593134 | ||||||
chr2:46593311
|
T | G | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0085others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.438-728A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593311 | ||||||
chr2:46593426
|
C | T | 1 | a0001c0002t0002g0030 | 2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.438-843G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593426 | ||||||
chr2:46593446
|
T | G | 1 | a0001c0001t0001g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.438-863A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593446 | ||||||
chr2:46593547
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0223 | 3 | HG02976.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.438-964G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593547 | ||||||
chr2:46593567
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-984T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593567 | ||||||
chr2:46593663
|
G | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 82 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.438-1080C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593663 | ||||||
chr2:46593664
|
T | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 82 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(79): Show |
intron_variant | MODIFIER | c.438-1081A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593664 | ||||||
chr2:46593706
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.438-1123T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593706 | ||||||
chr2:46593771
|
C | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 11 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-1188G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593771 | ||||||
chr2:46593800
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.438-1217A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593800 | ||||||
chr2:46593840
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.438-1257A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593840 | ||||||
chr2:46593847
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.438-1264G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593847 | ||||||
chr2:46593929
|
A | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 81 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.438-1346T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46593929 | ||||||
chr2:46594114
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.438-1531C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594114 | ||||||
chr2:46594156
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.438-1573T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594156 | ||||||
chr2:46594308
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-1725C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594308 | ||||||
chr2:46594438
|
GA | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 81 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.438-1856delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594438 | ||||||
chr2:46594501
|
G | A | 43 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0028others(40): Show | 51 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.438-1918C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594501 | ||||||
chr2:46594536
|
AT | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(131): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.438-1954delA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594536 | ||||||
chr2:46594536
|
ATT | A | 31 | a0001c0001t0002g0153a0001c0002t0001g0055a0001c0002t0001g0065others(28): Show | 55 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.438-1955_438-1954d others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594536 | ||||||
chr2:46594565
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0003g0032a0001c0001t0003g0171others(1): Show | 5 | HG01433.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.438-1982G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594565 | ||||||
chr2:46594604
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.438-2021G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594604 | ||||||
chr2:46594755
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.438-2172G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594755 | ||||||
chr2:46594772
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG00544.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.438-2189C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594772 | ||||||
chr2:46594840
|
G | GT | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(85): Show | 157 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.438-2258dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594840 | ||||||
chr2:46594848
|
T | TG | 7 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 8 | HG00408.hp2 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.438-2266_438-2265i others(3): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594848 | ||||||
chr2:46594848
|
T | TTG | 8 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0090others(5): Show | 11 | HG00597.hp2 HG02293.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-2266_438-2265i others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594848 | ||||||
chr2:46594849
|
T | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0137a0001c0001t0001g0224 | 5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-2266A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46594849 | ||||||
chr2:46595188
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0220 | 2 | HG01261.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.438-2605G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595188 | ||||||
chr2:46595341
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438-2758G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595341 | ||||||
chr2:46595527
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.438-2944A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595527 | ||||||
chr2:46595893
|
C | G | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(64): Show | 84 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.438-3310G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46595893 | ||||||
chr2:46596000
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.438-3417C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596000 | ||||||
chr2:46596168
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.438-3585C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596168 | ||||||
chr2:46596192
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0208 | 4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-3609C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596192 | ||||||
chr2:46596199
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.438-3616G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596199 | ||||||
chr2:46596212
|
C | CA | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 80 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(77): Show |
intron_variant | MODIFIER | c.438-3630dupT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596212 | ||||||
chr2:46596283
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.438-3700C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596283 | ||||||
chr2:46596325
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.438-3742A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596325 | ||||||
chr2:46596327
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-3744C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596327 | ||||||
chr2:46596364
|
C | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0169a0001c0001t0001g0204others(1): Show | 7 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-3781G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596364 | ||||||
chr2:46596379
|
C | T | 1 | a0001c0002t0002g0052 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.438-3796G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596379 | ||||||
chr2:46596485
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0137a0001c0001t0001g0224 | 5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-3902A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596485 | ||||||
chr2:46596527
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-3944T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596527 | ||||||
chr2:46596690
|
G | C | 1 | a0001c0002t0002g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.438-4107C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596690 | ||||||
chr2:46596853
|
G | A | 55 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 82 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.438-4270C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596853 | ||||||
chr2:46596951
