geneid | 11137 |
---|---|
ensemblid | ENSG00000136045.12 |
hgncid | 17015 |
symbol | PWP1 |
name | PWP1 homolog, endonuclein |
refseq_nuc | NM_007062.3 |
refseq_prot | NP_008993.1 |
ensembl_nuc | ENST00000412830.8 |
ensembl_prot | ENSP00000387365.3 |
mane_status | MANE Select |
chr | chr12 |
start | 107685799 |
end | 107713162 |
strand | + |
ver | v1.2 |
region | chr12:107685799-107713162 |
region5000 | chr12:107680799-107718162 |
regionname0 | PWP1_chr12_107685799_107713162 |
regionname5000 | PWP1_chr12_107680799_107718162 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 501 | 299 | 78 | 60 | 110 | 13 | 36 | 84 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0002 | 0/0 | 501 | 24 | 2 | 2 | 15 | 1 | 4 | 12 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0003 | 0/0 | 501 | 12 | 0 | 0 | 11 | 0 | 1 | 10 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0004 | 0/0 | 501 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0005 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0006 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0007 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0008 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0009 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1506 | 277 | 57 | 59 | 110 | 13 | 36 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0002 | 0/0 | 1506 | 24 | 2 | 2 | 15 | 1 | 4 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0003 | 0/0 | 1506 | 18 | 17 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0004 | 0/0 | 1506 | 12 | 0 | 0 | 11 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0005 | 0/0 | 1506 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0006 | 0/0 | 1506 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0007 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0008 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0009 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0010 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
c0011 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1044 | 163 | 20 | 37 | 79 | 8 | 19 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0002 | 1/1 | 1044 | 152 | 45 | 25 | 53 | 5 | 22 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0003 | 0/0 | 1044 | 8 | 7 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0004 | 0/0 | 1044 | 5 | 5 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0005 | 0/0 | 1044 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0006 | 0/0 | 1044 | 3 | 0 | 0 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0007 | 0/0 | 1044 | 2 | 0 | 1 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0008 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0009 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0010 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0011 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
t0012 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 0 | 8 | 7 | 1 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0002 | 0/0 | 11 | 0 | 5 | 3 | 0 | 3 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0003 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0005 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0006 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1506 | 277 | 57 | 59 | 110 | 13 | 36 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0003 | 0/0 | 1506 | 18 | 17 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0005 | 0/0 | 1506 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0002c0002 | 0/0 | 1506 | 24 | 2 | 2 | 15 | 1 | 4 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0003c0004 | 0/0 | 1506 | 12 | 0 | 0 | 11 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0004c0006 | 0/0 | 1506 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0005c0011 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0006c0007 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0007c0010 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0008c0008 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0009c0009 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2549 | 144 | 3 | 36 | 79 | 8 | 18 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0002 | 1/1 | 2549 | 111 | 39 | 22 | 27 | 4 | 17 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0003 | 0/0 | 2549 | 8 | 7 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0004 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0005 | 0/0 | 2549 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0006 | 0/0 | 2549 | 3 | 0 | 0 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0007 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0008 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0009 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0010 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0011 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0001t0012 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0003t0001 | 0/0 | 2549 | 18 | 17 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0001c0005t0004 | 0/0 | 2549 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0002c0002t0002 | 0/0 | 2549 | 24 | 2 | 2 | 15 | 1 | 4 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0003c0004t0002 | 0/0 | 2549 | 12 | 0 | 0 | 11 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0004c0006t0002 | 0/0 | 2549 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0005c0011t0007 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0006c0007t0002 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0007c0010t0002 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0008c0008t0002 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
a0009c0009t0001 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | copy fasta | chr12 | 107680799 | 107718162 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 8 | 7 | 1 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0002 | 0/0 | 11 | 0 | 5 | 3 | 0 | 3 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0008g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0010g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0005t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0005t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0001c0005t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0003c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0004c0006t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0004c0006t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0005c0011t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0006c0007t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0007c0010t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0008c0008t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
a0009c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0029 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0063 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | FIN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00642 | hp1 | a0005 | c0011 | t0007 | g0185 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0137 | AMR | PUR | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01261 | hp2 | a0008 | c0008 | t0002 | g0161 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0181 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02027 | hp1 | a0003 | c0004 | t0002 | g0049 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | CDX | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02293 | hp1 | a0001 | c0001 | t0010 | g0110 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02602 | hp2 | a0003 | c0004 | t0002 | g0053 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0130 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0131 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02647 | hp1 | a0001 | c0005 | t0004 | g0045 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0128 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0189 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02896 | hp1 | a0004 | c0006 | t0002 | g0239 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02897 | hp2 | a0004 | c0006 | t0002 | g0238 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0180 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03098 | hp1 | a0001 | c0005 | t0004 | g0044 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03098 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03453 | hp1 | a0007 | c0010 | t0002 | g0043 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03486 | hp1 | a0001 | c0005 | t0004 | g0017 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0183 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0176 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0172 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03942 | hp1 | a0009 | c0009 | t0001 | g0105 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | STU | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18906 | hp2 | a0001 | c0005 | t0004 | g0017 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18954 | hp1 | a0003 | c0004 | t0002 | g0051 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18964 | hp1 | a0003 | c0004 | t0002 | g0048 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18983 | hp2 | a0003 | c0004 | t0002 | g0050 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18994 | hp2 | a0003 | c0004 | t0002 | g0046 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19004 | hp1 | a0003 | c0004 | t0002 | g0018 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19043 | hp2 | a0006 | c0007 | t0002 | g0086 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19055 | hp2 | a0003 | c0004 | t0002 | g0047 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19063 | hp2 | a0001 | c0001 | t0008 | g0108 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19065 | hp2 | a0003 | c0004 | t0002 | g0018 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19068 | hp2 | a0003 | c0004 | t0002 | g0019 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19081 | hp1 | a0003 | c0004 | t0002 | g0052 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ASW | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ASW | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | TSI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0139 | AFR | ACB | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA18955 | hp2 | a0003 | c0004 | t0002 | g0019 | EAS | JPT | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0072 | AFR | LWK | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0078 | REF | REF | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0021 | REF | REF | PWP1_chr12_107680799_107718162 | PWP1 | chr12 | 107680799 | 107718162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107688476
|
G | A | 1 | a0003 | 12 | HG02027.hp1 HG02602.hp2 NA18954.hp1 others(9): Show |
missense_variant | MODERATE | c.101G>A | p.Arg34His | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 2/15 | 202/2549 | 101/1506 | 34/501 | chr12 | 107688476 | ||
chr12:107688682
|
C | T | 1 | a0005 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.199C>T | p.Arg67Cys | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/15 | 300/2549 | 199/1506 | 67/501 | chr12 | 107688682 | ||
chr12:107688737
|
G | A | 1 | a0006 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.254G>A | p.Arg85Lys | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/15 | 355/2549 | 254/1506 | 85/501 | chr12 | 107688737 | ||
chr12:107688797
|
A | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.314A>G | p.Asp105Gly | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/15 | 415/2549 | 314/1506 | 105/501 | chr12 | 107688797 | ||
chr12:107696490
|
A | C | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.519A>C | p.Glu173Asp | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/15 | 620/2549 | 519/1506 | 173/501 | chr12 | 107696490 | ||
chr12:107702992
|
G | C | 1 | a0002 | 24 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(21): Show |
missense_variant | MODERATE | c.864G>C | p.Leu288Phe | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/15 | 965/2549 | 864/1506 | 288/501 | chr12 | 107702992 | ||
chr12:107708980
|
A | G | 1 | a0009 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1132A>G | p.Ile378Val | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 12/15 | 1233/2549 | 1132/1506 | 378/501 | chr12 | 107708980 | ||
chr12:107712116
|
G | A | 1 | a0008 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1402G>A | p.Glu468Lys | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 1503/2549 | 1402/1506 | 468/501 | chr12 | 107712116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107692857
|
C | T | 1 | a0001c0005 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.363C>T | p.Tyr121Tyr | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 4/15 | 464/2549 | 363/1506 | 121/501 | chr12 | 107692857 | ||
chr12:107702941
|
T | C | 1 | a0001c0003 | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
synonymous_variant | LOW | c.813T>C | p.Val271Val | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/15 | 914/2549 | 813/1506 | 271/501 | chr12 | 107702941 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107685811
|
C | T | 1 | a0001c0001t0012 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/15 | 89 | chr12 | 107685811 | |||||
chr12:107685856
|
A | G | 1 | a0001c0001t0011 | 1 | HG02717.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/15 | chr12 | 107685856 | ||||||
chr12:107712227
|
T | G | 1 | a0001c0001t0008 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 7 | chr12 | 107712227 | |||||
chr12:107712281
|
T | C | 4 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(1): Show | 11 | HG00642.hp1 HG01516.hp1 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*61T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 61 | chr12 | 107712281 | |||||
chr12:107712378
|
G | A | 1 | a0001c0001t0005 | 4 | HG02622.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 158 | chr12 | 107712378 | |||||
chr12:107712480
|
T | C | 2 | a0001c0001t0004a0001c0005t0004 | 5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*260T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 260 | chr12 | 107712480 | |||||
chr12:107712542
|
G | A | 1 | a0001c0001t0010 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 322 | chr12 | 107712542 | |||||
chr12:107712630
|
G | C | 2 | a0001c0001t0007a0005c0011t0007 | 2 | HG00642.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 410 | chr12 | 107712630 | |||||
chr12:107712647
|
C | T | 1 | a0001c0001t0006 | 3 | HG02155.hp1 NA18972.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*427C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 427 | chr12 | 107712647 | |||||
chr12:107712771
|
T | C | 2 | a0001c0001t0004a0001c0005t0004 | 5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*551T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 551 | chr12 | 107712771 | |||||
chr12:107713045
|
G | A | 1 | a0001c0001t0009 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 825 | chr12 | 107713045 | |||||
chr12:107713138
|
T | C | 9 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(6): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*918T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 15/15 | 918 | chr12 | 107713138 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:107686044
|
C | A | 1 | a0001c0005t0004g0017 | 2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72+73C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686044 | ||||||
chr12:107686089
|
T | G | 1 | a0007c0010t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+118T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686089 | ||||||
chr12:107686116
|
G | T | 2 | a0001c0001t0005g0016a0001c0001t0005g0242 | 4 | HG02622.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+145G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686116 | ||||||
chr12:107686193
|
C | A | 1 | a0001c0005t0004g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.72+222C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686193 | ||||||
chr12:107686200
|
C | T | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(94): Show | 133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.72+229C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686200 | ||||||
chr12:107686205
|
C | A | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+234C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686205 | ||||||
chr12:107686255
|
G | T | 1 | a0001c0001t0002g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.72+284G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686255 | ||||||
chr12:107686486
|
T | A | 10 | a0003c0004t0002g0018a0003c0004t0002g0019a0003c0004t0002g0046others(7): Show | 12 | HG02027.hp1 HG02602.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+515T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686486 | ||||||
chr12:107686502
|
A | T | 25 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(22): Show | 42 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.72+531A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686502 | ||||||
chr12:107686662
|
C | T | 2 | a0001c0001t0002g0240a0001c0001t0002g0241 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72+691C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686662 | ||||||
chr12:107686735
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.72+764G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686735 | ||||||
chr12:107686760
|
A | G | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.72+789A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686760 | ||||||
chr12:107686767
|
G | C | 1 | a0001c0001t0006g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.72+796G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686767 | ||||||
chr12:107686773
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72+802T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686773 | ||||||
chr12:107686811
|
AAAAAATT others(1058): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.72+851_73-562del | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686811 | |||||
chr12:107686834
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+863T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686834 | ||||||
