geneid | 64761 |
---|---|
ensemblid | ENSG00000059378.13 |
hgncid | 21919 |
symbol | PARP12 |
name | poly(ADP-ribose) polymerase family member 12 |
refseq_nuc | NM_022750.4 |
refseq_prot | NP_073587.1 |
ensembl_nuc | ENST00000263549.8 |
ensembl_prot | ENSP00000263549.3 |
mane_status | MANE Select |
chr | chr7 |
start | 140023749 |
end | 140062951 |
strand | - |
ver | v1.2 |
region | chr7:140023749-140062951 |
region5000 | chr7:140018749-140067951 |
regionname0 | PARP12_chr7_140023749_140062951 |
regionname5000 | PARP12_chr7_140018749_140067951 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 701 | 312 | 63 | 62 | 137 | 12 | 36 | 103 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002 | 0/0 | 701 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0003 | 0/0 | 701 | 19 | 5 | 5 | 0 | 1 | 8 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0004 | 0/0 | 701 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0005 | 0/0 | 701 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0006 | 0/0 | 701 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0007 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0008 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0009 | 0/0 | 701 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0010 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2106 | 144 | 15 | 28 | 62 | 9 | 29 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0002 | 0/0 | 2106 | 127 | 29 | 24 | 67 | 3 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0003 | 0/0 | 2106 | 22 | 19 | 2 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0004 | 0/0 | 2106 | 19 | 5 | 5 | 0 | 1 | 8 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0005 | 0/0 | 2106 | 12 | 11 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0006 | 0/0 | 2106 | 8 | 0 | 0 | 8 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0007 | 0/0 | 2106 | 7 | 7 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0008 | 0/1 | 2106 | 5 | 0 | 3 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0009 | 0/0 | 2106 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0010 | 0/0 | 2106 | 3 | 1 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0011 | 0/0 | 2106 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0012 | 0/0 | 2106 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0013 | 0/0 | 2106 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0014 | 0/0 | 2106 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0015 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0016 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0017 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
c0018 | 0/0 | 2106 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 916 | 143 | 33 | 28 | 75 | 3 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0002 | 1/1 | 916 | 142 | 14 | 29 | 60 | 7 | 30 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0003 | 0/0 | 916 | 46 | 29 | 7 | 0 | 1 | 9 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0004 | 0/0 | 916 | 14 | 13 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0005 | 0/0 | 916 | 6 | 0 | 4 | 0 | 1 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0006 | 0/0 | 900 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0007 | 0/0 | 899 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0008 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0009 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0010 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0011 | 0/0 | 916 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0012 | 0/0 | 916 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
t0013 | 0/0 | 916 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0003 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0020 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2106 | 144 | 15 | 28 | 62 | 9 | 29 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0002 | 0/0 | 2106 | 127 | 29 | 24 | 67 | 3 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0003 | 0/0 | 2106 | 22 | 19 | 2 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0006 | 0/0 | 2106 | 8 | 0 | 0 | 8 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0008 | 0/1 | 2106 | 5 | 0 | 3 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0009 | 0/0 | 2106 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0013 | 0/0 | 2106 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0014 | 0/0 | 2106 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0005 | 0/0 | 2106 | 12 | 11 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0007 | 0/0 | 2106 | 7 | 7 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0003c0004 | 0/0 | 2106 | 19 | 5 | 5 | 0 | 1 | 8 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0004c0010 | 0/0 | 2106 | 3 | 1 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0005c0011 | 0/0 | 2106 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0006c0018 | 0/0 | 2106 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0007c0016 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0008c0015 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0009c0012 | 0/0 | 2106 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0010c0017 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 3021 | 131 | 13 | 24 | 59 | 6 | 28 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0001t0003 | 0/0 | 3021 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0001t0005 | 0/0 | 3021 | 6 | 0 | 4 | 0 | 1 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0001t0006 | 0/0 | 3005 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0001t0007 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0001t0010 | 0/0 | 2994 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0001t0011 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0002t0001 | 0/0 | 3021 | 126 | 29 | 23 | 67 | 3 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0002t0012 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0003t0001 | 0/0 | 3021 | 4 | 4 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0003t0003 | 0/0 | 3021 | 17 | 14 | 2 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0003t0008 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0006t0001 | 0/0 | 3021 | 8 | 0 | 0 | 8 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0008t0002 | 0/1 | 3021 | 5 | 0 | 3 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0009t0001 | 0/0 | 3021 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0013t0002 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0001c0014t0001 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0005t0003 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0005t0004 | 0/0 | 3021 | 11 | 10 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0007t0003 | 0/0 | 3021 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0007t0004 | 0/0 | 3021 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0002c0007t0013 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0003c0004t0003 | 0/0 | 3021 | 19 | 5 | 5 | 0 | 1 | 8 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0004c0010t0002 | 0/0 | 3021 | 3 | 1 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0005c0011t0003 | 0/0 | 3021 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0006c0018t0002 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0007c0016t0003 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0008c0015t0009 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0009c0012t0002 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
a0010c0017t0003 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | copy fasta | chr7 | 140018749 | 140067951 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0196 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0006g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0001t0011g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0002t0012g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0003t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0006t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0008t0002g0020 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0008t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0008t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0008t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0009t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0009t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0009t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0009t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0013t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0001c0014t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0005t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0002c0007t0013g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0003c0004t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0004c0010t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0004c0010t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0004c0010t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0005c0011t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0005c0011t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0006c0018t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0007c0016t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0008c0015t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0009c0012t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
a0010c0017t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0235 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00140 | hp2 | a0004 | c0010 | t0002 | g0174 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | FIN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00639 | hp2 | a0003 | c0004 | t0003 | g0070 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00735 | hp2 | a0003 | c0004 | t0003 | g0066 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00738 | hp2 | a0003 | c0004 | t0003 | g0016 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01069 | hp1 | a0003 | c0004 | t0003 | g0018 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01070 | hp1 | a0006 | c0018 | t0002 | g0277 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01071 | hp2 | a0003 | c0004 | t0003 | g0018 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01074 | hp1 | a0004 | c0010 | t0002 | g0124 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01106 | hp1 | a0001 | c0009 | t0001 | g0267 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01109 | hp1 | a0001 | c0014 | t0001 | g0248 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0026 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01192 | hp2 | a0001 | c0008 | t0002 | g0049 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01243 | hp2 | a0001 | c0008 | t0002 | g0112 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0173 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01261 | hp2 | a0002 | c0005 | t0004 | g0286 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01358 | hp1 | a0001 | c0008 | t0002 | g0082 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0170 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01433 | hp1 | a0001 | c0009 | t0001 | g0273 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01433 | hp2 | a0001 | c0009 | t0001 | g0264 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01496 | hp1 | a0001 | c0009 | t0001 | g0271 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0172 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0171 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0043 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0130 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0043 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01884 | hp1 | a0001 | c0003 | t0003 | g0193 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01952 | hp1 | a0001 | c0003 | t0003 | g0029 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02055 | hp1 | a0004 | c0010 | t0002 | g0061 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02055 | hp2 | a0005 | c0011 | t0003 | g0188 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02080 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02083 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02129 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02145 | hp2 | a0002 | c0005 | t0004 | g0282 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02257 | hp2 | a0001 | c0003 | t0003 | g0029 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02258 | hp1 | a0001 | c0003 | t0003 | g0136 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0259 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02523 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02615 | hp1 | a0003 | c0004 | t0003 | g0017 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02615 | hp2 | a0002 | c0007 | t0003 | g0181 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02622 | hp2 | a0001 | c0003 | t0003 | g0195 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0138 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02698 | hp1 | a0003 | c0004 | t0003 | g0071 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02717 | hp1 | a0001 | c0003 | t0003 | g0137 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02738 | hp2 | a0003 | c0004 | t0003 | g0068 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02809 | hp1 | a0002 | c0005 | t0004 | g0279 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02809 | hp2 | a0002 | c0007 | t0003 | g0187 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02818 | hp1 | a0003 | c0004 | t0003 | g0017 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02818 | hp2 | a0001 | c0003 | t0003 | g0073 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02886 | hp2 | a0002 | c0005 | t0004 | g0284 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02896 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02897 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02965 | hp1 | a0003 | c0004 | t0003 | g0065 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02965 | hp2 | a0002 | c0005 | t0004 | g0278 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02970 | hp1 | a0002 | c0005 | t0004 | g0285 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02976 | hp1 | a0002 | c0005 | t0003 | g0160 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02976 | hp2 | a0007 | c0016 | t0003 | g0164 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03041 | hp2 | a0002 | c0005 | t0004 | g0044 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03098 | hp2 | a0010 | c0017 | t0003 | g0276 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03130 | hp1 | a0002 | c0007 | t0004 | g0290 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0194 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03139 | hp2 | a0002 | c0005 | t0004 | g0283 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03209 | hp1 | a0002 | c0007 | t0004 | g0289 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03225 | hp1 | a0001 | c0003 | t0008 | g0140 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0159 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03486 | hp1 | a0002 | c0005 | t0004 | g0281 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03490 | hp1 | a0001 | c0008 | t0002 | g0020 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03516 | hp1 | a0002 | c0007 | t0004 | g0287 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0074 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03654 | hp2 | a0001 | c0013 | t0002 | g0051 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0168 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03688 | hp1 | a0003 | c0004 | t0003 | g0069 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03710 | hp2 | a0001 | c0003 | t0003 | g0026 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03927 | hp2 | a0003 | c0004 | t0003 | g0067 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04115 | hp1 | a0003 | c0004 | t0003 | g0019 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04184 | hp1 | a0003 | c0004 | t0003 | g0072 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04199 | hp2 | a0003 | c0004 | t0003 | g0135 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04204 | hp2 | a0003 | c0004 | t0003 | g0019 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18522 | hp1 | a0003 | c0004 | t0003 | g0063 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18522 | hp2 | a0002 | c0005 | t0004 | g0044 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | CHB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18906 | hp1 | a0001 | c0003 | t0003 | g0144 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18906 | hp2 | a0002 | c0005 | t0004 | g0280 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18952 | hp1 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18961 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18969 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19001 | hp2 | a0001 | c0001 | t0010 | g0099 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19006 | hp2 | a0001 | c0006 | t0001 | g0226 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19043 | hp1 | a0002 | c0007 | t0003 | g0180 | AFR | LWK | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | LWK | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19062 | hp2 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19080 | hp2 | a0001 | c0001 | t0011 | g0161 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19085 | hp2 | a0009 | c0012 | t0002 | g0078 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA19240 | hp2 | a0003 | c0004 | t0003 | g0064 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | ASW | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20129 | hp2 | a0005 | c0011 | t0003 | g0191 | AFR | ASW | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20805 | hp1 | a0003 | c0004 | t0003 | g0016 | EUR | TSI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | TSI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | GIH | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | GIH | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01123 | hp1 | a0001 | c0002 | t0012 | g0252 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02486 | hp1 | a0002 | c0007 | t0013 | g0288 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02486 | hp2 | a0008 | c0015 | t0009 | g0192 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG02559 | hp2 | a0001 | c0003 | t0003 | g0139 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20300 | hp1 | a0001 | c0003 | t0003 | g0183 | AFR | USA | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | USA | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
homoSapiens_chm13v2 | hp1 | a0001 | c0008 | t0002 | g0020 | REF | REF | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0196 | REF | REF | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:140024807
|
G | A | 1 | a0005 | 2 | HG02055.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1859C>T | p.Ala620Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 1963/3021 | 1859/2106 | 620/701 | chr7 | 140024807 | ||
chr7:140034269
|
C | T | 1 | a0003 | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
missense_variant | MODERATE | c.1387G>A | p.Val463Met | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/12 | 1491/3021 | 1387/2106 | 463/701 | chr7 | 140034269 | ||
chr7:140046993
|
C | T | 4 | a0002a0005a0007others(1): Show | 23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
missense_variant | MODERATE | c.877G>A | p.Val293Ile | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/12 | 981/3021 | 877/2106 | 293/701 | chr7 | 140046993 | ||
chr7:140056988
|
A | C | 1 | a0009 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.628T>G | p.Leu210Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/12 | 732/3021 | 628/2106 | 210/701 | chr7 | 140056988 | ||
chr7:140057912
|
C | A | 1 | a0004 | 3 | HG00140.hp2 HG01074.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.449G>T | p.Trp150Leu | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/12 | 553/3021 | 449/2106 | 150/701 | chr7 | 140057912 | ||
chr7:140057951
|
T | C | 1 | a0008 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.410A>G | p.Tyr137Cys | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/12 | 514/3021 | 410/2106 | 137/701 | chr7 | 140057951 | ||
chr7:140058002
|
G | A | 1 | a0007 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.359C>T | p.Thr120Ile | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/12 | 463/3021 | 359/2106 | 120/701 | chr7 | 140058002 | ||
chr7:140062642
|
G | A | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.206C>T | p.Ala69Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 310/3021 | 206/2106 | 69/701 | chr7 | 140062642 | ||
chr7:140062778
|
G | C | 1 | a0006 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.70C>G | p.Pro24Ala | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 174/3021 | 70/2106 | 24/701 | chr7 | 140062778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:140024710
|
C | T | 1 | a0001c0014 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1956G>A | p.Val652Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2060/3021 | 1956/2106 | 652/701 | chr7 | 140024710 | ||
chr7:140024755
|
C | G | 4 | a0002c0005a0005c0011a0007c0016others(1): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.1911G>C | p.Pro637Pro | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2015/3021 | 1911/2106 | 637/701 | chr7 | 140024755 | ||
chr7:140024755
|
C | T | 6 | a0001c0002a0001c0003a0001c0009others(3): Show | 162 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(159): Show |
synonymous_variant | LOW | c.1911G>A | p.Pro637Pro | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2015/3021 | 1911/2106 | 637/701 | chr7 | 140024755 | ||
chr7:140026321
|
G | A | 2 | a0001c0008a0001c0009 | 9 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(6): Show |
synonymous_variant | LOW | c.1656C>T | p.Asn552Asn | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/12 | 1760/3021 | 1656/2106 | 552/701 | chr7 | 140026321 | ||
chr7:140027335
|
G | A | 4 | a0001c0002a0001c0006a0001c0009others(1): Show | 140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
synonymous_variant | LOW | c.1569C>T | p.Phe523Phe | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/12 | 1673/3021 | 1569/2106 | 523/701 | chr7 | 140027335 | ||
chr7:140037851
|
C | G | 1 | a0001c0013 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1188G>C | p.Thr396Thr | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/12 | 1292/3021 | 1188/2106 | 396/701 | chr7 | 140037851 | ||
chr7:140041773
|
G | A | 1 | a0007c0016 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1053C>T | p.Tyr351Tyr | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/12 | 1157/3021 | 1053/2106 | 351/701 | chr7 | 140041773 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:140023775
|
TACTCTTT others(20): Show |
T | 1 | a0001c0001t0010 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*758_*784delCTTGTG others(21): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 758 | chr7 | 140023775 | |||||
chr7:140023796
|
G | A | 2 | a0001c0001t0005a0001c0001t0006 | 8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 764 | chr7 | 140023796 | |||||
chr7:140023874
|
C | T | 1 | a0008c0015t0009 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 686 | chr7 | 140023874 | |||||
chr7:140023942
|
C | T | 2 | a0001c0001t0005a0001c0001t0006 | 8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*618G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 618 | chr7 | 140023942 | |||||
chr7:140024020
|
T | C | 1 | a0001c0002t0012 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 540 | chr7 | 140024020 | |||||
chr7:140024177
|
A | G | 1 | a0001c0003t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 383 | chr7 | 140024177 | |||||
chr7:140024270
|
T | C | 1 | a0001c0001t0011 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*290A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 290 | chr7 | 140024270 | |||||
chr7:140024362
|
C | T | 1 | a0002c0007t0013 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 198 | chr7 | 140024362 | |||||
chr7:140024369
|
A | G | 21 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(18): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 191 | chr7 | 140024369 | |||||
chr7:140024472
|
TAAAAGTT others(10): Show |
T | 1 | a0001c0001t0007 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71_*87delTTTAAACA others(9): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 71 | chr7 | 140024472 | |||||
chr7:140024558
|
G | A | 6 | a0001c0002t0001a0001c0002t0012a0001c0003t0001others(3): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2 | chr7 | 140024558 | |||||
chr7:140062885
|
CGACGCGG others(9): Show |
C | 1 | a0001c0001t0006 | 2 | HG01515.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-54_-39delCGCCGCCG others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 39 | chr7 | 140062885 | |||||
chr7:140062915
|
G | C | 3 | a0002c0005t0004a0002c0007t0004a0002c0007t0013 | 15 | HG01261.hp2 HG02145.hp2 HG02486.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-68C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 68 | chr7 | 140062915 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:140024942
|
G | C | 17 | a0001c0002t0001g0007a0001c0002t0001g0038a0001c0002t0001g0167others(14): Show | 21 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1781-57C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140024942 | ||||||
chr7:140025017
|
C | T | 1 | a0001c0002t0001g0223 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1781-132G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025017 | ||||||
chr7:140025358
|
C | T | 12 | a0001c0003t0003g0026a0001c0003t0003g0030a0001c0003t0003g0073others(9): Show | 14 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1781-473G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025358 | ||||||
chr7:140025400
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1781-515T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025400 | ||||||
chr7:140025468
|
T | C | 1 | a0002c0005t0004g0044 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1781-583A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025468 | ||||||
chr7:140025508
|
A | G | 11 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(8): Show | 12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1781-623T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025508 | ||||||
chr7:140025780
|
A | C | 1 | a0001c0002t0001g0011 | 3 | NA18968.hp2 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1780+417T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025780 | ||||||
chr7:140025894
|
G | A | 11 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(8): Show | 12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1780+303C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025894 | ||||||
chr7:140026143
|
T | C | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1780+54A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140026143 | ||||||
chr7:140026407
|
G | A | 120 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(117): Show | 154 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1629-59C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026407 | ||||||
chr7:140026420
|
A | C | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-72T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026420 | ||||||
chr7:140026421
|
C | A | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-73G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026421 | ||||||
chr7:140026499
|
A | AG | 289 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(286): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1629-152dupC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026499 | ||||||
chr7:140026579
|
C | A | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1629-231G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026579 | ||||||
chr7:140026601
|
A | C | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-253T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026601 | ||||||
chr7:140026605
|
G | C | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-257C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026605 | ||||||
chr7:140026654
|
A | C | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-306T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026654 | ||||||
chr7:140026667
|
A | G | 170 | a0001c0001t0003g0134a0001c0001t0003g0185a0001c0001t0005g0168others(167): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.1629-319T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026667 | ||||||
chr7:140026681
|
T | G | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-333A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026681 | ||||||
chr7:140026935
|
C | A | 1 | a0001c0001t0002g0115 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1628+341G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026935 | ||||||
chr7:140026973
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0111 | 3 | HG00099.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1628+303A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026973 | ||||||
chr7:140027120
|
G | C | 2 | a0001c0002t0001g0249a0001c0002t0001g0254 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1628+156C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027120 | ||||||
chr7:140027140
|
C | A | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1628+136G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027140 | ||||||
chr7:140027155
|
C | T | 1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1628+121G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027155 | ||||||
chr7:140027243
|
T | C | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1628+33A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027243 | ||||||
chr7:140027247
|
C | G | 1 | a0001c0002t0001g0011 | 3 | NA18968.hp2 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1628+29G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027247 | ||||||
chr7:140027471
|
C | T | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1498-65G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027471 | ||||||
chr7:140027528
|
C | A | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1498-122G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027528 | ||||||
chr7:140027543
|
T | C | 7 | a0002c0007t0003g0180a0002c0007t0003g0181a0002c0007t0003g0187others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-137A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027543 | ||||||
chr7:140027567
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0126 | 2 | NA18955.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1498-161C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027567 | ||||||
chr7:140027584
|
A | T | 1 | a0001c0001t0010g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1498-178T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027584 | ||||||
chr7:140027585
|
T | C | 2 | a0001c0001t0002g0244a0001c0002t0012g0252 | 2 | HG01123.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1498-179A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027585 | ||||||
chr7:140027703
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0002g0094 | 3 | HG03491.hp2 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1498-297G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027703 | ||||||
chr7:140027721
|
T | A | 1 | a0001c0002t0001g0207 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1498-315A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027721 | ||||||
chr7:140027870
|
T | C | 154 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(151): Show | 195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1498-464A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027870 | ||||||
chr7:140027880
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1498-474T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027880 | ||||||
chr7:140027981
|
T | C | 2 | a0001c0001t0005g0169a0001c0001t0005g0171 | 2 | HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1498-575A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027981 | ||||||