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.438-4368A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596951 | ||||||
chr2:46596981
|
C | G | 1 | a0001c0001t0001g0202 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.438-4398G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46596981 | ||||||
chr2:46597079
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0207 | 3 | HG01243.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.438-4496G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597079 | ||||||
chr2:46597134
|
G | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.438-4551C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597134 | ||||||
chr2:46597239
|
T | TAAAA | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.438-4657_438-4656i others(6): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597239 | ||||||
chr2:46597419
|
G | GT | 4 | a0001c0001t0001g0025a0001c0001t0001g0104a0001c0001t0001g0208others(1): Show | 6 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.438-4837dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597419 | ||||||
chr2:46597443
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-4860G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597443 | ||||||
chr2:46597465
|
T | G | 1 | a0001c0001t0001g0216 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.438-4882A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597465 | ||||||
chr2:46597475
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.438-4892G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597475 | ||||||
chr2:46597674
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.438-5091T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597674 | ||||||
chr2:46597691
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.438-5108G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597691 | ||||||
chr2:46597704
|
G | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0137a0001c0001t0001g0224 | 5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-5121C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597704 | ||||||
chr2:46597724
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.438-5141A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597724 | ||||||
chr2:46597742
|
A | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(100): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.438-5159T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597742 | ||||||
chr2:46597808
|
G | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0138others(3): Show | 9 | HG00597.hp2 HG03490.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.438-5225C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597808 | ||||||
chr2:46597941
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0099a0001c0001t0001g0105others(2): Show | 7 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.438-5358A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46597941 | ||||||
chr2:46598029
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.438-5446A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598029 | ||||||
chr2:46598192
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0112 | 3 | HG00140.hp2 HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.438-5609G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598192 | ||||||
chr2:46598198
|
G | C | 1 | a0001c0001t0001g0022 | 3 | HG02735.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.438-5615C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598198 | ||||||
chr2:46598442
|
A | G | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(65): Show | 85 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.438-5859T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598442 | ||||||
chr2:46598529
|
A | AT | 13 | a0001c0001t0001g0046a0001c0001t0001g0148a0001c0001t0001g0157others(10): Show | 13 | HG00738.hp2 HG00741.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.438-5947dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATT | 47 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0041others(44): Show | 74 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.438-5948_438-5947d others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTT | 7 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0089others(4): Show | 9 | HG01106.hp2 HG01884.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-5949_438-5947d others(5): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(4): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02818.hp1 HG02970.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-5957_438-5947d others(13): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(5): Show |
17 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0045others(14): Show | 21 | HG00140.hp2 HG01192.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.438-5958_438-5947d others(14): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(6): Show |
14 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0044others(11): Show | 18 | HG00140.hp1 HG01099.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.438-5959_438-5947d others(15): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(7): Show |
10 | a0001c0001t0001g0027a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 11 | HG01884.hp2 HG01891.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-5960_438-5947d others(16): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0107others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-5961_438-5947d others(17): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(14): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0122 | 4 | HG02615.hp2 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-5967_438-5947d others(23): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0121 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.438-5968_438-5947d others(24): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.438-5947_438-5946i others(30): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598529
|
ATTTTTTT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0094others(2): Show | 9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-5953_438-5947d others(9): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598529 | ||||||
chr2:46598569
|
G | GT | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0094others(2): Show | 9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-5987dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598569 | ||||||
chr2:46598683
|
G | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(63): Show | 83 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.438-6100C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598683 | ||||||
chr2:46598831
|
A | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(63): Show | 83 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.438-6248T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598831 | ||||||
chr2:46598844
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.438-6261A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598844 | ||||||
chr2:46598887
|
A | C | 57 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(54): Show | 84 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.438-6304T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598887 | ||||||
chr2:46598920
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0137a0001c0001t0001g0224 | 5 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.438-6337C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598920 | ||||||
chr2:46598999
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0090a0001c0001t0001g0138others(3): Show | 9 | HG00597.hp2 HG03490.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.438-6416G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46598999 | ||||||
chr2:46599242
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.438-6659T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599242 | ||||||
chr2:46599328
|
G | T | 1 | a0001c0001t0004g0084 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438-6745C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599328 | ||||||
chr2:46599432
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0144a0001c0001t0001g0208 | 5 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.438-6849G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599432 | ||||||
chr2:46599434
|
T | C | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG00323.hp1 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.438-6851A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599434 | ||||||
chr2:46599468
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0094others(2): Show | 9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-6885A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599468 | ||||||
chr2:46599657