chr12:107686837
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+866A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686837 | ||||||
chr12:107686838
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+867T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107686838 | ||||||
chr12:107686969
|
CA | C | 51 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(48): Show | 76 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.72+1029delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | |||||
chr12:107686969
|
CAA | C | 7 | a0001c0001t0002g0011a0001c0001t0002g0094a0001c0001t0002g0095others(4): Show | 9 | HG00558.hp1 HG01167.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+1028_72+1029del others(2): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | |||||
chr12:107686969
|
CAAA | C | 3 | a0001c0001t0005g0016a0001c0001t0005g0242a0001c0005t0004g0017 | 6 | HG02622.hp1 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+1027_72+1029del others(3): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | |||||
chr12:107686969
|
CAAAAA | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0098others(4): Show | 9 | HG01109.hp2 HG01167.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+1025_72+1029del others(5): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | |||||
chr12:107686969
|
CAAAAAA | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(25): Show | 52 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.72+1024_72+1029del others(6): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | |||||
chr12:107686969
|
CAAAAAAA others(13): Show |
C | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(112): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.72+1010_72+1029del others(20): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107686969 | |||||
chr12:107687101
|
C | T | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+1130C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687101 | ||||||
chr12:107687402
|
C | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(59): Show | 88 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.73-1046C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687402 | ||||||
chr12:107687440
|
C | T | 36 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(33): Show | 47 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-1008C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687440 | ||||||
chr12:107687629
|
G | A | 9 | a0003c0004t0002g0018a0003c0004t0002g0019a0003c0004t0002g0046others(6): Show | 11 | HG02027.hp1 NA18954.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-819G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687629 | ||||||
chr12:107687705
|
G | T | 1 | a0001c0001t0001g0237 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.73-743G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687705 | ||||||
chr12:107687840
|
C | T | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(99): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.73-608C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687840 | ||||||
chr12:107687979
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.73-469C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687979 | ||||||
chr12:107687983
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.73-465A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107687983 | ||||||
chr12:107688005
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.73-443T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688005 | ||||||
chr12:107688030
|
C | CA | 14 | a0001c0001t0001g0103a0001c0001t0002g0031a0001c0001t0002g0056others(11): Show | 15 | HG00423.hp1 HG01358.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.73-388dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA | 5 | a0001c0001t0001g0042a0001c0001t0001g0233a0001c0001t0006g0164others(2): Show | 6 | HG01243.hp2 HG01515.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-394_73-388dupAA others(5): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(1): Show |
22 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 33 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-395_73-388dupAA others(6): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0038others(20): Show | 34 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-396_73-388dupAA others(7): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(3): Show |
14 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0127others(11): Show | 17 | HG00438.hp1 HG01433.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.73-397_73-388dupAA others(8): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 5 | HG01123.hp1 HG01978.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-398_73-388dupAA others(9): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0196 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.73-403_73-388dupAA others(14): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0195 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-404_73-388dupAA others(15): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0194 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.73-405_73-388dupAA others(16): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
CA | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(66): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-388delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
CAA | C | 9 | a0001c0001t0001g0071a0001c0001t0001g0102a0001c0001t0001g0122others(6): Show | 9 | HG01515.hp1 HG02976.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-389_73-388delAA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-397_73-388delAA others(8): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0236 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.73-400_73-388delAA others(11): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.73-401_73-388delAA others(12): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688030
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73-402_73-388delAA others(13): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 107688030 | |||||
chr12:107688129
|
A | G | 1 | a0001c0005t0004g0045 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-319A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688129 | ||||||
chr12:107688263
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 4 | HG01081.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-185G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688263 | ||||||
chr12:107688289
|
TC | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(60): Show | 89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.73-158delC | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688289 | ||||||
chr12:107688357
|
C | T | 1 | a0007c0010t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-91C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688357 | ||||||
chr12:107688395
|
T | A | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73-53T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 1/14 | chr12 | 107688395 | ||||||
chr12:107688838
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.319+36A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107688838 | ||||||
chr12:107689150
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.319+348C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689150 | ||||||
chr12:107689164
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.319+362C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689164 | ||||||
chr12:107689178
|
G | A | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+376G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689178 | ||||||
chr12:107689334
|
G | A | 1 | a0001c0005t0004g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.319+532G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689334 | ||||||
chr12:107689558
|
C | G | 1 | a0007c0010t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319+756C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689558 | ||||||
chr12:107689876
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(58): Show | 87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.319+1074C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689876 | ||||||
chr12:107689882
|
A | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(112): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.319+1080A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689882 | ||||||
chr12:107689904
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 4 | HG01081.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1102G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689904 | ||||||
chr12:107689915
|
G | A | 2 | a0001c0003t0001g0130a0001c0003t0001g0134 | 2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.319+1113G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689915 | ||||||
chr12:107689952
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0070a0001c0001t0002g0090others(1): Show | 5 | HG01109.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+1150C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107689952 | ||||||