chr7:140028246
|
T | C | 134 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0244others(131): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1497+367A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028246 | ||||||
chr7:140028290
|
C | T | 3 | a0003c0004t0003g0017a0003c0004t0003g0065a0003c0004t0003g0066 | 4 | HG00735.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+323G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028290 | ||||||
chr7:140028518
|
G | A | 1 | a0001c0003t0003g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1497+95C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028518 | ||||||
chr7:140028600
|
A | G | 3 | a0001c0002t0001g0218a0001c0002t0001g0219a0001c0002t0001g0224 | 3 | HG00423.hp2 HG02074.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1497+13T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028600 | ||||||
chr7:140028752
|
G | C | 2 | a0001c0001t0002g0244a0001c0002t0012g0252 | 2 | HG01123.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1422-64C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140028752 | ||||||
chr7:140028784
|
A | C | 125 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(122): Show | 164 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1422-96T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140028784 | ||||||
chr7:140028916
|
C | T | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422-228G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140028916 | ||||||
chr7:140029340
|
T | C | 1 | a0003c0004t0003g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1422-652A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029340 | ||||||
chr7:140029414
|
C | G | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1422-726G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029414 | ||||||
chr7:140029527
|
A | G | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422-839T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029527 | ||||||
chr7:140029631
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1422-943G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029631 | ||||||
chr7:140029762
|
A | G | 12 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(9): Show | 13 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1422-1074T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029762 | ||||||
chr7:140029773
|
G | A | 8 | a0001c0001t0005g0168a0002c0007t0003g0180a0002c0007t0003g0181others(5): Show | 8 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422-1085C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029773 | ||||||
chr7:140030026
|
G | C | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422-1338C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030026 | ||||||
chr7:140030230
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1422-1542T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030230 | ||||||
chr7:140030451
|
A | T | 1 | a0001c0002t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1422-1763T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030451 | ||||||
chr7:140030467
|
G | A | 1 | a0005c0011t0003g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1422-1779C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030467 | ||||||
chr7:140030471
|
G | A | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1422-1783C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030471 | ||||||
chr7:140030522
|
C | T | 1 | a0001c0002t0001g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1422-1834G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030522 | ||||||
chr7:140030548
|
A | C | 5 | a0001c0001t0002g0093a0001c0001t0002g0104a0001c0001t0002g0128others(2): Show | 5 | NA18941.hp1 NA18943.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1422-1860T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030548 | ||||||
chr7:140030605
|
A | ACATACAT others(5): Show |
15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1422-1929_1422-191 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030605 | ||||||
chr7:140030605
|
ACATACAT others(5): Show |
A | 1 | a0001c0001t0002g0149 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1422-1929_1422-191 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030605 | ||||||
chr7:140030700
|
C | G | 139 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(136): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1422-2012G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030700 | ||||||
chr7:140030702
|
T | C | 3 | a0001c0002t0001g0033a0001c0002t0001g0202a0001c0002t0001g0211 | 4 | HG01993.hp1 HG02148.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422-2014A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030702 | ||||||
chr7:140030773
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1422-2085T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030773 | ||||||
chr7:140030827
|
G | C | 1 | a0001c0002t0001g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1422-2139C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030827 | ||||||
chr7:140030970
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1422-2282A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030970 | ||||||
chr7:140031487
|
T | C | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1421+2748A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031487 | ||||||
chr7:140031730
|
A | C | 2 | a0001c0002t0001g0218a0001c0002t0001g0224 | 2 | HG00423.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1421+2505T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031730 | ||||||
chr7:140031838
|
G | C | 1 | a0001c0001t0002g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1421+2397C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031838 | ||||||
chr7:140031909
|
G | A | 196 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0057others(193): Show | 250 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1421+2326C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031909 | ||||||
chr7:140032105
|
C | G | 1 | a0002c0005t0004g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1421+2130G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032105 | ||||||
chr7:140032153
|
G | C | 2 | a0001c0001t0002g0095a0001c0001t0002g0106 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1421+2082C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032153 | ||||||
chr7:140032160
|
C | A | 1 | a0001c0001t0002g0129 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1421+2075G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032160 | ||||||
chr7:140032277
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0185 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+1958T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032277 | ||||||
chr7:140032335
|
T | C | 1 | a0001c0003t0003g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1421+1900A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032335 | ||||||
chr7:140032349
|
TA | T | 9 | a0001c0002t0001g0204a0001c0002t0001g0208a0002c0007t0003g0180others(6): Show | 9 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1421+1885delT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032349 | ||||||
chr7:140032430
|
G | C | 1 | a0001c0001t0002g0080 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1421+1805C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032430 | ||||||
chr7:140032467
|
G | A | 1 | a0001c0002t0001g0201 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1421+1768C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032467 | ||||||
chr7:140032702
|
A | G | 5 | a0001c0001t0002g0076a0001c0001t0002g0083a0001c0001t0002g0100others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421+1533T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032702 | ||||||
chr7:140033030
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1421+1205G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033030 | ||||||
chr7:140033098
|
G | A | 1 | a0001c0002t0001g0265 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1421+1137C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033098 | ||||||
chr7:140033182
|
T | G | 1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1421+1053A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033182 | ||||||
chr7:140033371
|
C | G | 1 | a0001c0001t0002g0233 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1421+864G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033371 | ||||||
chr7:140033454
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0185 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+781T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033454 | ||||||
chr7:140033612
|
A | G | 3 | a0001c0003t0003g0193a0001c0003t0003g0194a0001c0003t0003g0195 | 3 | HG01884.hp1 HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1421+623T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033612 | ||||||
chr7:140033654
|
C | T | 16 | a0001c0001t0002g0001a0001c0001t0002g0077a0001c0001t0002g0145others(13): Show | 22 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1421+581G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033654 | ||||||
chr7:140033782
|
G | A | 4 | a0001c0003t0003g0030a0001c0003t0003g0193a0001c0003t0003g0194others(1): Show | 5 | HG01884.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421+453C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033782 | ||||||
chr7:140034509
|
T | C | 11 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(8): Show | 12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1325-178A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034509 | ||||||
chr7:140034573
|
C | T | 168 | a0001c0001t0002g0244a0001c0001t0003g0134a0001c0001t0003g0185others(165): Show | 212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1325-242G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034573 | ||||||
chr7:140034633
|
A | AT | 5 | a0001c0002t0001g0041a0001c0002t0001g0236a0001c0002t0001g0250others(2): Show | 7 | HG01952.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-303dupA | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034633 | ||||||
chr7:140034768
|
C | A | 7 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(4): Show | 8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1325-437G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034768 | ||||||
chr7:140034897
|
C | A | 154 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(151): Show | 195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1325-566G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034897 | ||||||
chr7:140035226
|
A | G | 1 | a0001c0002t0001g0210 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1325-895T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035226 | ||||||
chr7:140035276
|
T | C | 13 | a0001c0003t0003g0026a0001c0003t0003g0030a0001c0003t0003g0073others(10): Show | 15 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1325-945A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035276 | ||||||
chr7:140035331
|
G | C | 1 | a0001c0002t0001g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1325-1000C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035331 | ||||||
chr7:140035334
|
G | A | 1 | a0001c0001t0002g0151 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1325-1003C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035334 | ||||||
chr7:140035483
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1325-1152T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035483 | ||||||
chr7:140035793
|
A | G | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1325-1462T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035793 | ||||||
chr7:140035806
|
T | C | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1325-1475A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035806 | ||||||
chr7:140035837
|
A | G | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1325-1506T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035837 | ||||||
chr7:140035842
|
G | GGAGGAAG others(17): Show |
2 | a0001c0001t0003g0134a0001c0001t0003g0185 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1325-1535_1325-151 others(28): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035842 | ||||||
chr7:140035884
|
A | G | 168 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(165): Show | 213 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1325-1553T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035884 | ||||||
chr7:140035886
|
A | G | 168 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(165): Show | 213 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1325-1555T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035886 | ||||||
chr7:140035890
|
AGAGGAGG others(32): Show |
A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1598_1325-156 others(43): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035890 | ||||||
chr7:140035896
|
G | A | 167 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(164): Show | 212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1325-1565C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035896 | ||||||
chr7:140035902
|
C | A | 1 | a0003c0004t0003g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1325-1571G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035902 | ||||||
chr7:140035902
|
C | G | 167 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(164): Show | 212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1325-1571G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035902 | ||||||
chr7:140035908
|
G | A | 153 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(150): Show | 194 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1325-1577C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035908 | ||||||
chr7:140035910
|
A | G | 14 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(11): Show | 18 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1325-1579T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035910 | ||||||
chr7:140035912
|
GACA | G | 16 | a0001c0002t0012g0252a0002c0005t0003g0160a0002c0005t0004g0044others(13): Show | 17 | HG01123.hp1 HG01261.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1325-1584_1325-158 others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035912 | ||||||
chr7:140035914
|
C | A | 151 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(148): Show | 195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1325-1583G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035914 | ||||||
chr7:140035915
|
A | G | 151 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(148): Show | 195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1325-1584T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035915 | ||||||
chr7:140035917
|
G | A | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1325-1586C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035917 | ||||||
chr7:140035923
|
G | A | 1 | a0001c0002t0012g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1592C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035923 | ||||||
chr7:140035926
|
C | G | 16 | a0001c0002t0012g0252a0002c0005t0003g0160a0002c0005t0004g0044others(13): Show | 17 | HG01123.hp1 HG01261.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1325-1595G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035926 | ||||||
chr7:140035926
|
CAAG | C | 128 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(125): Show | 166 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1325-1598_1325-159 others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035926 | ||||||
chr7:140035926
|
CAAGGAG | C | 5 | a0001c0002t0001g0212a0001c0002t0001g0243a0001c0002t0001g0275others(2): Show | 6 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1601_1325-159 others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035926 | ||||||
chr7:140035927
|
A | G | 5 | a0001c0002t0012g0252a0001c0003t0003g0030a0001c0003t0003g0193others(2): Show | 6 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1596T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035927 | ||||||
