geneid | 55665 |
---|---|
ensemblid | ENSG00000106608.17 |
hgncid | 30890 |
symbol | URGCP |
name | upregulator of cell proliferation |
refseq_nuc | NM_001077663.3 |
refseq_prot | NP_001071131.1 |
ensembl_nuc | ENST00000453200.6 |
ensembl_prot | ENSP00000396918.1 |
mane_status | MANE Select |
chr | chr7 |
start | 43875913 |
end | 43906596 |
strand | - |
ver | v1.2 |
region | chr7:43875913-43906596 |
region5000 | chr7:43870913-43911596 |
regionname0 | URGCP_chr7_43875913_43906596 |
regionname5000 | URGCP_chr7_43870913_43911596 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 931 | 225 | 50 | 41 | 101 | 14 | 18 | 86 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002 | 0/1 | 931 | 170 | 42 | 35 | 75 | 4 | 13 | 55 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0003 | 0/0 | 931 | 3 | 0 | 0 | 1 | 0 | 2 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0004 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0005 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0006 | 0/0 | 931 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0007 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0008 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0009 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2796 | 160 | 34 | 35 | 75 | 4 | 11 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0002 | 1/0 | 2796 | 120 | 19 | 20 | 63 | 6 | 11 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0003 | 0/0 | 2796 | 54 | 8 | 8 | 37 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0004 | 0/0 | 2796 | 29 | 3 | 11 | 1 | 7 | 7 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0005 | 0/0 | 2796 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0006 | 0/0 | 2796 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0007 | 0/0 | 2796 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0008 | 0/0 | 2796 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0009 | 0/0 | 2796 | 3 | 2 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0010 | 0/0 | 2796 | 3 | 0 | 0 | 1 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0011 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0012 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0013 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0014 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0015 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0016 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0017 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0018 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0019 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0020 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
c0021 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 778 | 202 | 46 | 41 | 81 | 11 | 22 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0002 | 1/0 | 776 | 118 | 16 | 21 | 63 | 6 | 11 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0003 | 0/0 | 778 | 45 | 11 | 1 | 33 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0004 | 0/0 | 778 | 16 | 15 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0005 | 0/0 | 778 | 11 | 0 | 7 | 3 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0006 | 0/0 | 778 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0007 | 0/0 | 778 | 4 | 0 | 4 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0008 | 0/0 | 778 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0009 | 0/0 | 778 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
t0010 | 0/0 | 778 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 0 | 2 | 10 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0002 | 0/0 | 10 | 1 | 0 | 7 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0009 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 2796 | 120 | 19 | 20 | 63 | 6 | 11 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0003 | 0/0 | 2796 | 54 | 8 | 8 | 37 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0004 | 0/0 | 2796 | 29 | 3 | 11 | 1 | 7 | 7 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0005 | 0/0 | 2796 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0007 | 0/0 | 2796 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0008 | 0/0 | 2796 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0009 | 0/0 | 2796 | 3 | 2 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0017 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0018 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0019 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0001 | 0/1 | 2796 | 160 | 34 | 35 | 75 | 4 | 11 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0006 | 0/0 | 2796 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0013 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0020 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0003c0010 | 0/0 | 2796 | 3 | 0 | 0 | 1 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0004c0014 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0005c0012 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0006c0016 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0007c0015 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0008c0021 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0009c0011 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 1/0 | 3571 | 117 | 16 | 20 | 63 | 6 | 11 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0002t0006 | 0/0 | 3573 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0002t0010 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0003t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0003t0003 | 0/0 | 3573 | 36 | 2 | 1 | 33 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0003t0004 | 0/0 | 3573 | 6 | 6 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0003t0005 | 0/0 | 3573 | 11 | 0 | 7 | 3 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0004t0001 | 0/0 | 3573 | 29 | 3 | 11 | 1 | 7 | 7 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0005t0003 | 0/0 | 3573 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0007t0004 | 0/0 | 3573 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0008t0006 | 0/0 | 3573 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0009t0004 | 0/0 | 3573 | 3 | 2 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0017t0004 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0018t0003 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0001c0019t0002 | 0/0 | 3571 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0001t0001 | 0/1 | 3573 | 154 | 34 | 30 | 75 | 4 | 10 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0001t0007 | 0/0 | 3573 | 4 | 0 | 4 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0001t0008 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0001t0009 | 0/0 | 3573 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0006t0001 | 0/0 | 3573 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0013t0001 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0002c0020t0001 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0003c0010t0001 | 0/0 | 3573 | 3 | 0 | 0 | 1 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0004c0014t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0005c0012t0001 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0006c0016t0001 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0007c0015t0004 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0008c0021t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
a0009c0011t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | copy fasta | chr7 | 43870913 | 43911596 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0002 | 0/0 | 10 | 1 | 0 | 7 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0003 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0002t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0003t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0005t0003g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0005t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0005t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0005t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0007t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0007t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0007t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0008t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0008t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0008t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0009t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0009t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0009t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0017t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0018t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0001c0019t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0001 | 0/0 | 14 | 0 | 2 | 10 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0007g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0001t0009g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0006t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0006t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0013t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0002c0020t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0003c0010t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0003c0010t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0003c0010t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0004c0014t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0005c0012t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0006c0016t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0007c0015t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0008c0021t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