chr12:107690018
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.319+1216G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690018 | ||||||
chr12:107690123
|
T | G | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+1321T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690123 | ||||||
chr12:107690341
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(35): Show | 64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.319+1539T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690341 | ||||||
chr12:107690472
|
T | G | 1 | a0001c0001t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.319+1670T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690472 | ||||||
chr12:107690506
|
C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 4 | HG01081.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1704C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690506 | ||||||
chr12:107690672
|
G | A | 1 | a0001c0001t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.319+1870G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690672 | ||||||
chr12:107690682
|
C | G | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1880C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690682 | ||||||
chr12:107690859
|
A | T | 6 | a0001c0001t0002g0089a0001c0003t0001g0030a0001c0003t0001g0129others(3): Show | 7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-1955A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690859 | ||||||
chr12:107690913
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(1): Show | 4 | NA18983.hp1 NA19063.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-1901G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690913 | ||||||
chr12:107690953
|
C | T | 1 | a0001c0001t0009g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.320-1861C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107690953 | ||||||
chr12:107691086
|
A | G | 1 | a0001c0001t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.320-1728A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691086 | ||||||
chr12:107691546
|
G | A | 1 | a0002c0002t0002g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.320-1268G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691546 | ||||||
chr12:107691601
|
A | G | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.320-1213A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691601 | ||||||
chr12:107691605
|
G | A | 2 | a0001c0001t0005g0016a0001c0001t0005g0242 | 4 | HG02622.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1209G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691605 | ||||||
chr12:107691631
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0073 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.320-1183G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691631 | ||||||
chr12:107691673
|
CTTA | C | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.320-1136_320-1134d others(5): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 107691673 | |||||
chr12:107691679
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0073 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.320-1135A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691679 | ||||||
chr12:107691746
|
T | A | 20 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(17): Show | 22 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.320-1068T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691746 | ||||||
chr12:107691793
|
G | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(118): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.320-1021G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691793 | ||||||
chr12:107691805
|
C | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0088 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.320-1009C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691805 | ||||||
chr12:107691824
|
T | C | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.320-990T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107691824 | ||||||
chr12:107692122
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0199 | 3 | NA18967.hp1 NA19064.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.320-692G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692122 | ||||||
chr12:107692213
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.320-601G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692213 | ||||||
chr12:107692217
|
C | T | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.320-597C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692217 | ||||||
chr12:107692249
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.320-565C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692249 | ||||||
chr12:107692465
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.320-349T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692465 | ||||||
chr12:107692468
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.320-346T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692468 | ||||||
chr12:107692574
|
G | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(96): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.320-240G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692574 | ||||||
chr12:107692732
|
AGTCCAAG others(7): Show |
A | 2 | a0001c0001t0002g0150a0001c0001t0002g0163 | 2 | NA18982.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.320-78_320-65delCA others(12): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 107692732 | |||||
chr12:107692770
|
A | G | 3 | a0001c0003t0001g0128a0001c0003t0001g0132a0001c0003t0001g0136 | 3 | HG02486.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.320-44A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 3/14 | chr12 | 107692770 | ||||||
chr12:107692920
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.405+21T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 4/14 | chr12 | 107692920 | ||||||
chr12:107693119
|
A | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(60): Show | 89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.502+23A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693119 | ||||||
chr12:107693185
|
T | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0058 | 3 | HG01243.hp1 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.502+89T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693185 | ||||||
chr12:107693337
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.502+241G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693337 | ||||||
chr12:107693462
|
G | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.502+366G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693462 | ||||||
chr12:107693479
|
C | G | 1 | a0001c0001t0002g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502+383C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693479 | ||||||
chr12:107693649
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.502+553C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693649 | ||||||
chr12:107693900
|
G | C | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.502+804G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693900 | ||||||
chr12:107693920
|
C | T | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.502+824C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107693920 | ||||||
chr12:107694019
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.502+923G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694019 | ||||||
chr12:107694109
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.502+1013G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694109 | ||||||
chr12:107694127
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.502+1031G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694127 | ||||||
chr12:107694195
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.502+1099T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694195 | ||||||
chr12:107694257
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0106a0001c0001t0001g0124 | 4 | HG00597.hp2 HG02698.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1161A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694257 | ||||||
chr12:107694263
|
G | A | 1 | a0007c0010t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.502+1167G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694263 | ||||||
chr12:107694294
|
G | T | 4 | a0003c0004t0002g0018a0003c0004t0002g0047a0003c0004t0002g0050others(1): Show | 5 | NA18954.hp1 NA18983.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+1198G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694294 | ||||||
chr12:107694500
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.502+1404C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694500 | ||||||
chr12:107694610
|
A | G | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1514A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694610 | ||||||
chr12:107694681
|
A | G | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+1585A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694681 | ||||||
chr12:107694905