chr7:140035927
|
AAGG | A | 6 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0121others(3): Show | 6 | HG00438.hp1 HG00735.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325-1599_1325-159 others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035927 | ||||||
chr7:140035927
|
AAGGAGGA others(8): Show |
A | 1 | a0003c0004t0003g0017 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1325-1611_1325-159 others(19): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035927 | ||||||
chr7:140035929
|
G | A | 1 | a0001c0002t0012g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1598C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035929 | ||||||
chr7:140035929
|
G | C | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1325-1598C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035929 | ||||||
chr7:140035935
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1604C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035935 | ||||||
chr7:140035935
|
G | GGAGGAGG others(11): Show |
1 | a0001c0001t0002g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1325-1622_1325-160 others(22): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035935 | ||||||
chr7:140035938
|
G | C | 17 | a0001c0003t0003g0030a0001c0003t0003g0193a0001c0003t0003g0194others(14): Show | 21 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1325-1607C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035938 | ||||||
chr7:140035939
|
G | A | 17 | a0001c0003t0003g0030a0001c0003t0003g0193a0001c0003t0003g0194others(14): Show | 21 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1325-1608C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035939 | ||||||
chr7:140035941
|
G | C | 144 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(141): Show | 183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1325-1610C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035941 | ||||||
chr7:140035942
|
G | A | 38 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(35): Show | 41 | HG01123.hp2 HG01175.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.1325-1611C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035942 | ||||||
chr7:140035944
|
G | C | 5 | a0001c0002t0001g0212a0001c0002t0001g0243a0001c0002t0001g0275others(2): Show | 6 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1613C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035944 | ||||||
chr7:140035944
|
GGAGGAGG others(2): Show |
G | 8 | a0003c0004t0003g0016a0003c0004t0003g0065a0003c0004t0003g0067others(5): Show | 9 | HG00639.hp2 HG00738.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-1622_1325-161 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035944 | ||||||
chr7:140035945
|
G | A | 5 | a0001c0002t0001g0212a0001c0002t0001g0243a0001c0002t0001g0275others(2): Show | 6 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1614C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035945 | ||||||
chr7:140035947
|
GGAGGAC | G | 3 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0135 | 5 | HG01069.hp1 HG01071.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-1622_1325-161 others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035947 | ||||||
chr7:140035949
|
A | G | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1618T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035949 | ||||||
chr7:140035953
|
C | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1622G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035953 | ||||||
chr7:140035953
|
C | G | 10 | a0001c0002t0001g0212a0001c0002t0001g0243a0001c0002t0001g0275others(7): Show | 12 | HG01884.hp1 HG02080.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1325-1622G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035953 | ||||||
chr7:140035954
|
G | A | 137 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(134): Show | 175 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1325-1623C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035954 | ||||||
chr7:140035959
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1628C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035959 | ||||||
chr7:140035962
|
G | C | 1 | a0003c0004t0003g0063 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1325-1631C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035962 | ||||||
chr7:140035965
|
G | C | 6 | a0001c0002t0012g0252a0001c0003t0003g0030a0001c0003t0003g0193others(3): Show | 7 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-1634C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035965 | ||||||
chr7:140035966
|
G | A | 1 | a0001c0002t0012g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1635C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035966 | ||||||
chr7:140035966
|
GAGGACGA others(56): Show |
G | 1 | a0003c0004t0003g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1324+1686_1325-163 others(67): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035966 | ||||||
chr7:140035971
|
C | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1640G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035971 | ||||||
chr7:140035971
|
C | G | 149 | a0001c0001t0002g0244a0001c0001t0005g0168a0001c0001t0005g0169others(146): Show | 190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1325-1640G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035971 | ||||||
chr7:140035971
|
CGAGGAGG others(2): Show |
C | 7 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0046others(4): Show | 9 | NA18962.hp1 NA18975.hp1 NA19003.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-1649_1325-164 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035971 | ||||||
chr7:140035977
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1646C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035977 | ||||||
chr7:140035977
|
G | C | 8 | a0001c0009t0001g0264a0002c0007t0003g0180a0002c0007t0003g0181others(5): Show | 9 | HG01433.hp2 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1325-1646C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035977 | ||||||
chr7:140035980
|
G | C | 127 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(124): Show | 165 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1325-1649C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035980 | ||||||
chr7:140035983
|
G | C | 1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1652C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035983 | ||||||
chr7:140035984
|
GAGGAGGA others(38): Show |
G | 7 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(4): Show | 8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+1686_1325-165 others(49): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035984 | ||||||
chr7:140035986
|
G | C | 4 | a0001c0003t0003g0030a0001c0003t0003g0193a0001c0003t0003g0194others(1): Show | 5 | HG01884.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-1655C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035986 | ||||||
chr7:140035987
|
GAGGAGGA others(8): Show |
G | 2 | a0001c0001t0003g0185a0001c0008t0002g0049 | 2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1325-1671_1325-165 others(19): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035987 | ||||||
chr7:140035987
|
GAGGAGGA others(17): Show |
G | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1325-1680_1325-165 others(28): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035987 | ||||||
chr7:140035987
|
GAGGAGGA others(62): Show |
G | 6 | a0001c0002t0001g0190a0001c0002t0001g0212a0001c0002t0001g0243others(3): Show | 7 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324+1659_1325-165 others(73): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035987 | ||||||
chr7:140035989
|
G | C | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1658C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035989 | ||||||
chr7:140035990
|
GAGGAGGA others(5): Show |
G | 2 | a0004c0010t0002g0061a0004c0010t0002g0174 | 2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1325-1671_1325-166 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | ||||||
chr7:140035990
|
GAGGAGGA others(14): Show |
G | 1 | a0004c0010t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1325-1680_1325-166 others(25): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | ||||||
chr7:140035990
|
GAGGAGGA others(23): Show |
G | 2 | a0002c0007t0003g0180a0002c0007t0003g0181 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1325-1689_1325-166 others(34): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | ||||||
chr7:140035990
|
GAGGAGGA others(32): Show |
G | 1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+1686_1325-166 others(43): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | ||||||
chr7:140035992
|
G | C | 1 | a0001c0002t0012g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1661C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035992 | ||||||
chr7:140035993
|
G | GAGGAGGA others(2): Show |
7 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0083others(4): Show | 7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325-1671_1325-166 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035993
|
GAGGAGGA others(2): Show |
G | 30 | a0001c0001t0002g0005a0001c0001t0002g0015a0001c0001t0002g0023others(27): Show | 39 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1325-1671_1325-166 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035993
|
GAGGAGGA others(11): Show |
G | 2 | a0001c0001t0002g0092a0001c0001t0002g0131 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1325-1680_1325-166 others(22): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035993
|
GAGGAGGA others(20): Show |
G | 1 | a0001c0001t0002g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1325-1689_1325-166 others(31): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035993
|
GAGGAGGA others(38): Show |
G | 13 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(10): Show | 17 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1324+1677_1325-166 others(49): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035993
|
GAGGAGGA others(47): Show |
G | 2 | a0003c0004t0003g0063a0003c0004t0003g0064 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1324+1668_1325-166 others(58): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035993
|
GAGGAGGA others(56): Show |
G | 2 | a0001c0002t0001g0256a0001c0009t0001g0264 | 2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1324+1659_1325-166 others(67): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | ||||||
chr7:140035995
|
G | C | 1 | a0002c0007t0004g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1325-1664C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035995 | ||||||
chr7:140035996
|
GAGGAGAA others(8): Show |
G | 2 | a0002c0007t0004g0287a0002c0007t0004g0289 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1325-1680_1325-166 others(19): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | ||||||
chr7:140035996
|
GAGGAGAA others(26): Show |
G | 8 | a0001c0003t0003g0026a0001c0003t0003g0073a0001c0003t0003g0074others(5): Show | 9 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324+1686_1325-166 others(37): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | ||||||
chr7:140035996
|
GAGGAGAA others(35): Show |
G | 13 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0279others(10): Show | 14 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1324+1677_1325-166 others(46): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | ||||||
chr7:140035996
|
GAGGAGAA others(44): Show |
G | 1 | a0001c0003t0003g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1324+1668_1325-166 others(55): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | ||||||
chr7:140035996
|
GAGGAGAA others(53): Show |
G | 102 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(99): Show | 138 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1324+1659_1325-166 others(64): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | ||||||
chr7:140035999
|
GAGAAGGA others(5): Show |
G | 1 | a0002c0007t0004g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1325-1680_1325-166 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035999 | ||||||
chr7:140035999
|
GAGAAGGA others(32): Show |
G | 1 | a0002c0005t0004g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1324+1677_1325-166 others(43): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035999 | ||||||
chr7:140035999
|
GAGAAGGA others(41): Show |
G | 5 | a0001c0002t0012g0252a0001c0003t0003g0030a0001c0003t0003g0193others(2): Show | 6 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+1668_1325-166 others(52): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035999 | ||||||
chr7:140036001
|
G | C | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1670C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036001 | ||||||
chr7:140036002
|
A | G | 1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1671T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036002 | ||||||
chr7:140036006
|
A | G | 1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1675T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036006 | ||||||
chr7:140036007
|
G | C | 1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1676C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036007 | ||||||
chr7:140036011
|
A | G | 1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1680T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036011 | ||||||
chr7:140036016
|
G | C | 2 | a0002c0007t0004g0287a0002c0007t0004g0289 | 2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1325-1685C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036016 | ||||||
chr7:140036020
|
A | G | 5 | a0002c0007t0004g0287a0002c0007t0004g0289a0002c0007t0004g0290others(2): Show | 5 | HG02486.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-1689T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036020 | ||||||
chr7:140036029
|
A | G | 3 | a0002c0007t0004g0287a0002c0007t0004g0289a0008c0015t0009g0192 | 3 | HG02486.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1324+1686T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036029 | ||||||
chr7:140036031
|
G | C | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1684C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036031 | ||||||
chr7:140036034
|
G | C | 8 | a0001c0003t0003g0026a0001c0003t0003g0073a0001c0003t0003g0074others(5): Show | 9 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324+1681C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036034 | ||||||
chr7:140036038
|
A | G | 10 | a0001c0003t0003g0026a0001c0003t0003g0073a0001c0003t0003g0074others(7): Show | 11 | HG00735.hp2 HG01175.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324+1677T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036038 | ||||||
chr7:140036046
|
G | A | 1 | a0007c0016t0003g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1324+1669C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036046 | ||||||
chr7:140036047
|
A | G | 9 | a0001c0003t0003g0026a0001c0003t0003g0073a0001c0003t0003g0074others(6): Show | 10 | HG01175.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324+1668T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036047 | ||||||
chr7:140036056
|
A | G | 1 | a0001c0002t0012g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1324+1659T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036056 | ||||||
chr7:140036065
|
A | G | 2 | a0001c0002t0001g0255a0001c0002t0001g0259 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1324+1650T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036065 | ||||||
chr7:140036089
|
A | G | 1 | a0005c0011t0003g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1324+1626T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036089 | ||||||
chr7:140036116
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1324+1599G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036116 | ||||||
chr7:140036146
|