a0009c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0250 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0199 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0101 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00140 | hp2 | a0001 | c0004 | t0001 | g0100 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0016 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00280 | hp2 | a0002 | c0001 | t0001 | g0009 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0189 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00323 | hp2 | a0001 | c0003 | t0005 | g0078 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0187 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0269 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00438 | hp2 | a0003 | c0010 | t0001 | g0264 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0069 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00597 | hp2 | a0001 | c0003 | t0003 | g0212 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0234 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0133 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0082 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00642 | hp1 | a0002 | c0001 | t0007 | g0041 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00642 | hp2 | a0001 | c0003 | t0005 | g0075 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0267 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0044 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00738 | hp1 | a0002 | c0001 | t0001 | g0125 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00741 | hp1 | a0001 | c0019 | t0002 | g0174 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG00741 | hp2 | a0001 | c0009 | t0004 | g0084 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01069 | hp1 | a0001 | c0003 | t0005 | g0080 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01069 | hp2 | a0002 | c0001 | t0001 | g0040 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01071 | hp1 | a0001 | c0003 | t0005 | g0024 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01074 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01081 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01106 | hp1 | a0002 | c0001 | t0007 | g0258 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01106 | hp2 | a0001 | c0004 | t0001 | g0046 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01109 | hp1 | a0001 | c0003 | t0003 | g0053 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01109 | hp2 | a0002 | c0001 | t0007 | g0041 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0171 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01167 | hp2 | a0001 | c0003 | t0005 | g0076 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01168 | hp1 | a0001 | c0003 | t0005 | g0081 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0237 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01175 | hp2 | a0002 | c0001 | t0007 | g0244 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01192 | hp1 | a0001 | c0003 | t0005 | g0024 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0040 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0302 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01243 | hp2 | a0002 | c0001 | t0001 | g0124 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0118 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01256 | hp1 | a0002 | c0001 | t0001 | g0012 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0048 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01257 | hp2 | a0001 | c0004 | t0001 | g0094 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01258 | hp1 | a0001 | c0004 | t0001 | g0025 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01258 | hp2 | a0001 | c0004 | t0001 | g0047 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0042 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01261 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0241 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0130 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01358 | hp1 | a0002 | c0001 | t0009 | g0278 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01358 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0239 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01433 | hp1 | a0002 | c0001 | t0001 | g0070 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0106 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0191 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0105 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01516 | hp1 | a0001 | c0004 | t0001 | g0092 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0207 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0190 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01517 | hp2 | a0001 | c0004 | t0001 | g0093 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01884 | hp1 | a0001 | c0005 | t0003 | g0219 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01884 | hp2 | a0002 | c0001 | t0001 | g0043 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01891 | hp1 | a0001 | c0007 | t0004 | g0014 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0103 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01928 | hp1 | a0002 | c0001 | t0001 | g0011 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01943 | hp1 | a0002 | c0001 | t0001 | g0275 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0018 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01978 | hp1 | a0002 | c0001 | t0001 | g0127 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01981 | hp1 | a0001 | c0003 | t0005 | g0079 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01981 | hp2 | a0002 | c0001 | t0001 | g0068 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0023 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02004 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0257 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02015 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0289 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0287 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02055 | hp1 | a0001 | c0018 | t0003 | g0218 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02055 | hp2 | a0001 | c0002 | t0010 | g0135 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0261 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02071 | hp2 | a0002 | c0001 | t0001 | g0054 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0285 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0210 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0268 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02080 | hp2 | a0001 | c0003 | t0005 | g0077 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0036 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02135 | hp1 | a0001 | c0003 | t0005 | g0160 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02145 | hp1 | a0002 | c0001 | t0001 | g0259 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02145 | hp2 | a0002 | c0006 | t0001 | g0026 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02257 | hp1 | a0001 | c0007 | t0004 | g0137 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0071 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02258 | hp1 | a0001 | c0008 | t0006 | g0089 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02258 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0151 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02280 | hp2 | a0002 | c0006 | t0001 | g0111 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02293 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0104 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0208 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0194 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02523 | hp1 | a0002 | c0001 | t0001 | g0286 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0066 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02572 | hp1 | a0002 | c0001 | t0001 | g0116 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02572 | hp2 | a0001 | c0007 | t0004 | g0014 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0149 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02602 | hp2 | a0001 | c0004 | t0001 | g0096 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02615 | hp2 | a0002 | c0001 | t0001 | g0129 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02622 | hp1 | a0002 | c0001 | t0001 | g0126 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02622 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02630 | hp2 | a0002 | c0001 | t0001 | g0296 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02647 | hp1 | a0002 | c0001 | t0001 | g0295 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0009 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02717 | hp1 | a0002 | c0006 | t0001 | g0108 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02717 | hp2 | a0001 | c0009 | t0004 | g0083 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02723 | hp1 | a0002 | c0001 | t0001 | g0294 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02723 | hp2 | a0002 | c0006 | t0001 | g0110 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02735 | hp1 | a0001 | c0004 | t0001 | g0045 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0033 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02738 | hp1 | a0002 | c0020 | t0001 | g0262 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0158 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02809 | hp1 | a0002 | c0001 | t0001 | g0119 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02809 | hp2 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02818 | hp1 | a0002 | c0001 | t0001 | g0021 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02818 | hp2 | a0002 | c0001 | t0001 | g0297 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02886 | hp1 | a0002 | c0001 | t0001 | g0121 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02895 | hp1 | a0002 | c0006 | t0001 | g0027 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0090 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02896 | hp1 | a0002 | c0001 | t0001 | g0031 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02896 | hp2 | a0002 | c0001 | t0001 | g0043 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02897 | hp1 | a0002 | c0006 | t0001 | g0027 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02897 | hp2 | a0002 | c0001 | t0001 | g0031 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02922 | hp1 | a0002 | c0001 | t0001 | g0030 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02922 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02965 | hp1 | a0001 | c0002 | t0006 | g0073 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02965 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0300 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0152 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03041 | hp1 | a0002 | c0001 | t0001 | g0122 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03041 | hp2 | a0002 | c0006 | t0001 | g0109 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03098 | hp1 | a0002 | c0001 | t0001 | g0293 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03139 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0195 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0091 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03195 