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.503-1569A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694905 | ||||||
chr12:107694923
|
G | C | 3 | a0001c0001t0006g0164a0001c0001t0006g0211a0001c0001t0006g0223 | 3 | HG02155.hp1 NA18972.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.503-1551G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694923 | ||||||
chr12:107694938
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.503-1536G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694938 | ||||||
chr12:107694988
|
A | G | 1 | a0001c0003t0001g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.503-1486A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107694988 | ||||||
chr12:107695099
|
C | CA | 9 | a0001c0001t0001g0170a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG02056.hp1 HG02622.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-1358dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107695099 | |||||
chr12:107695099
|
CA | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(78): Show | 120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.503-1358delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107695099 | |||||
chr12:107695182
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.503-1292C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695182 | ||||||
chr12:107695244
|
C | T | 1 | a0008c0008t0002g0161 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.503-1230C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695244 | ||||||
chr12:107695265
|
C | CA | 21 | a0001c0001t0002g0151a0001c0003t0001g0030a0001c0003t0001g0128others(18): Show | 22 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.503-1197dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107695265 | |||||
chr12:107695474
|
T | C | 1 | a0001c0003t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.503-1000T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695474 | ||||||
chr12:107695556
|
G | A | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.503-918G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695556 | ||||||
chr12:107695593
|
A | G | 4 | a0001c0001t0001g0027a0001c0005t0004g0017a0001c0005t0004g0044others(1): Show | 6 | HG00280.hp1 HG00741.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-881A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695593 | ||||||
chr12:107695866
|
T | C | 2 | a0001c0001t0002g0060a0001c0001t0002g0061 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.503-608T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695866 | ||||||
chr12:107695966
|
G | T | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.503-508G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695966 | ||||||
chr12:107695986
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.503-488G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107695986 | ||||||
chr12:107696029
|
C | CT | 51 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0112others(48): Show | 65 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.503-424dupT | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107696029 | |||||
chr12:107696029
|
C | CTT | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.503-425_503-424dup others(2): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107696029 | |||||
chr12:107696029
|
C | CTTT | 15 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0119others(12): Show | 16 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.503-426_503-424dup others(3): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 107696029 | |||||
chr12:107696221
|
C | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(63): Show | 93 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.503-253C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107696221 | ||||||
chr12:107696244
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.503-230G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 5/14 | chr12 | 107696244 | ||||||
chr12:107696667
|
A | C | 1 | a0001c0001t0002g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.613+83A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696667 | ||||||
chr12:107696691
|
T | C | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.613+107T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696691 | ||||||
chr12:107696741
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.613+157A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696741 | ||||||
chr12:107696900
|
G | A | 2 | a0002c0002t0002g0176a0002c0002t0002g0180 | 2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.613+316G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696900 | ||||||
chr12:107696904
|
C | T | 2 | a0002c0002t0002g0176a0002c0002t0002g0180 | 2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.613+320C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107696904 | ||||||
chr12:107697019
|
A | C | 1 | a0001c0001t0002g0033 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.613+435A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107697019 | ||||||
chr12:107697143
|
A | G | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.614-324A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107697143 | ||||||
chr12:107697434
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.614-33G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 6/14 | chr12 | 107697434 | ||||||
chr12:107697848
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.744+251T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107697848 | ||||||
chr12:107697876
|
C | G | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.744+279C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107697876 | ||||||
chr12:107697877
|
G | A | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.744+280G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107697877 | ||||||
chr12:107698106
|
A | C | 1 | a0001c0001t0002g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.744+509A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698106 | ||||||
chr12:107698269
|
G | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.744+672G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698269 | ||||||
chr12:107698418
|
T | C | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.744+821T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698418 | ||||||
chr12:107698469
|
T | C | 1 | a0001c0003t0001g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.744+872T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698469 | ||||||
chr12:107698514
|
C | T | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.745-859C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698514 | ||||||
chr12:107698592
|
C | T | 1 | a0002c0002t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.745-781C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698592 | ||||||
chr12:107698738
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.745-635G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698738 | ||||||
chr12:107698894
|
T | C | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.745-479T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698894 | ||||||
chr12:107698914
|
G | GTCTCTAA others(28): Show |
1 | a0001c0001t0008g0108 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.745-435_745-434ins others(35): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 107698914 | |||||
chr12:107698939
|
A | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.745-434A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698939 | ||||||
chr12:107698970
|
A | C | 1 | a0001c0001t0002g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.745-403A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698970 | ||||||
chr12:107698980
|
T | C | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-393T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107698980 | ||||||
chr12:107699028
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.745-345C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107699028 | ||||||
chr12:107699219
|
A | G | 3 | a0002c0002t0002g0029a0002c0002t0002g0125a0002c0002t0002g0126 | 4 | HG00099.hp1 HG00735.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-154A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107699219 | ||||||
chr12:107699238
|
A | G | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.745-135A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 7/14 | chr12 | 107699238 | ||||||
chr12:107699505
|
C | G | 1 | a0001c0001t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.806+71C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699505 | ||||||
chr12:107699603
|
C | A | 8 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 9 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.806+169C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699603 | ||||||
chr12:107699679
|
A | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0073 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.806+245A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699679 | ||||||
chr12:107699819
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.806+385C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107699819 | ||||||