G | T | 1 | a0001c0001t0002g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1324+1569C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036146 | ||||||
chr7:140036159
|
C | T | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1556G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036159 | ||||||
chr7:140036166
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1324+1549G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036166 | ||||||
chr7:140036166
|
C | T | 7 | a0001c0003t0003g0026a0001c0003t0003g0073a0001c0003t0003g0074others(4): Show | 8 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+1549G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036166 | ||||||
chr7:140036232
|
A | C | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1324+1483T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036232 | ||||||
chr7:140036275
|
T | A | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1324+1440A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036275 | ||||||
chr7:140036353
|
T | G | 1 | a0001c0001t0002g0090 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1324+1362A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036353 | ||||||
chr7:140036484
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1231C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036484 | ||||||
chr7:140036610
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1324+1105G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036610 | ||||||
chr7:140036634
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1081C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036634 | ||||||
chr7:140036764
|
G | C | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1324+951C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036764 | ||||||
chr7:140036822
|
T | TA | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324+892dupT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036822 | ||||||
chr7:140036822
|
TA | T | 125 | a0001c0001t0002g0105a0001c0001t0002g0244a0001c0002t0001g0004others(122): Show | 164 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1324+892delT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036822 | ||||||
chr7:140036885
|
C | A | 1 | a0001c0002t0001g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1324+830G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036885 | ||||||
chr7:140036997
|
T | C | 6 | a0001c0001t0002g0056a0001c0001t0002g0103a0001c0001t0002g0116others(3): Show | 6 | HG01192.hp1 HG01516.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324+718A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036997 | ||||||
chr7:140037034
|
G | A | 17 | a0001c0002t0001g0007a0001c0002t0001g0038a0001c0002t0001g0167others(14): Show | 21 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1324+681C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037034 | ||||||
chr7:140037051
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1324+664C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037051 | ||||||
chr7:140037255
|
C | T | 2 | a0001c0002t0001g0258a0001c0002t0001g0263 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1324+460G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037255 | ||||||
chr7:140037256
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+459C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037256 | ||||||
chr7:140037424
|
G | A | 2 | a0001c0001t0003g0134a0001c0001t0003g0185 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1324+291C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037424 | ||||||
chr7:140037432
|
C | A | 1 | a0001c0009t0001g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1324+283G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037432 | ||||||
chr7:140037544
|
C | T | 131 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(128): Show | 170 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1324+171G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037544 | ||||||
chr7:140037559
|
A | G | 1 | a0001c0001t0002g0025 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1324+156T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037559 | ||||||
chr7:140037621
|
C | T | 12 | a0003c0004t0003g0016a0003c0004t0003g0018a0003c0004t0003g0019others(9): Show | 15 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1324+94G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037621 | ||||||
chr7:140037992
|
A | G | 12 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(9): Show | 13 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183-136T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140037992 | ||||||
chr7:140037998
|
T | C | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1183-142A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140037998 | ||||||
chr7:140038063
|
C | T | 3 | a0003c0004t0003g0017a0003c0004t0003g0065a0003c0004t0003g0066 | 4 | HG00735.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-207G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038063 | ||||||
chr7:140038096
|
A | C | 2 | a0001c0002t0001g0011a0001c0002t0001g0213 | 4 | NA18968.hp2 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-240T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038096 | ||||||
chr7:140038188
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1183-332G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038188 | ||||||
chr7:140038255
|
C | A | 2 | a0001c0001t0003g0134a0001c0001t0003g0185 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1183-399G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038255 | ||||||
chr7:140038567
|
A | G | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1183-711T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038567 | ||||||
chr7:140038707
|
A | C | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1183-851T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038707 | ||||||
chr7:140038761
|
T | C | 7 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(4): Show | 8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183-905A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038761 | ||||||
chr7:140038819
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1183-963C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038819 | ||||||
chr7:140039127
|
T | C | 3 | a0003c0004t0003g0017a0003c0004t0003g0065a0003c0004t0003g0066 | 4 | HG00735.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-1271A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039127 | ||||||
chr7:140039340
|
T | C | 1 | a0001c0002t0001g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1183-1484A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039340 | ||||||
chr7:140039392
|
G | T | 1 | a0001c0002t0001g0178 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1183-1536C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039392 | ||||||
chr7:140039625
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1183-1769G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039625 | ||||||
chr7:140039778
|
C | T | 16 | a0001c0002t0001g0009a0002c0005t0003g0160a0002c0005t0004g0044others(13): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+1866G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039778 | ||||||
chr7:140039863
|
C | T | 7 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(4): Show | 8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182+1781G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039863 | ||||||
chr7:140039887
|
A | ACTGCT | 16 | a0001c0002t0001g0009a0002c0005t0003g0160a0002c0005t0004g0044others(13): Show | 19 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+1752_1182+175 others(9): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039887 | ||||||
chr7:140040513
|
C | T | 45 | a0001c0001t0002g0008a0001c0001t0002g0013a0001c0001t0002g0014others(42): Show | 53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1182+1131G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040513 | ||||||
chr7:140040644
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0057 | 2 | NA18944.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1182+1000G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040644 | ||||||
chr7:140040786
|
T | C | 289 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(286): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1182+858A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040786 | ||||||
chr7:140040896
|
T | C | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+748A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040896 | ||||||
chr7:140040912
|
C | T | 2 | a0001c0009t0001g0267a0001c0009t0001g0273 | 2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1182+732G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040912 | ||||||
chr7:140041064
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1182+580C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041064 | ||||||
chr7:140041083
|
A | G | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+561T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041083 | ||||||
chr7:140041139
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1182+505A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041139 | ||||||
chr7:140041274
|
A | G | 15 | a0001c0002t0001g0261a0002c0005t0003g0160a0002c0005t0004g0044others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1182+370T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041274 | ||||||
chr7:140041306
|
T | C | 16 | a0001c0002t0001g0261a0002c0005t0003g0160a0002c0005t0004g0044others(13): Show | 17 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1182+338A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041306 | ||||||
chr7:140041430
|
C | T | 2 | a0001c0002t0001g0231a0001c0002t0001g0232 | 2 | HG01069.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1182+214G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041430 | ||||||
chr7:140041966
|
C | T | 37 | a0001c0001t0003g0134a0001c0001t0003g0185a0001c0001t0005g0168others(34): Show | 42 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.987-127G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140041966 | ||||||
chr7:140041986
|
C | T | 8 | a0001c0002t0001g0037a0001c0002t0001g0200a0001c0002t0001g0208others(5): Show | 9 | HG00423.hp2 HG02074.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.987-147G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140041986 | ||||||
chr7:140042347
|
G | A | 1 | a0002c0005t0004g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.987-508C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042347 | ||||||
chr7:140042510
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.987-671C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042510 | ||||||
chr7:140042669
|
G | A | 3 | a0001c0003t0003g0029a0001c0003t0003g0144a0001c0003t0003g0183 | 4 | HG01952.hp1 HG02257.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-830C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042669 | ||||||
chr7:140042853
|
A | G | 4 | a0001c0001t0002g0058a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG00741.hp1 HG01070.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-1014T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042853 | ||||||
chr7:140042898
|
C | T | 1 | a0002c0005t0004g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.987-1059G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042898 | ||||||
chr7:140042922
|
A | G | 10 | a0001c0002t0001g0006a0001c0002t0001g0012a0001c0002t0001g0157others(7): Show | 15 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.987-1083T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042922 | ||||||
chr7:140042923
|
T | C | 8 | a0001c0002t0001g0006a0001c0002t0001g0012a0001c0002t0001g0201others(5): Show | 13 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.987-1084A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042923 | ||||||
chr7:140042934
|
G | A | 1 | a0001c0013t0002g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.987-1095C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042934 | ||||||
chr7:140043039
|
C | CA | 3 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159 | 4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1201dupT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043039 | ||||||
chr7:140043050
|
C | T | 3 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159 | 4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1211G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043050 | ||||||
chr7:140043054
|
A | C | 3 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159 | 4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1215T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043054 | ||||||
chr7:140043111
|
A | G | 2 | a0001c0001t0002g0123a0001c0001t0002g0234 | 2 | HG02630.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.987-1272T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043111 | ||||||
chr7:140043173
|
G | A | 1 | a0001c0001t0002g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.987-1334C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043173 | ||||||
chr7:140043234
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.987-1395G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043234 | ||||||
chr7:140043249
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.987-1410C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043249 | ||||||
chr7:140043653
|
G | C | 1 | a0001c0002t0001g0167 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.987-1814C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043653 | ||||||
chr7:140043687
|
C | T | 8 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(5): Show | 9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.987-1848G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043687 | ||||||
chr7:140043704
|
T | C | 1 | a0002c0007t0003g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.987-1865A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043704 | ||||||
chr7:140043811
|
C | T | 1 | a0001c0001t0003g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987-1972G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043811 | ||||||
chr7:140043817
|
C | T | 1 | a0005c0011t0003g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.987-1978G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043817 | ||||||
chr7:140043883
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.987-2044C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043883 | ||||||
chr7:140043949
|
G | C | 3 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159 | 4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-2110C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043949 | ||||||
chr7:140043966
|
G | C | 1 | a0001c0001t0002g0234 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.987-2127C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043966 | ||||||
chr7:140044125
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.987-2286G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044125 | ||||||
chr7:140044335
|
C | T | 1 | a0001c0001t0002g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.987-2496G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044335 | ||||||
chr7:140044360
|
T | C | 11 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(8): Show | 13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.987-2521A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044360 | ||||||
chr7:140044367
|
T | C | 2 | a0003c0004t0003g0063a0003c0004t0003g0064 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.986+2517A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044367 | ||||||
chr7:140044397
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.986+2487T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044397 | ||||||
chr7:140044440
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.986+2444C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044440 | ||||||
chr7:140044906
|
T | C | 1 | a0001c0002t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.986+1978A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044906 | ||||||
chr7:140045002
|