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03209 | hp1 | a0001 | c0003 | t0003 | g0223 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03209 | hp2 | a0001 | c0003 | t0004 | g0305 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0235 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0279 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03486 | hp2 | a0001 | c0005 | t0003 | g0213 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0236 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03516 | hp2 | a0002 | c0001 | t0001 | g0117 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03540 | hp1 | a0002 | c0001 | t0001 | g0021 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03540 | hp2 | a0002 | c0001 | t0001 | g0299 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03579 | hp1 | a0001 | c0005 | t0003 | g0222 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03654 | hp1 | a0001 | c0004 | t0001 | g0025 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03654 | hp2 | a0001 | c0004 | t0001 | g0018 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03669 | hp1 | a0002 | c0001 | t0001 | g0012 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03669 | hp2 | a0002 | c0001 | t0001 | g0128 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0095 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0172 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03704 | hp1 | a0003 | c0010 | t0001 | g0256 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03704 | hp2 | a0002 | c0001 | t0001 | g0114 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03831 | hp2 | a0002 | c0013 | t0001 | g0266 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03834 | hp1 | a0001 | c0004 | t0001 | g0097 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0246 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03927 | hp2 | a0002 | c0001 | t0001 | g0055 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03942 | hp1 | a0003 | c0010 | t0001 | g0255 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03942 | hp2 | a0001 | c0004 | t0001 | g0099 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG04115 | hp2 | a0006 | c0016 | t0001 | g0273 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG04184 | hp1 | a0002 | c0001 | t0008 | g0263 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18522 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18522 | hp2 | a0002 | c0001 | t0001 | g0298 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0063 | EAS | CHB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | CHB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18906 | hp1 | a0002 | c0006 | t0001 | g0026 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18941 | hp2 | a0002 | c0001 | t0001 | g0271 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18943 | hp2 | a0001 | c0003 | t0003 | g0226 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18952 | hp2 | a0002 | c0001 | t0001 | g0301 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18953 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18953 | hp2 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0292 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18957 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18959 | hp1 | a0001 | c0003 | t0003 | g0039 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18960 | hp1 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18960 | hp2 | a0002 | c0001 | t0001 | g0057 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18962 | hp1 | a0002 | c0001 | t0001 | g0276 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18965 | hp2 | a0002 | c0001 | t0001 | g0272 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18966 | hp1 | a0001 | c0003 | t0003 | g0225 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0283 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18968 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18970 | hp2 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18971 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18977 | hp2 | a0001 | c0003 | t0003 | g0215 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18979 | hp1 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18981 | hp1 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18981 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18983 | hp1 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18983 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18985 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18986 | hp2 | a0009 | c0011 | t0001 | g0065 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18988 | hp1 | a0001 | c0003 | t0003 | g0233 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18989 | hp2 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18991 | hp2 | a0002 | c0001 | t0001 | g0061 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18992 | hp1 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18992 | hp2 | a0002 | c0001 | t0001 | g0274 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18994 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18995 | hp1 | a0001 | c0003 | t0005 | g0074 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18995 | hp2 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18998 | hp1 | a0008 | c0021 | t0001 | g0290 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18998 | hp2 | a0002 | c0001 | t0001 | g0060 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0038 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19002 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0288 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19006 | hp1 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0277 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19030 | hp1 | a0001 | c0017 | t0004 | g0220 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19030 | hp2 | a0005 | c0012 | t0001 | g0115 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19043 | hp2 | a0002 | c0001 | t0001 | g0112 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19054 | hp1 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19054 | hp2 | a0002 | c0001 | t0001 | g0056 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19056 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19056 | hp2 | a0004 | c0014 | t0001 | g0254 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19057 | hp2 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19058 | hp2 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19060 | hp1 | a0002 | c0001 | t0001 | g0260 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19062 | hp1 | a0001 | c0003 | t0003 | g0229 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19063 | hp1 | a0001 | c0003 | t0003 | g0211 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19064 | hp2 | a0001 | c0003 | t0003 | g0017 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19065 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19067 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19068 | hp2 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19070 | hp1 | a0001 | c0003 | t0003 | g0038 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0284 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19072 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19074 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19074 | hp2 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19075 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19078 | hp1 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19078 | hp2 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19079 | hp2 | a0001 | c0003 | t0003 | g0036 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19081 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19082 | hp1 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19082 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19083 | hp1 | a0001 | c0003 | t0003 | g0039 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19086 | hp1 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19086 | hp2 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19087 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19087 | hp2 | a0002 | c0001 | t0001 | g0059 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19090 | hp1 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0231 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA19240 | hp2 | a0002 | c0001 | t0001 | g0120 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20129 | hp1 | a0001 | c0008 | t0006 | g0088 | AFR | ASW | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ASW | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20752 | hp1 | a0001 | c0004 | t0001 | g0107 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0134 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20805 | hp1 | a0002 | c0001 | t0001 | g0270 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20805 | hp2 | a0001 | c0004 | t0001 | g0102 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02109 | hp1 | a0001 | c0003 | t0004 | g0052 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02109 | hp2 | a0001 | c0009 | t0004 | g0086 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02486 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02486 | hp2 | a0002 | c0001 | t0001 | g0098 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG02559 | hp2 | a0001 | c0007 | t0004 | g0136 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03471 | hp1 | a0001 | c0007 | t0004 | g0014 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG03471 | hp2 | a0001 | c0008 | t0006 | g0087 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG06807 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
HG06807 | hp2 | a0007 | c0015 | t0004 | g0304 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA21309 | hp1 | a0002 | c0001 | t0001 | g0123 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0221 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0067 | REF | REF | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0049 | REF | REF | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:43876681
|
C | A | 1 | a0006 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2782G>T | p.Val928Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2803/3571 | 2782/2796 | 928/931 | chr7 | 43876681 | ||
chr7:43876981
|
G | C | 1 | a0007 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2482C>G | p.Pro828Ala | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2503/3571 | 2482/2796 | 828/931 | chr7 | 43876981 | ||