chr12:107700025
|
G | A | 1 | a0001c0001t0002g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.806+591G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700025 | ||||||
chr12:107700241
|
G | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(98): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.806+807G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700241 | ||||||
chr12:107700288
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806+854A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700288 | ||||||
chr12:107700311
|
G | A | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.806+877G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700311 | ||||||
chr12:107700450
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.806+1016A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700450 | ||||||
chr12:107700561
|
C | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(57): Show | 86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.806+1127C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700561 | ||||||
chr12:107700605
|
G | A | 1 | a0009c0009t0001g0105 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.806+1171G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700605 | ||||||
chr12:107700627
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.806+1193A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700627 | ||||||
chr12:107700882
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.806+1448G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700882 | ||||||
chr12:107700897
|
T | TC | 41 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(38): Show | 67 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.806+1470dupC | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 107700897 | |||||
chr12:107700930
|
A | G | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.806+1496A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700930 | ||||||
chr12:107700964
|
A | C | 1 | a0001c0001t0002g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.806+1530A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107700964 | ||||||
chr12:107701203
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(35): Show | 64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.807-1732T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701203 | ||||||
chr12:107701240
|
A | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.807-1695A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701240 | ||||||
chr12:107701288
|
T | G | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.807-1647T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701288 | ||||||
chr12:107701339
|
A | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.807-1596A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701339 | ||||||
chr12:107701418
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.807-1517T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701418 | ||||||
chr12:107701429
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.807-1506G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701429 | ||||||
chr12:107701496
|
T | A | 1 | a0001c0001t0002g0078 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.807-1439T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701496 | ||||||
chr12:107701534
|
C | T | 4 | a0001c0001t0002g0024a0001c0001t0002g0070a0001c0001t0002g0090others(1): Show | 5 | HG01109.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.807-1401C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701534 | ||||||
chr12:107701563
|
A | G | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.807-1372A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701563 | ||||||
chr12:107701766
|
C | T | 1 | a0006c0007t0002g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.807-1169C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701766 | ||||||
chr12:107701803
|
G | A | 1 | a0001c0003t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.807-1132G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701803 | ||||||
chr12:107701936
|
G | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.807-999G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701936 | ||||||
chr12:107701977
|
C | T | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.807-958C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107701977 | ||||||
chr12:107702177
|
T | C | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.807-758T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702177 | ||||||
chr12:107702243
|
C | CT | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(35): Show | 64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.807-683dupT | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 107702243 | |||||
chr12:107702319
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.807-616T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702319 | ||||||
chr12:107702338
|
T | C | 1 | a0001c0001t0007g0181 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.807-597T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702338 | ||||||
chr12:107702367
|
G | A | 1 | a0001c0003t0001g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.807-568G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702367 | ||||||
chr12:107702403
|
C | T | 1 | a0002c0002t0002g0173 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.807-532C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702403 | ||||||
chr12:107702614
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.807-321A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702614 | ||||||
chr12:107702755
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(38): Show | 68 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.807-180T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702755 | ||||||
chr12:107702780
|
C | T | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.807-155C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 8/14 | chr12 | 107702780 | ||||||
chr12:107703113
|
T | C | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+82T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703113 | ||||||
chr12:107703348
|
G | T | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.903+317G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703348 | ||||||
chr12:107703602
|
C | T | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.904-83C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703602 | ||||||
chr12:107703658
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109 | 3 | NA18983.hp1 NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.904-27C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703658 | ||||||
chr12:107703678
|
C | T | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.904-7C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 9/14 | chr12 | 107703678 | ||||||
chr12:107704024
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.965+278G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704024 | ||||||
chr12:107704193
|
G | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.966-443G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704193 | ||||||
chr12:107704262
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(55): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.966-374T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704262 | ||||||
chr12:107704288
|
G | C | 26 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(23): Show | 42 | HG00558.hp1 HG00597.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.966-348G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704288 | ||||||
chr12:107704339
|
T | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0224 | 2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.966-297T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 10/14 | chr12 | 107704339 | ||||||
chr12:107704810
|
G | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(57): Show | 86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1077+63G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704810 | ||||||
chr12:107704935
|
T | C | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1077+188T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704935 | ||||||
chr12:107704961
|
C | G | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077+214C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704961 | ||||||
chr12:107704974
|
G | A | 3 | a0001c0001t0002g0075a0001c0001t0002g0080a0001c0001t0002g0096 | 3 | HG01167.hp1 HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1077+227G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107704974 | ||||||
chr12:107705080
|
G | T | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1077+333G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705080 | ||||||
chr12:107705149
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1077+402G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705149 | ||||||
chr12:107705179
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1077+432T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705179 | ||||||
chr12:107705264