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438-7074C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599657 | ||||||
chr2:46599750
|
T | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0199 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.438-7167A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599750 | ||||||
chr2:46599899
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.438-7316G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599899 | ||||||
chr2:46599936
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.438-7353A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599936 | ||||||
chr2:46599979
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0208 | 4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.438-7396A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46599979 | ||||||
chr2:46600160
|
C | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0028others(27): Show | 38 | HG00140.hp2 HG01099.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.438-7577G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600160 | ||||||
chr2:46600236
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.438-7653C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600236 | ||||||
chr2:46600354
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0005g0179 | 2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.438-7771T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600354 | ||||||
chr2:46600479
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0137 | 4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-7896A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600479 | ||||||
chr2:46600561
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.438-7978T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600561 | ||||||
chr2:46600576
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-7993G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600576 | ||||||
chr2:46600755
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.438-8172A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600755 | ||||||
chr2:46600841
|
C | T | 1 | a0004c0004t0003g0209 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.438-8258G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600841 | ||||||
chr2:46600938
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438-8355G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46600938 | ||||||
chr2:46601038
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.438-8455G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601038 | ||||||
chr2:46601500
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.438-8917C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601500 | ||||||
chr2:46601655
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.438-9072G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601655 | ||||||
chr2:46601952
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.438-9369T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601952 | ||||||
chr2:46601985
|
G | A | 54 | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0043others(51): Show | 81 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.438-9402C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601985 | ||||||
chr2:46601992
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.438-9409A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46601992 | ||||||
chr2:46602036
|
GA | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 80 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.438-9454delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602036 | ||||||
chr2:46602060
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438-9477T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602060 | ||||||
chr2:46602284
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.438-9701A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602284 | ||||||
chr2:46602348
|
T | G | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.438-9765A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602348 | ||||||
chr2:46602416
|
A | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+9812T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602416 | ||||||
chr2:46602679
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437+9549C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602679 | ||||||
chr2:46602790
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.437+9438C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46602790 | ||||||
chr2:46603032
|
A | G | 1 | a0001c0002t0002g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.437+9196T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603032 | ||||||
chr2:46603045
|
A | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00738.hp2 HG00741.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+9183T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603045 | ||||||
chr2:46603370
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0208 | 4 | HG00642.hp1 HG01515.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.437+8858A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603370 | ||||||
chr2:46603500
|
T | TA | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.437+8727dupT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603500 | ||||||
chr2:46603501
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.437+8727T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603501 | ||||||
chr2:46603519
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+8709G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603519 | ||||||
chr2:46603522
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.437+8706A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603522 | ||||||
chr2:46603655
|
C | T | 34 | a0001c0001t0002g0153a0001c0002t0001g0065a0001c0002t0001g0066others(31): Show | 58 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.437+8573G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603655 | ||||||
chr2:46603721
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.437+8507C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603721 | ||||||
chr2:46603923
|
C | A | 36 | a0001c0001t0002g0153a0001c0002t0001g0055a0001c0002t0001g0065others(33): Show | 60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+8305G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46603923 | ||||||
chr2:46604021
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+8207G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604021 | ||||||
chr2:46604339
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.437+7889G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604339 | ||||||
chr2:46604346
|
A | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.437+7882T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604346 | ||||||
chr2:46604361
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0097a0006c0007t0001g0143 | 3 | HG02451.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.437+7867G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604361 | ||||||
chr2:46604414
|
T | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 80 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.437+7814A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604414 | ||||||
chr2:46604855
|
G | A | 1 | a0001c0001t0001g0037 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.437+7373C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604855 | ||||||
chr2:46604927
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.437+7301A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46604927 | ||||||
chr2:46605121
|
G | T | 1 | a0001c0001t0003g0166 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.437+7107C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605121 | ||||||
chr2:46605301
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.437+6927C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605301 | ||||||
chr2:46605384
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0137 | 4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+6844A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605384 | ||||||
chr2:46605463
|
C | T | 126 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(123): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.437+6765G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605463 | ||||||
chr2:46605581
|
G | A | 1 | a0001c0001t0001g0022 | 3 | HG02735.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.437+6647C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605581 | ||||||
chr2:46605745
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.437+6483G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605745 | ||||||
chr2:46605808
|
G | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0094others(2): Show | 9 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.437+6420C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46605808 | ||||||