chr7:43877037
|
G | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2426C>T | p.Thr809Met | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2447/3571 | 2426/2796 | 809/931 | chr7 | 43877037 | ||
chr7:43877128
|
T | G | 7 | a0002a0003a0004others(4): Show | 178 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
missense_variant | MODERATE | c.2335A>C | p.Met779Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2356/3571 | 2335/2796 | 779/931 | chr7 | 43877128 | ||
chr7:43877445
|
C | T | 1 | a0004 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.2018G>A | p.Arg673His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2039/3571 | 2018/2796 | 673/931 | chr7 | 43877445 | ||
chr7:43878795
|
T | G | 1 | a0008 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.668A>C | p.His223Pro | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 689/3571 | 668/2796 | 223/931 | chr7 | 43878795 | ||
chr7:43878964
|
C | T | 1 | a0009 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.499G>A | p.Asp167Asn | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 520/3571 | 499/2796 | 167/931 | chr7 | 43878964 | ||
chr7:43881662
|
T | C | 1 | a0003 | 3 | HG00438.hp2 HG03704.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.199A>G | p.Thr67Ala | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/6 | 220/3571 | 199/2796 | 67/931 | chr7 | 43881662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:43876682
|
C | A | 1 | a0006c0016 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.2781G>T | p.Leu927Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2802/3571 | 2781/2796 | 927/931 | chr7 | 43876682 | ||
chr7:43876727
|
G | A | 1 | a0001c0019 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2736C>T | p.Asn912Asn | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2757/3571 | 2736/2796 | 912/931 | chr7 | 43876727 | ||
chr7:43876814
|
G | A | 2 | a0001c0007a0001c0017 | 6 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
synonymous_variant | LOW | c.2649C>T | p.His883His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2670/3571 | 2649/2796 | 883/931 | chr7 | 43876814 | ||
chr7:43876892
|
G | A | 1 | a0001c0004 | 29 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(26): Show |
synonymous_variant | LOW | c.2571C>T | p.Asp857Asp | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2592/3571 | 2571/2796 | 857/931 | chr7 | 43876892 | ||
chr7:43877183
|
G | A | 1 | a0001c0007 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.2280C>T | p.Ala760Ala | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2301/3571 | 2280/2796 | 760/931 | chr7 | 43877183 | ||
chr7:43877414
|
G | A | 9 | a0002c0001a0002c0013a0002c0020others(6): Show | 170 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(167): Show |
synonymous_variant | LOW | c.2049C>T | p.His683His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2070/3571 | 2049/2796 | 683/931 | chr7 | 43877414 | ||
chr7:43877510
|
C | T | 1 | a0002c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.1953G>A | p.Ser651Ser | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1974/3571 | 1953/2796 | 651/931 | chr7 | 43877510 | ||
chr7:43877648
|
C | T | 1 | a0001c0008 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.1815G>A | p.Pro605Pro | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1836/3571 | 1815/2796 | 605/931 | chr7 | 43877648 | ||
chr7:43877657
|
C | A | 1 | a0001c0017 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1806G>T | p.Val602Val | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1827/3571 | 1806/2796 | 602/931 | chr7 | 43877657 | ||
chr7:43877660
|
G | A | 1 | a0001c0018 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1803C>T | p.Asp601Asp | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1824/3571 | 1803/2796 | 601/931 | chr7 | 43877660 | ||
chr7:43877675
|
A | G | 18 | a0001c0003a0001c0004a0001c0005others(15): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
synonymous_variant | LOW | c.1788T>C | p.His596His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1809/3571 | 1788/2796 | 596/931 | chr7 | 43877675 | ||
chr7:43877735
|
C | T | 1 | a0001c0007 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.1728G>A | p.Arg576Arg | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1749/3571 | 1728/2796 | 576/931 | chr7 | 43877735 | ||
chr7:43877866
|
G | A | 1 | a0001c0009 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.1597C>T | p.Leu533Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1618/3571 | 1597/2796 | 533/931 | chr7 | 43877866 | ||
chr7:43877987
|
G | A | 1 | a0002c0020 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1476C>T | p.Asp492Asp | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1497/3571 | 1476/2796 | 492/931 | chr7 | 43877987 | ||
chr7:43878005
|
C | T | 1 | a0001c0005 | 8 | HG01884.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.1458G>A | p.Ser486Ser | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1479/3571 | 1458/2796 | 486/931 | chr7 | 43878005 | ||
chr7:43878565
|
A | G | 1 | a0005c0012 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.898T>C | p.Leu300Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 919/3571 | 898/2796 | 300/931 | chr7 | 43878565 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:43876049
|
G | A | 1 | a0002c0001t0007 | 4 | HG00642.hp1 HG01106.hp1 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*618C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 618 | chr7 | 43876049 | |||||
chr7:43876104
|
G | A | 1 | a0001c0002t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 563 | chr7 | 43876104 | |||||
chr7:43876174
|
G | C | 1 | a0002c0001t0008 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 493 | chr7 | 43876174 | |||||
chr7:43876207
|
T | C | 5 | a0001c0003t0004a0001c0007t0004a0001c0009t0004others(2): Show | 16 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*460A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 460 | chr7 | 43876207 | |||||
chr7:43876306
|
C | A | 1 | a0002c0001t0009 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*361G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 361 | chr7 | 43876306 | |||||
chr7:43876410
|
G | A | 1 | a0001c0003t0005 | 11 | HG00323.hp2 HG00642.hp2 HG01069.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*257C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 257 | chr7 | 43876410 | |||||
chr7:43876529
|
C | CCT | 27 | a0001c0002t0006a0001c0002t0010a0001c0003t0001others(24): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*136_*137dupAG | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 137 | chr7 | 43876529 | |||||
chr7:43876539
|
C | G | 24 | a0001c0003t0001a0001c0003t0003a0001c0003t0004others(21): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*128G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 128 | chr7 | 43876539 | |||||
chr7:43876600
|
C | T | 4 | a0001c0003t0003a0001c0003t0005a0001c0005t0003others(1): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*67G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 67 | chr7 | 43876600 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:43879314
|
C | A | 2 | a0002c0001t0001g0260a0002c0001t0001g0284 | 2 | NA19060.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.203-54G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879314 | ||||||
chr7:43879415
|
G | C | 1 | a0001c0003t0003g0230 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.203-155C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879415 | ||||||
chr7:43879487
|
T | C | 1 | a0002c0001t0001g0292 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.203-227A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879487 | ||||||
chr7:43879645
|
T | C | 1 | a0002c0001t0001g0118 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.203-385A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879645 | ||||||
chr7:43879667
|
C | T | 218 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0002t0010g0135others(215): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.203-407G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879667 | ||||||
chr7:43879687
|
C | T | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.203-427G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879687 | ||||||
chr7:43879725
|
G | C | 3 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0002t0010g0135 | 3 | HG02055.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.203-465C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879725 | ||||||
chr7:43879752
|
T | C | 1 | a0001c0002t0010g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-492A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879752 | ||||||
chr7:43879774
|
G | GT | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.203-515dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879774 | ||||||
chr7:43880274
|
A | C | 1 | a0001c0017t0004g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.203-1014T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880274 | ||||||
chr7:43880577
|
G | C | 1 | a0001c0003t0003g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+1082C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880577 | ||||||
chr7:43880580
|
T | A | 1 | a0002c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.202+1079A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880580 | ||||||
chr7:43880587
|
G | A | 4 | a0002c0006t0001g0026a0002c0006t0001g0108a0002c0006t0001g0109others(1): Show | 5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+1072C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880587 | ||||||
chr7:43880636
|
G | T | 1 | a0002c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.202+1023C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880636 | ||||||
chr7:43880637
|
C | G | 1 | a0002c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.202+1022G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880637 | ||||||
chr7:43880755
|
A | G | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+904T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880755 | ||||||
chr7:43880826
|
A | G | 219 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0002t0010g0135others(216): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.202+833T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880826 | ||||||
chr7:43880931
|
C | T | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+728G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880931 | ||||||
chr7:43881017
|