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(29): Show | 58 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1077+517G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705264 | ||||||
chr12:107705355
|
T | C | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077+608T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705355 | ||||||
chr12:107705361
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1077+614G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705361 | ||||||
chr12:107705388
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1077+641A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705388 | ||||||
chr12:107705505
|
T | C | 23 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0001g0121others(20): Show | 30 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1077+758T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705505 | ||||||
chr12:107705518
|
C | G | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1077+771C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705518 | ||||||
chr12:107705520
|
T | TC | 45 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0100others(42): Show | 50 | HG00597.hp1 HG00621.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1077+779dupC | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 107705520 | |||||
chr12:107705524
|
C | A | 1 | a0001c0001t0002g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1077+777C>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705524 | ||||||
chr12:107705555
|
T | A | 1 | a0001c0001t0002g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1077+808T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705555 | ||||||
chr12:107705640
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1077+893A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705640 | ||||||
chr12:107705742
|
A | C | 1 | a0001c0001t0004g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077+995A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705742 | ||||||
chr12:107705764
|
A | C | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077+1017A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705764 | ||||||
chr12:107705772
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1077+1025A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705772 | ||||||
chr12:107705846
|
CACATATG others(11): Show |
C | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(60): Show | 89 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1077+1100_1077+111 others(22): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705846 | ||||||
chr12:107705885
|
A | C | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1077+1138A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705885 | ||||||
chr12:107705930
|
G | A | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1077+1183G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107705930 | ||||||
chr12:107706050
|
C | G | 3 | a0001c0005t0004g0017a0001c0005t0004g0044a0001c0005t0004g0045 | 4 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+1303C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706050 | ||||||
chr12:107706216
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1077+1469A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706216 | ||||||
chr12:107706308
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1077+1561G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706308 | ||||||
chr12:107706382
|
G | A | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1077+1635G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706382 | ||||||
chr12:107706540
|
A | T | 5 | a0001c0003t0001g0137a0001c0003t0001g0138a0001c0003t0001g0140others(2): Show | 5 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+1793A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706540 | ||||||
chr12:107706641
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1077+1894A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706641 | ||||||
chr12:107706709
|
T | C | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(2): Show | 5 | HG00323.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+1962T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706709 | ||||||
chr12:107706844
|
C | G | 3 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0065 | 3 | HG02055.hp2 HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1078-2082C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706844 | ||||||
chr12:107706902
|
T | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0073 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1078-2024T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706902 | ||||||
chr12:107706976
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1078-1950C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706976 | ||||||
chr12:107706985
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1941T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706985 | ||||||
chr12:107706995
|
T | A | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1931T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706995 | ||||||
chr12:107706996
|
G | C | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1930G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706996 | ||||||
chr12:107706999
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1927T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107706999 | ||||||
chr12:107707000
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1926A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707000 | ||||||
chr12:107707002
|
T | G | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1924T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707002 | ||||||
chr12:107707008
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1078-1918A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707008 | ||||||
chr12:107707028
|
A | T | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1898A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707028 | ||||||
chr12:107707063
|
T | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0070a0001c0001t0002g0090others(1): Show | 5 | HG01109.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-1863T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707063 | ||||||
chr12:107707094
|
TCTC | T | 32 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0174others(29): Show | 43 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1078-1829_1078-182 others(7): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 107707094 | |||||
chr12:107707118
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0002g0182 | 2 | NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1078-1808T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707118 | ||||||
chr12:107707126
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1078-1800A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707126 | ||||||
chr12:107707162
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1764A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707162 | ||||||
chr12:107707163
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1763T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707163 | ||||||
chr12:107707194
|
G | C | 1 | a0001c0001t0002g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1732G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707194 | ||||||
chr12:107707196
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-1730T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707196 | ||||||
chr12:107707352
|
T | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(37): Show | 67 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-1574T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707352 | ||||||
chr12:107707413
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1078-1513G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707413 | ||||||
chr12:107707418
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1078-1508A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707418 | ||||||
chr12:107707794
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1078-1132C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707794 | ||||||
chr12:107707828
|
C | G | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1078-1098C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707828 | ||||||
chr12:107707861
|
G | C | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1078-1065G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707861 | ||||||
chr12:107707883
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1078-1043G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107707883 | ||||||
chr12:107708088
|
A | G | 1 | a0007c0010t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1078-838A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708088 | ||||||
chr12:107708089
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0236 | 2 | HG00408.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1078-837T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708089 | ||||||
chr12:107708127
|
C | T | 1 | a0001c0003t0001g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1078-799C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708127 | ||||||