chr2:46606011
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.437+6217T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606011 | ||||||
chr2:46606129
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0210 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.437+6099C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606129 | ||||||
chr2:46606614
|
A | C | 4 | a0001c0001t0001g0173a0001c0001t0003g0032a0001c0001t0003g0171others(1): Show | 5 | HG01433.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+5614T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606614 | ||||||
chr2:46606701
|
T | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 80 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.437+5527A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606701 | ||||||
chr2:46606897
|
C | G | 36 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0002g0153others(33): Show | 60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+5331G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46606897 | ||||||
chr2:46607014
|
A | G | 1 | a0001c0001t0001g0033 | 2 | HG00639.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.437+5214T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607014 | ||||||
chr2:46607071
|
A | G | 2 | a0001c0002t0002g0021a0001c0002t0002g0030 | 5 | HG02071.hp1 NA18965.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+5157T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607071 | ||||||
chr2:46607074
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0204a0001c0001t0001g0213 | 3 | HG02630.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.437+5154A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607074 | ||||||
chr2:46607090
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(64): Show | 84 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.437+5138C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607090 | ||||||
chr2:46607099
|
T | C | 1 | a0001c0002t0002g0026 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.437+5129A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607099 | ||||||
chr2:46607126
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0137 | 4 | HG01081.hp2 HG02723.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+5102G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607126 | ||||||
chr2:46607163
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0094 | 4 | HG01891.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+5065A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607163 | ||||||
chr2:46607209
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+5019G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607209 | ||||||
chr2:46607310
|
A | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0096 | 3 | HG01884.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.437+4918T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607310 | ||||||
chr2:46607494
|
C | T | 1 | a0001c0002t0002g0058 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.437+4734G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607494 | ||||||
chr2:46607505
|
T | G | 1 | a0001c0001t0006g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.437+4723A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607505 | ||||||
chr2:46607533
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.437+4695A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607533 | ||||||
chr2:46607655
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437+4573A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607655 | ||||||
chr2:46607737
|
C | G | 2 | a0001c0002t0002g0056a0001c0002t0002g0057 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.437+4491G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607737 | ||||||
chr2:46607826
|
C | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+4402G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46607826 | ||||||
chr2:46608021
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.437+4207A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608021 | ||||||
chr2:46608035
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.437+4193C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608035 | ||||||
chr2:46608140
|
C | A | 1 | a0001c0002t0002g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.437+4088G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608140 | ||||||
chr2:46608243
|
G | A | 1 | a0001c0002t0002g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.437+3985C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608243 | ||||||
chr2:46608328
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.437+3900T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608328 | ||||||
chr2:46608363
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.437+3865G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608363 | ||||||
chr2:46608497
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0003g0032a0001c0001t0003g0171others(1): Show | 5 | HG01433.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.437+3731G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608497 | ||||||
chr2:46608613
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437+3615T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608613 | ||||||
chr2:46608830
|
T | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.437+3398A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608830 | ||||||
chr2:46608858
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.437+3370T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608858 | ||||||
chr2:46608860
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.437+3368A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608860 | ||||||
chr2:46608888
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0224 | 2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.437+3340T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46608888 | ||||||
chr2:46609077
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+3151C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609077 | ||||||
chr2:46609109
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0047 | 5 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+3119T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609109 | ||||||
chr2:46609136
|
G | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 8 | HG00642.hp2 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.437+3092C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609136 | ||||||
chr2:46609153
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+3075C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609153 | ||||||
chr2:46609162
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.437+3066A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609162 | ||||||
chr2:46609207
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.437+3021G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609207 | ||||||
chr2:46609208
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.437+3020C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609208 | ||||||
chr2:46609272
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.437+2956A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609272 | ||||||
chr2:46609275
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437+2953G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609275 | ||||||
chr2:46609300
|
A | T | 123 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.437+2928T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609300 | ||||||
chr2:46609363
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+2865A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609363 | ||||||
chr2:46609403
|
A | T | 36 | a0001c0002t0001g0055a0001c0002t0001g0065a0001c0002t0001g0066others(33): Show | 60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.437+2825T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609403 | ||||||
chr2:46609449
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.437+2779A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609449 | ||||||
chr2:46609614
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.437+2614G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609614 | ||||||
chr2:46609629
|
G | A | 1 | a0006c0007t0001g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.437+2599C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609629 | ||||||
chr2:46609737
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.437+2491C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609737 | ||||||
chr2:46609767
|
A | G | 57 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(54): Show | 84 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.437+2461T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609767 | ||||||