T | G | 37 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(34): Show | 42 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.986+1882A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045002 | ||||||
chr7:140045006
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.986+1878G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045006 | ||||||
chr7:140045029
|
C | CT | 14 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(11): Show | 18 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.986+1854dupA | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045029 | ||||||
chr7:140045098
|
T | C | 4 | a0001c0002t0001g0166a0001c0002t0001g0237a0001c0002t0001g0262others(1): Show | 4 | NA18968.hp1 NA18973.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+1786A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045098 | ||||||
chr7:140045177
|
G | A | 2 | a0001c0002t0001g0213a0001c0002t0001g0214 | 2 | NA18974.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.986+1707C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045177 | ||||||
chr7:140045203
|
T | A | 1 | a0001c0001t0002g0105 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.986+1681A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045203 | ||||||
chr7:140045246
|
T | A | 2 | a0001c0002t0001g0166a0001c0002t0001g0274 | 2 | NA18973.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.986+1638A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045246 | ||||||
chr7:140045372
|
C | G | 15 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(12): Show | 16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.986+1512G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045372 | ||||||
chr7:140045548
|
T | C | 3 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159 | 4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+1336A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045548 | ||||||
chr7:140045800
|
C | T | 2 | a0001c0001t0002g0095a0001c0001t0002g0106 | 2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.986+1084G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045800 | ||||||
chr7:140045805
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.986+1079A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045805 | ||||||
chr7:140045983
|
TGAACGAT others(1): Show |
T | 6 | a0002c0005t0004g0278a0002c0005t0004g0279a0002c0005t0004g0280others(3): Show | 6 | HG01261.hp2 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.986+893_986+900del others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045983 | ||||||
chr7:140045991
|
G | A | 104 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(101): Show | 138 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.986+893C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045991 | ||||||
chr7:140046035
|
C | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.986+849G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046035 | ||||||
chr7:140046093
|
A | G | 22 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(19): Show | 23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.986+791T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046093 | ||||||
chr7:140046195
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.986+689A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046195 | ||||||
chr7:140046221
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.986+663T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046221 | ||||||
chr7:140046303
|
T | G | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.986+581A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046303 | ||||||
chr7:140046503
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.986+381G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046503 | ||||||
chr7:140046721
|
A | AGT | 8 | a0001c0001t0002g0050a0001c0001t0002g0060a0001c0001t0002g0081others(5): Show | 8 | HG00741.hp2 HG01884.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.986+161_986+162dup others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGT | 8 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(5): Show | 9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.986+159_986+162dup others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGTGTG others(1): Show |
5 | a0003c0004t0003g0017a0003c0004t0003g0065a0003c0004t0003g0066others(2): Show | 6 | HG00639.hp2 HG00735.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.986+155_986+162dup others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGTGTG others(3): Show |
2 | a0003c0004t0003g0071a0003c0004t0003g0072 | 2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.986+153_986+162dup others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGTGTG others(5): Show |
2 | a0003c0004t0003g0069a0003c0004t0003g0135 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.986+151_986+162dup others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGTGTG others(7): Show |
3 | a0003c0004t0003g0019a0003c0004t0003g0063a0003c0004t0003g0064 | 4 | HG04115.hp1 HG04204.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+149_986+162dup others(14): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGTGTG others(11): Show |
2 | a0003c0004t0003g0018a0003c0004t0003g0068 | 3 | HG01069.hp1 HG01071.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.986+145_986+162dup others(18): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
A | AGTGTGTG others(13): Show |
1 | a0003c0004t0003g0016 | 2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.986+143_986+162dup others(20): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
AGT | A | 72 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(69): Show | 79 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.986+161_986+162del others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
AGTGT | A | 131 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0077others(128): Show | 175 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.986+159_986+162del others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
AGTGTGT | A | 5 | a0001c0001t0002g0234a0001c0001t0003g0134a0001c0002t0001g0039others(2): Show | 6 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.986+157_986+162del others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046721
|
AGTGTGTG others(1): Show |
A | 3 | a0001c0002t0001g0206a0004c0010t0002g0124a0004c0010t0002g0174 | 3 | HG00140.hp2 HG01074.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.986+155_986+162del others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | ||||||
chr7:140046799
|
A | AGT | 16 | a0001c0001t0002g0015a0001c0001t0002g0023a0001c0001t0002g0024others(13): Show | 19 | HG00099.hp2 HG00438.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.986+83_986+84dupAC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGT | 19 | a0001c0001t0002g0089a0001c0001t0002g0142a0001c0001t0002g0175others(16): Show | 20 | HG00408.hp2 HG00639.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.986+81_986+84dupAC others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGT | 23 | a0001c0001t0003g0185a0001c0003t0001g0027a0001c0003t0001g0158others(20): Show | 27 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.986+79_986+84dupAC others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGTG others(1): Show |
5 | a0001c0003t0003g0073a0001c0003t0003g0074a0001c0003t0003g0137others(2): Show | 6 | HG00738.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.986+77_986+84dupAC others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGTG others(3): Show |
5 | a0001c0003t0003g0026a0001c0003t0003g0030a0001c0003t0003g0136others(2): Show | 7 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.986+75_986+84dupAC others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGTG others(5): Show |
1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.986+73_986+84dupAC others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGTG others(7): Show |
5 | a0001c0001t0003g0134a0002c0007t0003g0180a0002c0007t0004g0287others(2): Show | 5 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+71_986+84dupAC others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGTG others(9): Show |
1 | a0002c0007t0003g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.986+69_986+84dupAC others(14): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
A | AGTGTGTG others(11): Show |
1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.986+67_986+84dupAC others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046799
|
AGTGT | A | 4 | a0001c0001t0002g0057a0001c0001t0002g0184a0001c0002t0001g0042others(1): Show | 5 | HG01891.hp2 HG04184.hp2 NA19086.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+81_986+84delAC others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | ||||||
chr7:140046832
|
G | C | 2 | a0001c0002t0001g0042a0001c0002t0001g0251 | 3 | HG01891.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.986+52C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046832 | ||||||
chr7:140046833
|
T | A | 2 | a0001c0002t0001g0042a0001c0002t0001g0251 | 3 | HG01891.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.986+51A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTCA | 5 | a0001c0002t0001g0037a0001c0002t0001g0189a0001c0002t0001g0218others(2): Show | 6 | HG00423.hp2 HG01243.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTGTCA | 9 | a0001c0002t0001g0028a0001c0002t0001g0041a0001c0002t0001g0045others(6): Show | 12 | HG01952.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTGTGTC others(1): Show |
13 | a0001c0001t0002g0244a0001c0002t0001g0009a0001c0002t0001g0165others(10): Show | 20 | HG00099.hp1 HG00673.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTGTGTG others(3): Show |
20 | a0001c0002t0001g0033a0001c0002t0001g0040a0001c0002t0001g0166others(17): Show | 22 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTGTGTG others(5): Show |
40 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(37): Show | 58 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTGTGTG others(7): Show |
17 | a0001c0002t0001g0012a0001c0002t0001g0036a0001c0002t0001g0039others(14): Show | 21 | HG00408.hp1 HG01069.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140046833
|
T | TGTGTGTG others(11): Show |
2 | a0001c0002t0001g0221a0001c0002t0001g0256 | 2 | HG02258.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.986+50_986+51insTG others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | ||||||
chr7:140047123
|
G | A | 2 | a0001c0001t0005g0169a0001c0001t0005g0171 | 2 | HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.863-116C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047123 | ||||||
chr7:140047215
|
T | C | 1 | a0002c0005t0004g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.863-208A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047215 | ||||||
chr7:140047319
|
G | A | 1 | a0001c0002t0012g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.863-312C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047319 | ||||||
chr7:140047334
|
C | T | 1 | a0001c0001t0007g0088 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.863-327G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047334 | ||||||
chr7:140047349
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.863-342C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047349 | ||||||
chr7:140047500
|
C | T | 12 | a0001c0003t0003g0026a0001c0003t0003g0030a0001c0003t0003g0073others(9): Show | 14 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.863-493G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047500 | ||||||
chr7:140047502
|
T | C | 1 | a0001c0001t0002g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.863-495A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047502 | ||||||
chr7:140047622
|
C | A | 2 | a0001c0002t0001g0220a0001c0002t0001g0225 | 2 | NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.863-615G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047622 | ||||||
chr7:140047674
|
G | A | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.863-667C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047674 | ||||||
chr7:140047768
|
C | A | 2 | a0002c0005t0004g0284a0002c0005t0004g0285 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.863-761G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047768 | ||||||
chr7:140048194
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.863-1187T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048194 | ||||||
chr7:140048201
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.863-1194G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048201 | ||||||
chr7:140048258
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.863-1251G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048258 | ||||||
chr7:140048411
|
G | A | 2 | a0001c0001t0003g0134a0001c0001t0003g0185 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.863-1404C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048411 | ||||||
chr7:140048531
|
T | C | 1 | a0001c0001t0002g0107 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.863-1524A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048531 | ||||||
chr7:140048939
|
C | G | 169 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(166): Show | 214 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.863-1932G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048939 | ||||||
chr7:140048992
|
T | C | 1 | a0003c0004t0003g0017 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.863-1985A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048992 | ||||||
chr7:140049110
|
TG | T | 11 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(8): Show | 13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.863-2104delC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049110 | ||||||
chr7:140049159
|
T | C | 22 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(19): Show | 23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-2152A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049159 | ||||||
chr7:140049249
|
C | T | 22 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(19): Show | 23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-2242G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049249 | ||||||
chr7:140049250
|
C | G | 1 | a0001c0003t0003g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.863-2243G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049250 | ||||||
chr7:140049258
|
G | T | 169 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(166): Show | 214 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.863-2251C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049258 | ||||||
chr7:140049471
|
G | C | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0121 | 3 | HG00438.hp1 NA18959.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.863-2464C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049471 | ||||||
chr7:140049546
|
G | A | 105 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0007others(102): Show | 140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.863-2539C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049546 | ||||||
chr7:140049814
|
A | G | 4 | a0001c0002t0001g0178a0001c0002t0001g0179a0001c0002t0001g0243others(1): Show | 4 | HG00673.hp2 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-2807T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049814 | ||||||
chr7:140049918
|
T | G | 1 | a0001c0002t0001g0232 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.863-2911A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049918 | ||||||
chr7:140049992
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.863-2985G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049992 | ||||||
chr7:140049993
|
C | T | 2 | a0001c0009t0001g0264a0001c0009t0001g0271 | 2 | HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.863-2986G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049993 | ||||||
chr7:140050148
|
G | A | 3 | a0001c0002t0001g0229a0001c0002t0001g0269a0001c0002t0001g0270 | 3 | HG00673.hp1 NA18971.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.863-3141C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140050148 | ||||||