chr12:107708145
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1078-781T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708145 | ||||||
chr12:107708256
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1078-670C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708256 | ||||||
chr12:107708523
|
T | C | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1078-403T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708523 | ||||||
chr12:107708525
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1078-401G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708525 | ||||||
chr12:107708538
|
G | A | 1 | a0001c0003t0001g0132 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1078-388G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708538 | ||||||
chr12:107708585
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1078-341T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708585 | ||||||
chr12:107708635
|
C | T | 1 | a0002c0002t0002g0175 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1078-291C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708635 | ||||||
chr12:107708776
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1078-150C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708776 | ||||||
chr12:107708777
|
G | A | 2 | a0004c0006t0002g0238a0004c0006t0002g0239 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1078-149G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 11/14 | chr12 | 107708777 | ||||||
chr12:107709510
|
C | CT | 35 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0001g0121others(32): Show | 46 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1290+295dupT | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 107709510 | |||||
chr12:107709527
|
T | A | 1 | a0001c0001t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1290+295T>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709527 | ||||||
chr12:107709527
|
TA | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(57): Show | 85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1290+299delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 107709527 | |||||
chr12:107709528
|
A | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(86): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1290+296A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709528 | ||||||
chr12:107709535
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1290+303T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709535 | ||||||
chr12:107709577
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(58): Show | 87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1290+345C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709577 | ||||||
chr12:107709655
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0225 | 2 | HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1290+423T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709655 | ||||||
chr12:107709806
|
T | C | 1 | a0001c0001t0005g0016 | 3 | HG02622.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1290+574T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709806 | ||||||
chr12:107709813
|
GA | G | 4 | a0001c0001t0004g0084a0001c0005t0004g0017a0001c0005t0004g0044others(1): Show | 5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290+586delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 107709813 | |||||
chr12:107709879
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1291-526C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709879 | ||||||
chr12:107709908
|
T | G | 3 | a0004c0006t0002g0238a0004c0006t0002g0239a0007c0010t0002g0043 | 3 | HG02896.hp1 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1291-497T>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107709908 | ||||||
chr12:107710045
|
A | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1291-360A>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710045 | ||||||
chr12:107710060
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1291-345A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710060 | ||||||
chr12:107710143
|
C | T | 1 | a0001c0001t0012g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-262C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710143 | ||||||
chr12:107710153
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(35): Show | 64 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1291-252T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710153 | ||||||
chr12:107710206
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1291-199C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710206 | ||||||
chr12:107710286
|
A | C | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291-119A>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 13/14 | chr12 | 107710286 | ||||||
chr12:107710540
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0228 | 6 | HG00099.hp2 HG00733.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396+30C>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710540 | ||||||
chr12:107710552
|
T | TA | 16 | a0001c0001t0002g0062a0001c0001t0002g0067a0001c0001t0002g0088others(13): Show | 17 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1396+63dupA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 107710552 | |||||
chr12:107710552
|
T | TAAA | 33 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0025others(30): Show | 57 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1396+61_1396+63dup others(3): Show |
PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 107710552 | |||||
chr12:107710552
|
TA | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(59): Show | 88 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1396+63delA | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr12 | 107710552 | |||||
chr12:107710630
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 63 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1396+120C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710630 | ||||||
chr12:107710640
|
A | G | 1 | a0001c0001t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1396+130A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710640 | ||||||
chr12:107710651
|
T | C | 2 | a0002c0002t0002g0172a0002c0002t0002g0183 | 2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1396+141T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710651 | ||||||
chr12:107710757
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1396+247T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710757 | ||||||
chr12:107710992
|
T | C | 4 | a0001c0003t0001g0137a0001c0003t0001g0138a0001c0003t0001g0140others(1): Show | 4 | HG01243.hp2 HG02486.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396+482T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107710992 | ||||||
chr12:107711200
|
G | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(57): Show | 86 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1396+690G>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711200 | ||||||
chr12:107711358
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(90): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1397-753G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711358 | ||||||
chr12:107711396
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1397-715G>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711396 | ||||||
chr12:107711456
|
C | T | 17 | a0001c0003t0001g0030a0001c0003t0001g0128a0001c0003t0001g0129others(14): Show | 18 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1397-655C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711456 | ||||||
chr12:107711528
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1397-583G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711528 | ||||||
chr12:107711538
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0005g0016 | 4 | HG02083.hp2 HG02622.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397-573C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711538 | ||||||
chr12:107711566
|
C | T | 32 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0036others(29): Show | 41 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1397-545C>T | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711566 | ||||||
chr12:107711609
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(58): Show | 87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1397-502A>G | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711609 | ||||||
chr12:107711747
|
T | C | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1397-364T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711747 | ||||||
chr12:107711778
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1397-333G>A | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107711778 | ||||||
chr12:107712057
|
T | C | 4 | a0001c0001t0004g0084a0001c0005t0004g0017a0001c0005t0004g0044others(1): Show | 5 | HG02647.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1397-54T>C | PWP1 | ENSG00000136045.12 | transcript | ENST00000412830.8 | protein_coding | 14/14 | chr12 | 107712057 |