G | C | 1 | a0003c0010t0001g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.202+642C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881017 | ||||||
chr7:43881102
|
G | A | 1 | a0002c0001t0001g0259 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.202+557C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881102 | ||||||
chr7:43881128
|
T | C | 1 | a0002c0001t0001g0238 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.202+531A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881128 | ||||||
chr7:43881217
|
T | C | 14 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0003t0004g0019others(11): Show | 18 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.202+442A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881217 | ||||||
chr7:43881318
|
G | A | 2 | a0002c0001t0007g0041a0002c0001t0007g0244 | 3 | HG00642.hp1 HG01109.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.202+341C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881318 | ||||||
chr7:43881474
|
G | GT | 40 | a0001c0002t0002g0139a0001c0002t0002g0151a0001c0002t0002g0167others(37): Show | 47 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.202+184dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881474 | ||||||
chr7:43881474
|
GT | G | 10 | a0001c0002t0002g0050a0001c0002t0002g0189a0001c0002t0002g0193others(7): Show | 14 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+184delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881474 | ||||||
chr7:43881481
|
T | TG | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.202+177_202+178ins others(1): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881481 | ||||||
chr7:43881642
|
G | A | 1 | a0001c0008t0006g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.202+17C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881642 | ||||||
chr7:43881761
|
T | G | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-64A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 4/5 | chr7 | 43881761 | ||||||
chr7:43881878
|
A | G | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.163+29T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 4/5 | chr7 | 43881878 | ||||||
chr7:43882012
|
T | C | 1 | a0002c0001t0009g0278 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.113-55A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882012 | ||||||
chr7:43882065
|
G | A | 2 | a0001c0002t0002g0165a0001c0002t0002g0198 | 2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.113-108C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882065 | ||||||
chr7:43882077
|
T | C | 1 | a0002c0001t0001g0279 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.113-120A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882077 | ||||||
chr7:43882089
|
G | T | 1 | a0001c0002t0002g0172 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.113-132C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882089 | ||||||
chr7:43882107
|
G | A | 1 | a0001c0002t0002g0201 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.113-150C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882107 | ||||||
chr7:43882133
|
A | T | 1 | a0002c0001t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.113-176T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882133 | ||||||
chr7:43882386
|
G | A | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.113-429C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882386 | ||||||
chr7:43882428
|
C | T | 1 | a0001c0017t0004g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113-471G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882428 | ||||||
chr7:43882463
|
A | C | 6 | a0001c0004t0001g0018a0001c0004t0001g0044a0001c0004t0001g0045others(3): Show | 7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-506T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882463 | ||||||
chr7:43882581
|
G | A | 1 | a0002c0001t0001g0062 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.113-624C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882581 | ||||||
chr7:43882607
|
C | CA | 32 | a0001c0002t0002g0203a0001c0002t0002g0205a0001c0003t0005g0079others(29): Show | 38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.113-651dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882607 | ||||||
chr7:43882747
|
T | C | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-790A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882747 | ||||||
chr7:43882887
|
C | A | 1 | a0002c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.113-930G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882887 | ||||||
chr7:43883014
|
G | A | 2 | a0001c0004t0001g0072a0001c0004t0001g0090 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.113-1057C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883014 | ||||||
chr7:43883321
|
A | AATATATA others(22): Show |
1 | a0001c0002t0002g0190 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-1365_113-1364i others(31): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | ||||||
chr7:43883321
|
AATATATA others(11): Show |
A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-1382_113-1365d others(20): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | ||||||
chr7:43883321
|
AATATATA others(13): Show |
A | 1 | a0001c0003t0004g0020 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.113-1384_113-1365d others(22): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | ||||||
chr7:43883321
|
AATATATA others(15): Show |
A | 4 | a0001c0003t0004g0019a0001c0003t0004g0052a0001c0003t0004g0305others(1): Show | 5 | HG02109.hp1 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1386_113-1365d others(24): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | ||||||
chr7:43883321
|
AATATATA others(17): Show |
A | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0017t0004g0220 | 5 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1388_113-1365d others(26): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | ||||||
chr7:43883335
|
T | C | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.113-1378A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883335 | ||||||
chr7:43883337
|
C | CAT | 18 | a0001c0002t0002g0035a0001c0002t0002g0150a0001c0002t0002g0172others(15): Show | 20 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.113-1382_113-1381d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | ||||||
chr7:43883337
|
C | CATAT | 3 | a0002c0001t0001g0292a0002c0001t0001g0301a0003c0010t0001g0256 | 3 | HG03704.hp1 NA18952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.113-1384_113-1381d others(6): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | ||||||
chr7:43883337
|
C | T | 1 | a0001c0007t0004g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113-1380G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | ||||||
chr7:43883337
|
CAT | C | 4 | a0001c0002t0006g0073a0001c0002t0006g0091a0002c0001t0001g0260others(1): Show | 4 | HG02965.hp1 HG03195.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1382_113-1381d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | ||||||
chr7:43883338
|
ATATATAT others(18): Show |
A | 1 | a0001c0007t0004g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113-1406_113-1382d others(27): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883338 | ||||||
chr7:43883339
|
T | TATATATA others(19): Show |
1 | a0001c0002t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.113-1383_113-1382i others(28): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883339 | ||||||
chr7:43883356
|
A | AT | 3 | a0001c0002t0002g0198a0002c0001t0001g0071a0002c0001t0001g0130 | 3 | HG01346.hp2 HG01928.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.113-1400dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883356 | ||||||
chr7:43883356
|
A | T | 1 | a0002c0001t0001g0021 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113-1399T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883356 | ||||||
chr7:43883358
|
A | AT | 7 | a0001c0002t0002g0015a0001c0002t0002g0146a0001c0002t0002g0165others(4): Show | 9 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-1402dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883358 | ||||||
chr7:43883358
|
A | ATTT | 6 | a0001c0004t0001g0018a0001c0004t0001g0044a0001c0004t0001g0045others(3): Show | 7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-1402_113-1401i others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883358 | ||||||
chr7:43883358
|
A | T | 15 | a0001c0002t0002g0198a0001c0004t0001g0090a0002c0001t0001g0021others(12): Show | 16 | HG00609.hp2 HG01243.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.113-1401T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883358 | ||||||
chr7:43883359
|
TA | T | 10 | a0001c0003t0003g0221a0001c0008t0006g0087a0002c0001t0001g0056others(7): Show | 11 | HG00438.hp1 HG02145.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.113-1403delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883359 | ||||||
chr7:43883360
|
A | AT | 13 | a0001c0003t0003g0229a0001c0005t0003g0007a0001c0005t0003g0219others(10): Show | 22 | HG00280.hp2 HG00738.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.113-1404dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883360 | ||||||
chr7:43883360
|
A | ATT | 4 | a0001c0003t0003g0227a0001c0003t0003g0232a0001c0018t0003g0218others(1): Show | 4 | HG02055.hp1 HG03540.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1404_113-1403i others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883360 | ||||||
chr7:43883360
|
A | T | 40 | a0001c0002t0002g0015a0001c0002t0002g0146a0001c0002t0002g0165others(37): Show | 45 | HG00609.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.113-1403T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883360 | ||||||
chr7:43883361
|
TA | T | 4 | a0001c0002t0002g0032a0001c0002t0002g0139a0001c0003t0003g0224others(1): Show | 5 | NA18939.hp1 NA18981.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-1405delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883361 | ||||||
chr7:43883362
|
A | AT | 20 | a0001c0002t0002g0163a0001c0005t0003g0213a0002c0001t0001g0006others(17): Show | 26 | HG00544.hp1 HG01255.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.113-1406dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | ||||||
chr7:43883362
|
A | ATAT | 7 | a0001c0002t0002g0148a0002c0001t0001g0043a0002c0001t0001g0063others(4): Show | 8 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-1406_113-1405i others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | ||||||
chr7:43883362
|