chr7:140050185
|
C | G | 1 | a0001c0002t0001g0242 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.863-3178G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140050185 | ||||||
chr7:140050644
|
G | A | 1 | a0001c0009t0001g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.863-3637C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140050644 | ||||||
chr7:140051159
|
T | C | 1 | a0001c0001t0002g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.862+3503A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051159 | ||||||
chr7:140051198
|
G | A | 11 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(8): Show | 13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+3464C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051198 | ||||||
chr7:140051205
|
A | G | 2 | a0005c0011t0003g0188a0005c0011t0003g0191 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.862+3457T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051205 | ||||||
chr7:140051217
|
T | C | 11 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(8): Show | 13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+3445A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051217 | ||||||
chr7:140051270
|
A | G | 2 | a0002c0005t0004g0044a0002c0005t0004g0281 | 3 | HG03041.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.862+3392T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051270 | ||||||
chr7:140051423
|
C | T | 1 | a0001c0002t0001g0255 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.862+3239G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051423 | ||||||
chr7:140051430
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0133 | 3 | HG03491.hp2 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.862+3232C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051430 | ||||||
chr7:140051448
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.862+3214A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051448 | ||||||
chr7:140051552
|
A | G | 170 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(167): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.862+3110T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051552 | ||||||
chr7:140051580
|
A | G | 22 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(19): Show | 23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.862+3082T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051580 | ||||||
chr7:140051603
|
C | T | 2 | a0001c0001t0002g0052a0001c0001t0002g0085 | 2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.862+3059G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051603 | ||||||
chr7:140051643
|
G | A | 1 | a0001c0001t0003g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.862+3019C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051643 | ||||||
chr7:140051861
|
T | C | 8 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(5): Show | 9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.862+2801A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051861 | ||||||
chr7:140051922
|
T | C | 1 | a0007c0016t0003g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.862+2740A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051922 | ||||||
chr7:140052387
|
A | C | 1 | a0001c0002t0001g0207 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.862+2275T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052387 | ||||||
chr7:140052521
|
T | C | 1 | a0002c0005t0004g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.862+2141A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052521 | ||||||
chr7:140052672
|
GAACTCCA others(3): Show |
G | 2 | a0001c0002t0001g0240a0001c0002t0001g0241 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.862+1980_862+1989d others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052672 | ||||||
chr7:140052732
|
T | G | 1 | a0001c0001t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.862+1930A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
T | TGTG | 3 | a0001c0002t0001g0220a0001c0002t0001g0253a0001c0002t0001g0254 | 3 | HG03471.hp1 HG03471.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.862+1929_862+1930i others(5): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
T | TTG | 29 | a0001c0001t0002g0023a0001c0001t0002g0047a0001c0001t0002g0111others(26): Show | 36 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.862+1928_862+1929d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
T | TTGTG | 95 | a0001c0001t0002g0024a0001c0001t0002g0059a0001c0001t0002g0118others(92): Show | 128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.862+1926_862+1929d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
T | TTGTGTG | 21 | a0001c0001t0002g0122a0001c0002t0001g0010a0001c0002t0001g0179others(18): Show | 23 | HG00639.hp1 HG01167.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.862+1924_862+1929d others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
T | TTGTGTGT others(1): Show |
4 | a0001c0002t0001g0011a0001c0002t0001g0166a0001c0002t0001g0263others(1): Show | 6 | HG03130.hp2 NA18968.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+1922_862+1929d others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
T | TTGTGTGT others(3): Show |
1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.862+1920_862+1929d others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
TTG | T | 11 | a0001c0001t0002g0079a0001c0001t0002g0141a0001c0001t0003g0185others(8): Show | 11 | HG01123.hp2 HG02273.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.862+1928_862+1929d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
TTGTG | T | 5 | a0001c0001t0002g0021a0001c0001t0002g0084a0001c0001t0002g0184others(2): Show | 6 | HG01261.hp2 HG02083.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+1926_862+1929d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140052732
|
TTGTGTG | T | 12 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(9): Show | 13 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.862+1924_862+1929d others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | ||||||
chr7:140053090
|
T | TAA | 172 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0003g0134others(169): Show | 217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.862+1571_862+1572i others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053090 | ||||||
chr7:140053172
|
G | T | 1 | a0001c0002t0001g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.862+1490C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053172 | ||||||
chr7:140053280
|
T | C | 172 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0003g0134others(169): Show | 217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.862+1382A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053280 | ||||||
chr7:140053631
|
G | A | 172 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0003g0134others(169): Show | 217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.862+1031C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053631 | ||||||
chr7:140053801
|
A | T | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.862+861T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053801 | ||||||
chr7:140053805
|
T | C | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.862+857A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053805 | ||||||
chr7:140053899
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.862+763C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053899 | ||||||
chr7:140053953
|
A | C | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.862+709T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053953 | ||||||
chr7:140054096
|
A | G | 1 | a0007c0016t0003g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.862+566T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054096 | ||||||
chr7:140054140
|
G | C | 289 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(286): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.862+522C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054140 | ||||||
chr7:140054219
|
C | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.862+443G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054219 | ||||||
chr7:140054322
|
C | T | 2 | a0001c0002t0001g0231a0001c0002t0001g0232 | 2 | HG01069.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.862+340G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054322 | ||||||
chr7:140054473
|
T | C | 7 | a0002c0007t0003g0180a0002c0007t0003g0181a0002c0007t0003g0187others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+189A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054473 | ||||||
chr7:140054646
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.862+16C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054646 | ||||||
chr7:140054651
|
T | C | 170 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(167): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.862+11A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054651 | ||||||
chr7:140054885
|
G | A | 11 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(8): Show | 13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-122C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140054885 | ||||||
chr7:140055019
|
T | C | 170 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(167): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.761-256A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055019 | ||||||
chr7:140055149
|
C | G | 1 | a0002c0007t0013g0288 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.761-386G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055149 | ||||||
chr7:140055179
|
T | A | 11 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(8): Show | 13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-416A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055179 | ||||||
chr7:140055194
|
A | C | 1 | a0001c0001t0002g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.761-431T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055194 | ||||||
chr7:140055372
|
T | A | 1 | a0001c0001t0003g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.761-609A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055372 | ||||||
chr7:140055504
|
A | C | 22 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(19): Show | 23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.761-741T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055504 | ||||||
chr7:140055507
|
C | T | 1 | a0001c0008t0002g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.761-744G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055507 | ||||||
chr7:140055597
|
C | T | 1 | a0001c0003t0003g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.761-834G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055597 | ||||||
chr7:140055624
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.761-861G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055624 | ||||||
chr7:140055629
|
G | A | 1 | a0010c0017t0003g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.761-866C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055629 | ||||||
chr7:140055698
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.761-935T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055698 | ||||||
chr7:140055726
|
A | G | 3 | a0003c0004t0003g0067a0003c0004t0003g0071a0003c0004t0003g0072 | 3 | HG02698.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.761-963T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055726 | ||||||
chr7:140055859
|
C | A | 1 | a0001c0006t0001g0226 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.760+997G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055859 | ||||||
chr7:140056045
|
A | G | 4 | a0001c0001t0002g0008a0001c0001t0002g0079a0001c0001t0002g0080others(1): Show | 6 | HG01346.hp1 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.760+811T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056045 | ||||||
chr7:140056378
|
T | C | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.760+478A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056378 | ||||||
chr7:140056434
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.760+422A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056434 | ||||||
chr7:140056545
|
T | G | 8 | a0001c0003t0003g0026a0001c0003t0003g0073a0001c0003t0003g0074others(5): Show | 9 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.760+311A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056545 | ||||||
chr7:140056658
|
A | T | 172 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0003g0134others(169): Show | 217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.760+198T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056658 | ||||||
chr7:140056675
|
T | G | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+181A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056675 | ||||||
chr7:140056677
|
T | A | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+179A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056677 | ||||||
chr7:140056679
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+177G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056679 | ||||||
chr7:140056681
|
C | G | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+175G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056681 | ||||||
chr7:140056682
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+174T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056682 | ||||||
chr7:140056684
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+172G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056684 | ||||||
chr7:140056686
|
C | G | 2 | a0001c0008t0002g0020a0001c0008t0002g0049 | 3 | HG01192.hp2 HG03490.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.760+170G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056686 | ||||||
chr7:140056687
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+169G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056687 | ||||||
chr7:140056688
|
G | C | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+168C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056688 | ||||||
chr7:140056698
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+158G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056698 | ||||||
chr7:140056700
|
TTGTTAGG others(3): Show |
T | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+146_760+155del others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056700 | ||||||
chr7:140056716
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+140T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056716 | ||||||
chr7:140057201
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.463-48C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057201 | ||||||
chr7:140057271
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.463-118T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057271 | ||||||
chr7:140057336
|
G | T | 155 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(152): Show | 196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.463-183C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057336 | ||||||
chr7:140057375
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463-222G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057375 | ||||||
chr7:140057498
|
CTCA | C | 20 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(17): Show | 21 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.463-348_463-346del others(3): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057498 | ||||||
chr7:140057816
|
A | T | 1 | a0001c0001t0002g0145 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.462+83T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057816 | ||||||
chr7:140058111
|
C | G | 36 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(33): Show | 41 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.327-77G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058111 | ||||||
chr7:140058111
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.327-77G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058111 | ||||||