chr2:46609903
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.437+2325A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609903 | ||||||
chr2:46609936
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(60): Show | 78 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.437+2292G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609936 | ||||||
chr2:46609939
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(61): Show | 79 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(76): Show |
intron_variant | MODIFIER | c.437+2289G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46609939 | ||||||
chr2:46610361
|
C | T | 1 | a0001c0002t0002g0030 | 2 | NA18965.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.437+1867G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610361 | ||||||
chr2:46610371
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.437+1857A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610371 | ||||||
chr2:46610480
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437+1748A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610480 | ||||||
chr2:46610518
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.437+1710T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610518 | ||||||
chr2:46610526
|
C | CT | 57 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0041others(54): Show | 89 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.437+1701dupA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610526 | ||||||
chr2:46610526
|
C | CTT | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(63): Show | 81 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.437+1700_437+1701d others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610526 | ||||||
chr2:46610543
|
T | TC | 3 | a0001c0002t0002g0075a0001c0002t0002g0076a0001c0002t0002g0077 | 3 | HG02698.hp1 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.437+1684_437+1685i others(3): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610543 | ||||||
chr2:46610619
|
T | G | 1 | a0001c0001t0001g0023 | 3 | NA18957.hp2 NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.437+1609A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610619 | ||||||
chr2:46610620
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.437+1608G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610620 | ||||||
chr2:46610710
|
A | G | 29 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(26): Show | 70 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.437+1518T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610710 | ||||||
chr2:46610744
|
G | A | 1 | a0001c0001t0001g0006 | 5 | HG02056.hp1 NA18943.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.437+1484C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610744 | ||||||
chr2:46610776
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0094 | 4 | HG01891.hp1 HG02257.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+1452G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610776 | ||||||
chr2:46610839
|
C | G | 1 | a0001c0001t0001g0010 | 4 | NA18956.hp2 NA19003.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+1389G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610839 | ||||||
chr2:46610866
|
T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(51): Show | 65 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.437+1362A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610866 | ||||||
chr2:46610963
|
C | T | 1 | a0001c0002t0002g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.437+1265G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610963 | ||||||
chr2:46610990
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.437+1238C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610990 | ||||||
chr2:46610991
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.437+1237G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46610991 | ||||||
chr2:46611071
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+1157T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611071 | ||||||
chr2:46611108
|
C | G | 124 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(121): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.437+1120G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611108 | ||||||
chr2:46611183
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.437+1045A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611183 | ||||||
chr2:46611278
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.437+950C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611278 | ||||||
chr2:46611291
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0089 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.437+937G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611291 | ||||||
chr2:46611367
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.437+861G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611367 | ||||||
chr2:46611433
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.437+795C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611433 | ||||||
chr2:46611462
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0206 | 3 | HG03704.hp2 HG03927.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.437+766C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611462 | ||||||
chr2:46611469
|
C | A | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(57): Show | 75 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.437+759G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611469 | ||||||
chr2:46611470
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.437+758C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611470 | ||||||
chr2:46611482
|
C | CA | 53 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080others(50): Show | 80 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.437+745dupT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611482 | ||||||
chr2:46611517
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.437+711C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611517 | ||||||
chr2:46611719
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.437+509G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611719 | ||||||
chr2:46611720
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.437+508C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611720 | ||||||
chr2:46611793
|
T | A | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.437+435A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611793 | ||||||
chr2:46611819
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.437+409C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611819 | ||||||
chr2:46611962
|
CT | C | 50 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(47): Show | 74 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.437+265delA | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46611962 | ||||||
chr2:46612069
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.437+159A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 4/5 | chr2 | 46612069 | ||||||
chr2:46612348
|
GA | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 9 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.321-5delT | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612348 | ||||||
chr2:46612542
|
C | T | 36 | a0001c0002t0001g0055a0001c0002t0001g0065a0001c0002t0001g0066others(33): Show | 60 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.321-198G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612542 | ||||||
chr2:46612642
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.321-298A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612642 | ||||||
chr2:46612660
|
GTC | G | 56 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0042others(53): Show | 83 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.321-318_321-317del others(2): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612660 | ||||||
chr2:46612811
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.321-467C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612811 | ||||||
chr2:46612874
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.321-530A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612874 | ||||||
chr2:46612896
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.321-552A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612896 | ||||||
chr2:46612905
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0140 | 5 | NA18942.hp1 NA18953.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.321-561G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46612905 | ||||||
chr2:46613043
|
A | AAT | 13 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0079others(10): Show | 13 | HG00323.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.320+649_320+650dup others(2): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | ||||||