A | ATT | 7 | a0001c0003t0003g0038a0001c0005t0003g0222a0002c0001t0001g0029others(4): Show | 10 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-1407_113-1406d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | ||||||
chr7:43883362
|
A | ATTTTTT | 9 | a0001c0004t0001g0013a0001c0004t0001g0025a0001c0004t0001g0092others(6): Show | 12 | HG00140.hp1 HG00639.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-1411_113-1406d others(8): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | ||||||
chr7:43883362
|
A | T | 98 | a0001c0002t0002g0004a0001c0002t0002g0015a0001c0002t0002g0143others(95): Show | 130 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.113-1405T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | ||||||
chr7:43883362
|
AT | A | 6 | a0001c0002t0002g0164a0001c0002t0002g0180a0001c0008t0006g0089others(3): Show | 6 | HG01361.hp2 HG02071.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-1406delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | ||||||
chr7:43883363
|
T | TA | 4 | a0001c0002t0002g0175a0002c0001t0001g0210a0002c0001t0001g0272others(1): Show | 4 | HG02074.hp1 HG02074.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1407_113-1406i others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883363 | ||||||
chr7:43883363
|
T | TATA | 3 | a0001c0002t0002g0168a0002c0001t0001g0271a0002c0001t0001g0288 | 3 | NA18941.hp2 NA19005.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.113-1407_113-1406i others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883363 | ||||||
chr7:43883364
|
T | A | 62 | a0001c0002t0002g0085a0001c0002t0002g0145a0001c0002t0002g0149others(59): Show | 87 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.113-1407A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883364 | ||||||
chr7:43883365
|
T | A | 2 | a0002c0001t0001g0272a0002c0001t0001g0288 | 2 | NA18965.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.113-1408A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883365 | ||||||
chr7:43883366
|
T | A | 8 | a0001c0002t0002g0189a0001c0002t0002g0190a0001c0002t0002g0191others(5): Show | 8 | HG00323.hp1 HG00423.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-1409A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883366 | ||||||
chr7:43883368
|
T | A | 1 | a0002c0001t0001g0269 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.113-1411A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883368 | ||||||
chr7:43883413
|
C | T | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-1456G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883413 | ||||||
chr7:43883414
|
G | A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-1457C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883414 | ||||||
chr7:43883423
|
C | T | 2 | a0001c0004t0001g0072a0001c0004t0001g0090 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.113-1466G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883423 | ||||||
chr7:43883563
|
G | A | 135 | a0001c0003t0001g0291a0002c0001t0001g0001a0002c0001t0001g0006others(132): Show | 178 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.113-1606C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883563 | ||||||
chr7:43883605
|
C | T | 1 | a0001c0003t0003g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.113-1648G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883605 | ||||||
chr7:43883625
|
C | T | 1 | a0002c0001t0001g0251 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.113-1668G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883625 | ||||||
chr7:43883627
|
T | C | 219 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0002t0010g0135others(216): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.113-1670A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883627 | ||||||
chr7:43883691
|
T | G | 4 | a0002c0006t0001g0026a0002c0006t0001g0108a0002c0006t0001g0109others(1): Show | 5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1734A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883691 | ||||||
chr7:43883770
|
G | A | 2 | a0001c0004t0001g0100a0001c0004t0001g0105 | 2 | HG00140.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.113-1813C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883770 | ||||||
chr7:43883878
|
A | G | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.113-1921T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883878 | ||||||
chr7:43884084
|
A | T | 2 | a0002c0001t0001g0296a0002c0001t0001g0299 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.113-2127T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884084 | ||||||
chr7:43884085
|
C | T | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2128G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884085 | ||||||
chr7:43884132
|
G | C | 1 | a0002c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-2175C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884132 | ||||||
chr7:43884443
|
G | A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-2486C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884443 | ||||||
chr7:43884478
|
G | A | 1 | a0001c0002t0002g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.113-2521C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884478 | ||||||
chr7:43884552
|
G | T | 1 | a0001c0017t0004g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113-2595C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884552 | ||||||
chr7:43884558
|
G | A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-2601C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884558 | ||||||
chr7:43884691
|
G | T | 4 | a0002c0001t0001g0119a0002c0001t0001g0120a0002c0001t0001g0121others(1): Show | 4 | HG02809.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2724C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884691 | ||||||
chr7:43884699
|
T | C | 214 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0003t0001g0291others(211): Show | 281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.112+2716A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884699 | ||||||
chr7:43884716
|
C | A | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112+2699G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884716 | ||||||
chr7:43884802
|
T | G | 135 | a0001c0003t0001g0291a0002c0001t0001g0001a0002c0001t0001g0006others(132): Show | 178 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.112+2613A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884802 | ||||||
chr7:43885102
|
AT | A | 295 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(292): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.112+2312delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885102 | ||||||
chr7:43885102
|
ATT | A | 7 | a0001c0002t0002g0169a0001c0002t0002g0178a0001c0002t0010g0135others(4): Show | 7 | HG01256.hp2 HG01993.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+2311_112+2312d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885102 | ||||||
chr7:43885103
|
T | A | 1 | a0002c0001t0001g0272 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.112+2312A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885103 | ||||||
chr7:43885104
|
T | A | 209 | a0001c0003t0001g0291a0001c0003t0003g0005a0001c0003t0003g0017others(206): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.112+2311A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885104 | ||||||
chr7:43885105
|
T | A | 3 | a0001c0004t0001g0045a0001c0004t0001g0048a0002c0001t0001g0235 | 3 | HG01256.hp2 HG02735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.112+2310A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885105 | ||||||
chr7:43885139
|
C | T | 2 | a0001c0002t0002g0034a0001c0002t0002g0170 | 3 | NA18975.hp2 NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.112+2276G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885139 | ||||||
chr7:43885245
|
C | T | 2 | a0002c0001t0001g0054a0002c0001t0001g0055 | 2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.112+2170G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885245 | ||||||
chr7:43885289
|
C | T | 1 | a0001c0004t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.112+2126G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885289 | ||||||
chr7:43885387
|
C | T | 1 | a0001c0002t0002g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.112+2028G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885387 | ||||||
chr7:43885405
|
T | C | 1 | a0002c0001t0001g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.112+2010A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885405 | ||||||
chr7:43885445
|
T | G | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+1970A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885445 | ||||||
chr7:43885496
|
A | T | 1 | a0001c0004t0001g0090 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.112+1919T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885496 | ||||||
chr7:43885510
|
GAAC | G | 68 | a0001c0003t0001g0291a0002c0001t0001g0001a0002c0001t0001g0008others(65): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.112+1902_112+1904d others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885510 | ||||||
chr7:43885513
|
C | G | 151 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0002t0010g0135others(148): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.112+1902G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885513 | ||||||
chr7:43885554
|
G | A | 1 | a0001c0002t0002g0198 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.112+1861C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885554 | ||||||
chr7:43885665
|
A | C | 1 | a0002c0001t0001g0301 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.112+1750T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885665 | ||||||
chr7:43885714
|
G | A | 7 | a0001c0002t0002g0141a0001c0002t0002g0156a0001c0002t0002g0157others(4): Show | 7 | NA18939.hp2 NA18942.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+1701C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885714 | ||||||
chr7:43885749
|
A | G | 1 | a0002c0001t0001g0021 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.112+1666T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885749 | ||||||
chr7:43885758
|
C | A | 1 | a0002c0001t0001g0247 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.112+1657G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885758 | ||||||
chr7:43885901
|
G | A | 1 | a0001c0002t0002g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112+1514C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885901 | ||||||
chr7:43886225
|