chr7:140058180
|
T | C | 29 | a0001c0002t0001g0007a0001c0002t0001g0038a0001c0002t0001g0167others(26): Show | 34 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.327-146A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058180 | ||||||
chr7:140058196
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.327-162G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058196 | ||||||
chr7:140058253
|
C | T | 170 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(167): Show | 215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.327-219G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058253 | ||||||
chr7:140058294
|
G | A | 9 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(6): Show | 10 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-260C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058294 | ||||||
chr7:140058336
|
C | T | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.327-302G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058336 | ||||||
chr7:140058355
|
T | C | 9 | a0003c0004t0003g0018a0003c0004t0003g0019a0003c0004t0003g0067others(6): Show | 11 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-321A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058355 | ||||||
chr7:140058389
|
T | C | 1 | a0001c0002t0001g0230 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.327-355A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058389 | ||||||
chr7:140058395
|
C | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.327-361G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058395 | ||||||
chr7:140058416
|
C | A | 1 | a0001c0001t0002g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.327-382G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058416 | ||||||
chr7:140058435
|
C | T | 1 | a0002c0007t0003g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327-401G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058435 | ||||||
chr7:140058492
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327-458A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058492 | ||||||
chr7:140058575
|
G | A | 20 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(17): Show | 21 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-541C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058575 | ||||||
chr7:140058619
|
C | T | 1 | a0005c0011t0003g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-585G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058619 | ||||||
chr7:140058629
|
G | C | 1 | a0001c0001t0005g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.327-595C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058629 | ||||||
chr7:140058676
|
C | T | 155 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(152): Show | 196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.327-642G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058676 | ||||||
chr7:140058792
|
A | G | 1 | a0001c0002t0001g0038 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.327-758T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058792 | ||||||
chr7:140058815
|
G | C | 121 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(118): Show | 159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.327-781C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058815 | ||||||
chr7:140058885
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.327-851G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058885 | ||||||
chr7:140058894
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.327-860C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058894 | ||||||
chr7:140058921
|
A | C | 155 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(152): Show | 196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.327-887T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058921 | ||||||
chr7:140058929
|
C | A | 1 | a0001c0001t0002g0126 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.327-895G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058929 | ||||||
chr7:140058959
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.327-925C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058959 | ||||||
chr7:140059026
|
C | T | 123 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(120): Show | 161 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.327-992G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059026 | ||||||
chr7:140059083
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.327-1049C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059083 | ||||||
chr7:140059088
|
T | A | 2 | a0001c0002t0001g0231a0001c0002t0001g0232 | 2 | HG01069.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.327-1054A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059088 | ||||||
chr7:140059261
|
T | C | 1 | a0002c0005t0004g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.327-1227A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059261 | ||||||
chr7:140059355
|
C | T | 1 | a0001c0001t0005g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.327-1321G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059355 | ||||||
chr7:140059361
|
T | TAC | 16 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(13): Show | 17 | HG01243.hp1 HG01346.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.327-1329_327-1328d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | ||||||
chr7:140059361
|
T | TACAC | 12 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(9): Show | 13 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-1331_327-1328d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | ||||||
chr7:140059361
|
TAC | T | 105 | a0001c0001t0002g0244a0001c0001t0003g0134a0001c0002t0001g0004others(102): Show | 140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.327-1329_327-1328d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | ||||||
chr7:140059361
|
TACACACA others(1): Show |
T | 13 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(10): Show | 15 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.327-1335_327-1328d others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | ||||||
chr7:140059363
|
C | T | 1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327-1329G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059363 | ||||||
chr7:140059402
|
C | CTCT | 112 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(109): Show | 148 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.327-1369_327-1368i others(5): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059402 | ||||||
chr7:140059402
|
C | CTCTT | 36 | a0001c0001t0002g0175a0001c0001t0003g0134a0001c0001t0003g0185others(33): Show | 43 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.327-1369_327-1368i others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059402 | ||||||
chr7:140059402
|
C | CTCTTT | 24 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159others(21): Show | 26 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-1369_327-1368i others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059402 | ||||||
chr7:140059534
|
G | A | 4 | a0001c0001t0002g0025a0001c0001t0002g0131a0001c0001t0002g0132others(1): Show | 5 | HG02451.hp2 HG02559.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-1500C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059534 | ||||||
chr7:140059778
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.327-1744C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059778 | ||||||
chr7:140059795
|
G | A | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.327-1761C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059795 | ||||||
chr7:140059820
|
C | T | 5 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(2): Show | 5 | HG01123.hp2 HG01361.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-1786G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059820 | ||||||
chr7:140059827
|
C | T | 21 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(18): Show | 22 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.327-1793G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059827 | ||||||
chr7:140059930
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.327-1896C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059930 | ||||||
chr7:140060202
|
C | T | 121 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(118): Show | 159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.327-2168G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060202 | ||||||
chr7:140060210
|
T | C | 172 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0003g0134others(169): Show | 217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.327-2176A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060210 | ||||||
chr7:140060491
|
T | C | 1 | a0001c0002t0001g0011 | 3 | NA18968.hp2 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.326+2031A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060491 | ||||||
chr7:140060538
|
G | C | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.326+1984C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060538 | ||||||
chr7:140060740
|
TCCCTGCT others(3): Show |
T | 122 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(119): Show | 160 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.326+1772_326+1781d others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060740 | ||||||
chr7:140060849
|
G | C | 1 | a0001c0001t0002g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.326+1673C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060849 | ||||||
chr7:140060855
|
C | T | 1 | a0002c0007t0003g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.326+1667G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060855 | ||||||
chr7:140060898
|
C | G | 3 | a0001c0003t0001g0027a0001c0003t0001g0158a0001c0003t0001g0159 | 4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+1624G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060898 | ||||||
chr7:140060987
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+1535G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060987 | ||||||
chr7:140061202
|
T | G | 15 | a0003c0004t0003g0016a0003c0004t0003g0017a0003c0004t0003g0018others(12): Show | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.326+1320A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061202 | ||||||
chr7:140061326
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.326+1196A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061326 | ||||||
chr7:140061341
|
G | A | 8 | a0001c0001t0002g0175a0001c0001t0005g0168a0001c0001t0005g0169others(5): Show | 9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+1181C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061341 | ||||||
chr7:140061360
|
T | A | 11 | a0002c0007t0003g0180a0002c0007t0003g0181a0002c0007t0003g0187others(8): Show | 11 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+1162A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061360 | ||||||
chr7:140061376
|
T | A | 121 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(118): Show | 159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.326+1146A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061376 | ||||||
chr7:140061448
|
A | G | 105 | a0001c0001t0002g0244a0001c0002t0001g0004a0001c0002t0001g0006others(102): Show | 140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.326+1074T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061448 | ||||||
chr7:140061452
|
T | TACAC | 11 | a0002c0005t0003g0160a0002c0005t0004g0044a0002c0005t0004g0278others(8): Show | 12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.326+1066_326+1069d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061452 | ||||||
chr7:140061568
|
G | T | 1 | a0001c0002t0001g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.326+954C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061568 | ||||||
chr7:140061663
|
C | T | 150 | a0001c0001t0002g0175a0001c0001t0002g0244a0001c0001t0005g0168others(147): Show | 191 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.326+859G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061663 | ||||||
chr7:140061699
|
C | A | 2 | a0003c0004t0003g0071a0003c0004t0003g0072 | 2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.326+823G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061699 | ||||||
chr7:140061842
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.326+680A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061842 | ||||||
chr7:140061871
|
GT | G | 12 | a0001c0003t0003g0026a0001c0003t0003g0030a0001c0003t0003g0073others(9): Show | 14 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+650delA | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061871 | ||||||
chr7:140061983
|
CG | C | 144 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0013others(141): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.326+538delC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061983 | ||||||
chr7:140061983
|
CGG | C | 70 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143others(67): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.326+537_326+538del others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061983 | ||||||
chr7:140061986
|
G | C | 1 | a0001c0002t0001g0274 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.326+536C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061986 | ||||||
chr7:140061989
|
G | A | 1 | a0001c0002t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.326+533C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061989 | ||||||
chr7:140061993
|
G | C | 1 | a0008c0015t0009g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.326+529C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061993 | ||||||
chr7:140061994
|
G | GA | 4 | a0001c0003t0003g0030a0001c0003t0003g0193a0001c0003t0003g0194others(1): Show | 5 | HG01884.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.326+527_326+528ins others(1): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061994 | ||||||
chr7:140062046
|
A | G | 1 | a0001c0001t0002g0014 | 2 | NA18975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.326+476T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062046 | ||||||
chr7:140062096
|
T | A | 169 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0145others(166): Show | 218 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.326+426A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062096 | ||||||
chr7:140062318
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0046a0001c0001t0002g0047others(1): Show | 5 | NA18962.hp1 NA19003.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.326+204G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062318 | ||||||
chr7:140062402
|
G | A | 7 | a0002c0007t0003g0180a0002c0007t0003g0181a0002c0007t0004g0287others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+120C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062402 | ||||||
chr7:140062432
|
C | G | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+90G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062432 | ||||||
chr7:140062462
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.326+60C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062462 | ||||||
chr7:140062471
|
T | TG | 7 | a0002c0007t0003g0180a0002c0007t0003g0181a0002c0007t0004g0287others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+50dupC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062471 | ||||||
chr7:140062473
|
A | G | 188 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(185): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.326+49T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062473 | ||||||
chr7:140062477
|
C | G | 7 | a0002c0007t0003g0180a0002c0007t0003g0181a0002c0007t0004g0287others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+45G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062477 | ||||||
chr7:140062482
|
A | G | 168 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0005others(165): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.326+40T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062482 |