chr2:46613043
|
A | AATAT | 6 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 9 | HG00597.hp2 HG02040.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+647_320+650dup others(4): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | ||||||
chr2:46613043
|
A | AATATAT | 33 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0002t0001g0055others(30): Show | 57 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.320+645_320+650dup others(6): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | ||||||
chr2:46613043
|
A | AATATATA others(1): Show |
3 | a0001c0002t0002g0051a0001c0002t0002g0052a0001c0002t0002g0053 | 3 | HG02683.hp1 HG02738.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.320+643_320+650dup others(8): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | ||||||
chr2:46613043
|
A | AATATATA others(3): Show |
1 | a0001c0002t0002g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.320+641_320+650dup others(10): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613043 | ||||||
chr2:46613055
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.320+639A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613055 | ||||||
chr2:46613090
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.320+604C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613090 | ||||||
chr2:46613182
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.320+512A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613182 | ||||||
chr2:46613413
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 7 | HG00597.hp2 NA18942.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+281A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613413 | ||||||
chr2:46613541
|
T | A | 56 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0079others(53): Show | 83 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.320+153A>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613541 | ||||||
chr2:46613589
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0047 | 5 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+105A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613589 | ||||||
chr2:46613596
|
T | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(57): Show | 75 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.320+98A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 3/5 | chr2 | 46613596 | ||||||
chr2:46613956
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.229-171G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46613956 | ||||||
chr2:46613997
|
C | T | 1 | a0001c0001t0001g0018 | 3 | HG01081.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.229-212G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46613997 | ||||||
chr2:46614017
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-232C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614017 | ||||||
chr2:46614022
|
A | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(60): Show | 78 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(75): Show |
intron_variant | MODIFIER | c.229-237T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614022 | ||||||
chr2:46614058
|
A | G | 1 | a0001c0002t0002g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.229-273T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614058 | ||||||
chr2:46614305
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.229-520T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614305 | ||||||
chr2:46614339
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-554T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614339 | ||||||
chr2:46614445
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0090others(3): Show | 9 | HG00597.hp2 HG02572.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+492C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614445 | ||||||
chr2:46614505
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0141others(1): Show | 8 | HG01175.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.228+432C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614505 | ||||||
chr2:46614715
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.228+222G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614715 | ||||||
chr2:46614722
|
G | T | 48 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(45): Show | 72 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.228+215C>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614722 | ||||||
chr2:46614756
|
A | T | 1 | a0001c0002t0002g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.228+181T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 2/5 | chr2 | 46614756 | ||||||
chr2:46615271
|
A | G | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-21-86T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615271 | ||||||
chr2:46615324
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-139G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615324 | ||||||
chr2:46615417
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-21-232A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615417 | ||||||
chr2:46615586
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-21-401A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615586 | ||||||
chr2:46615864
|
G | A | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | NA18982.hp2 NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-21-679C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615864 | ||||||
chr2:46615914
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-729G>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615914 | ||||||
chr2:46615932
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-21-747C>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615932 | ||||||
chr2:46615950
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-765A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615950 | ||||||
chr2:46615959
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-21-774A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615959 | ||||||
chr2:46615968
|
C | G | 1 | a0001c0002t0002g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-21-783G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46615968 | ||||||
chr2:46616049
|
ACG | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-21-866_-21-865del others(2): Show |
PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616049 | ||||||
chr2:46616102
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-22+868C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616102 | ||||||
chr2:46616259
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-22+711A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616259 | ||||||
chr2:46616325
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-22+645A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616325 | ||||||
chr2:46616367
|
A | T | 1 | a0001c0001t0001g0022 | 3 | HG02735.hp2 HG03669.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22+603T>A | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616367 | ||||||
chr2:46616411
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22+559A>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616411 | ||||||
chr2:46616440
|
T | C | 2 | a0001c0002t0002g0021a0001c0002t0002g0030 | 5 | HG02071.hp1 NA18965.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+530A>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616440 | ||||||
chr2:46616467
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-22+503G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616467 | ||||||
chr2:46616492
|
A | G | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-22+478T>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616492 | ||||||
chr2:46616526
|
C | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0218a0001c0001t0001g0219others(5): Show | 10 | HG00735.hp2 HG01167.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+444G>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616526 | ||||||
chr2:46616617
|
A | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-22+353T>G | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616617 | ||||||
chr2:46616676
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22+294C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616676 | ||||||
chr2:46616781
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-22+189G>C | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616781 | ||||||
chr2:46616919
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-22+51C>T | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616919 | ||||||
chr2:46616943
|
A | AG | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-22+26_-22+27insC | PIGF | ENSG00000151665.13 | transcript | ENST00000281382.11 | protein_coding | 1/5 | chr2 | 46616943 |