C | T | 1 | a0001c0002t0010g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112+1190G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886225 | ||||||
chr7:43886263
|
C | T | 1 | a0001c0002t0002g0197 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.112+1152G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886263 | ||||||
chr7:43886374
|
ACT | A | 4 | a0001c0002t0002g0032a0001c0002t0002g0138a0001c0002t0002g0139others(1): Show | 5 | NA18939.hp1 NA18949.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+1039_112+1040d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886374 | ||||||
chr7:43886440
|
T | C | 17 | a0001c0004t0001g0013a0001c0004t0001g0025a0001c0004t0001g0092others(14): Show | 20 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.112+975A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886440 | ||||||
chr7:43886481
|
G | A | 1 | a0002c0001t0001g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.112+934C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886481 | ||||||
chr7:43886557
|
A | G | 1 | a0001c0017t0004g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112+858T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886557 | ||||||
chr7:43886709
|
C | T | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112+706G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886709 | ||||||
chr7:43886885
|
G | A | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+530C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886885 | ||||||
chr7:43886897
|
C | T | 2 | a0001c0002t0006g0073a0001c0002t0006g0091 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.112+518G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886897 | ||||||
chr7:43886898
|
C | T | 17 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0015others(14): Show | 33 | HG00423.hp1 HG00673.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.112+517G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886898 | ||||||
chr7:43886964
|
G | T | 1 | a0002c0001t0001g0250 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.112+451C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886964 | ||||||
chr7:43887040
|
T | C | 1 | a0001c0002t0002g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.112+375A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43887040 | ||||||
chr7:43887047
|
T | TA | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.112+367dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43887047 | ||||||
chr7:43887190
|
C | T | 12 | a0002c0001t0001g0113a0002c0001t0001g0114a0002c0001t0001g0116others(9): Show | 12 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.112+225G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43887190 | ||||||
chr7:43887536
|
T | A | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-51A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 2/5 | chr7 | 43887536 | ||||||
chr7:43888050
|
G | A | 2 | a0001c0004t0001g0072a0001c0004t0001g0090 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.15-234C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888050 | ||||||
chr7:43888074
|
A | C | 4 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0305others(1): Show | 6 | HG02258.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-258T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888074 | ||||||
chr7:43888081
|
G | A | 23 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(20): Show | 27 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.15-265C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888081 | ||||||
chr7:43888145
|
G | A | 1 | a0001c0002t0002g0141 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.15-329C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888145 | ||||||
chr7:43888154
|
G | C | 2 | a0001c0002t0006g0073a0001c0002t0006g0091 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.15-338C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888154 | ||||||
chr7:43888193
|
C | T | 214 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0003t0001g0291others(211): Show | 281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.15-377G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888193 | ||||||
chr7:43888363
|
G | A | 135 | a0001c0003t0001g0291a0002c0001t0001g0001a0002c0001t0001g0006others(132): Show | 178 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.15-547C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888363 | ||||||
chr7:43888473
|
C | T | 34 | a0002c0001t0001g0006a0002c0001t0001g0009a0002c0001t0001g0021others(31): Show | 44 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-657G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888473 | ||||||
chr7:43888501
|
C | CA | 18 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0004t0001g0013others(15): Show | 21 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-686dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888501 | ||||||
chr7:43888501
|
C | CAA | 7 | a0001c0004t0001g0093a0001c0007t0004g0014a0001c0007t0004g0136others(4): Show | 9 | HG00741.hp2 HG01517.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-687_15-686dupTT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888501 | ||||||
chr7:43888536
|
T | A | 1 | a0001c0002t0002g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15-720A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888536 | ||||||
chr7:43888564
|
T | C | 4 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137others(1): Show | 6 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-748A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888564 | ||||||
chr7:43888680
|
G | A | 304 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(301): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.15-864C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888680 | ||||||
chr7:43888750
|
A | G | 5 | a0001c0002t0006g0073a0001c0002t0006g0091a0001c0009t0004g0083others(2): Show | 5 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-934T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888750 | ||||||
chr7:43888885
|
C | T | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15-1069G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888885 | ||||||
chr7:43888886
|
G | A | 2 | a0002c0006t0001g0027a0002c0006t0001g0111 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.15-1070C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888886 | ||||||
chr7:43888974
|
C | T | 2 | a0002c0001t0001g0296a0002c0001t0001g0299 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.15-1158G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888974 | ||||||
chr7:43889072
|
C | G | 1 | a0002c0001t0001g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.15-1256G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889072 | ||||||
chr7:43889119
|
G | A | 1 | a0001c0002t0002g0200 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.15-1303C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889119 | ||||||
chr7:43889388
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.15-1572T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889388 | ||||||
chr7:43889391
|
C | T | 2 | a0001c0004t0001g0072a0001c0004t0001g0090 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.15-1575G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889391 | ||||||
chr7:43889493
|
G | A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-1677C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889493 | ||||||
chr7:43889599
|
A | T | 1 | a0002c0006t0001g0111 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15-1783T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889599 | ||||||
chr7:43889832
|
T | C | 11 | a0001c0002t0006g0073a0001c0003t0004g0019a0001c0003t0004g0020others(8): Show | 13 | HG00741.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-2016A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889832 | ||||||
chr7:43889907
|
A | AT | 33 | a0001c0002t0002g0156a0001c0002t0002g0159a0001c0002t0002g0164others(30): Show | 44 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.15-2092dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889907 | ||||||
chr7:43889907
|
AT | A | 8 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(5): Show | 10 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.15-2092delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889907 | ||||||
chr7:43889907
|
ATTT | A | 18 | a0001c0004t0001g0013a0001c0004t0001g0025a0001c0004t0001g0092others(15): Show | 21 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.15-2094_15-2092del others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889907 | ||||||
chr7:43890070
|
A | G | 1 | a0001c0002t0002g0162 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.15-2254T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890070 | ||||||
chr7:43890201
|
G | A | 2 | a0002c0001t0001g0042a0006c0016t0001g0273 | 3 | HG01261.hp1 HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.15-2385C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890201 | ||||||
chr7:43890213
|
C | CT | 65 | a0001c0002t0002g0139a0001c0002t0002g0142a0001c0002t0002g0145others(62): Show | 82 | HG00597.hp2 HG00642.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.15-2398dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890213 | ||||||
chr7:43890213
|
C | CTT | 27 | a0001c0003t0003g0037a0001c0003t0005g0074a0001c0004t0001g0013others(24): Show | 32 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.15-2399_15-2398dup others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890213 | ||||||
chr7:43890359
|
C | T | 3 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206 | 3 | HG02132.hp2 NA18954.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.15-2543G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890359 | ||||||
chr7:43890438
|
G | A | 1 | a0002c0001t0001g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.15-2622C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890438 | ||||||
chr7:43890491
|
C | A | 1 | a0002c0001t0001g0062 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.15-2675G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890491 | ||||||
chr7:43890505
|
C | T | 39 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(36): Show | 55 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.15-2689G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890505 | ||||||
chr7:43890775
|
G | C | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-2959C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890775 | ||||||
chr7:43890940
|
G | A | 1 | a0001c0008t0006g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-3124C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890940 | ||||||
chr7:43891005
|
G | T | 1 | a0002c0006t0001g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15-3189C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891005 | ||||||
chr7:43891006
|
C | G | 1 | a0001c0003t0005g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.15-3190G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891006 | ||||||
chr7:43891117
|
C | T | 5 | a0002c0001t0001g0118a0002c0001t0001g0119a0002c0001t0001g0120others(2): Show | 5 | HG01255.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-3301G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891117 | ||||||
chr7:43891172
|
T | C | 1 | a0001c0002t0010g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.15-3356A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891172 | ||||||
chr7:43891176
|
T | C | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.15-3360A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891176 | ||||||
chr7:43891321
|
ATACAGG | A | 3 | a0002c0001t0001g0063a0002c0001t0001g0064a0002c0001t0001g0066 | 3 | HG02523.hp2 NA18747.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.15-3511_15-3506del others(6): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891321 | ||||||
chr7:43891405
|
G | A | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.15-3589C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891405 | ||||||
chr7:43891439
|
AGCTGTAA others(4): Show |
A | 2 | a0001c0007t0004g0014a0001c0007t0004g0136 | 4 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-3634_15-3624del others(11): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891439 | ||||||
chr7:43891474
|
C | T | 1 | a0002c0001t0001g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15-3658G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891474 | ||||||
chr7:43891511
|
C | T | 1 | a0001c0004t0001g0100 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15-3695G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891511 | ||||||
chr7:43891691
|
C | T | 39 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(36): Show | 55 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.15-3875G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891691 | ||||||
chr7:43891838
|
A | C | 1 | a0001c0002t0002g0161 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.15-4022T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891838 | ||||||
chr7:43891868
|
C | T | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.15-4052G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891868 | ||||||
chr7:43891961
|
T | C | 1 | a0002c0001t0001g0058 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.15-4145A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891961 | ||||||
chr7:43892012
|
C | T | 1 | a0001c0003t0005g0160 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15-4196G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892012 | ||||||
chr7:43892169
|
T | C | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-4353A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892169 | ||||||
chr7:43892211
|
C | T | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.15-4395G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892211 | ||||||
chr7:43892219
|
A | AT | 70 | a0001c0002t0002g0051a0001c0002t0002g0085a0001c0002t0002g0139others(67): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.15-4404dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892219 | ||||||
chr7:43892219
|
A | ATT | 11 | a0001c0002t0010g0135a0001c0003t0003g0212a0001c0003t0003g0227others(8): Show | 11 | HG00597.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-4405_15-4404dup others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892219 | ||||||
chr7:43892219
|
AT | A | 5 | a0001c0002t0002g0181a0001c0002t0002g0182a0002c0001t0001g0028others(2): Show | 6 | HG03139.hp1 HG03490.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-4404delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892219 | ||||||
chr7:43892283
|
G | C | 1 | a0001c0003t0005g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.15-4467C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892283 | ||||||
chr7:43892738
|
A | G | 117 | a0001c0002t0002g0249a0001c0003t0001g0291a0001c0003t0004g0019others(114): Show | 152 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.15-4922T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892738 | ||||||
chr7:43892825
|
C | T | 1 | a0001c0003t0003g0217 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.15-5009G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892825 | ||||||
chr7:43893055
|
G | T | 1 | a0002c0001t0001g0241 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.15-5239C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893055 | ||||||
chr7:43893110
|
T | C | 6 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137others(3): Show | 8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-5294A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893110 | ||||||
chr7:43893311
|
T | G | 106 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(103): Show | 137 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.15-5495A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893311 | ||||||
chr7:43893340
|
T | C | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-5524A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893340 | ||||||
chr7:43893370
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15-5554T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893370 | ||||||
chr7:43893384
|
T | A | 1 | a0001c0002t0002g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15-5568A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893384 | ||||||
chr7:43893385
|
G | A | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-5569C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893385 | ||||||
chr7:43893427
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15-5611T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893427 | ||||||
chr7:43893562
|
T | C | 6 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137others(3): Show | 8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-5746A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893562 | ||||||
chr7:43893567
|
A | G | 80 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(77): Show | 107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.15-5751T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893567 | ||||||
chr7:43893574
|
G | A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-5758C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893574 | ||||||
chr7:43893696
|
C | A | 1 | a0001c0002t0002g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.15-5880G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893696 | ||||||
chr7:43893796
|
G | A | 1 | a0002c0001t0001g0275 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15-5980C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893796 | ||||||
chr7:43893802
|
C | T | 1 | a0007c0015t0004g0304 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.15-5986G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893802 | ||||||
chr7:43894063
|
A | G | 106 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(103): Show | 137 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.15-6247T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894063 | ||||||
chr7:43894085
|
T | G | 6 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137others(3): Show | 8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-6269A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894085 | ||||||
chr7:43894150
|
A | G | 6 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137others(3): Show | 8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-6334T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894150 | ||||||
chr7:43894224
|
T | C | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.15-6408A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894224 | ||||||
chr7:43894250
|
T | C | 1 | a0002c0001t0001g0276 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.15-6434A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894250 | ||||||
chr7:43894423
|
A | G | 2 | a0001c0004t0001g0044a0001c0004t0001g0045 | 2 | HG00735.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.15-6607T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894423 | ||||||
chr7:43894531
|
T | A | 1 | a0002c0001t0001g0277 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.15-6715A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894531 | ||||||
chr7:43894678
|
C | CAAAATCA others(33): Show |
1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15-6863_15-6862ins others(40): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894678 | ||||||
chr7:43895150
|
C | T | 1 | a0001c0004t0001g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15-7334G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895150 | ||||||
chr7:43895204
|
T | C | 3 | a0001c0002t0002g0141a0001c0002t0002g0157a0001c0002t0002g0183 | 3 | NA18939.hp2 NA18949.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.15-7388A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895204 | ||||||
chr7:43895218
|
T | A | 1 | a0001c0002t0002g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15-7402A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895218 | ||||||
chr7:43895256
|
G | C | 1 | a0002c0006t0001g0109 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.15-7440C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895256 | ||||||
chr7:43895286
|
G | C | 1 | a0002c0001t0009g0278 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.15-7470C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895286 | ||||||
chr7:43895345
|
TAAAA | T | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.15-7533_15-7530del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895345 | ||||||
chr7:43895375
|
G | T | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-7559C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895375 | ||||||
chr7:43895377
|
C | T | 2 | a0001c0004t0001g0096a0001c0004t0001g0097 | 2 | HG02602.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.15-7561G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895377 | ||||||
chr7:43895417
|
T | A | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15-7601A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895417 | ||||||
chr7:43895418
|
A | G | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-7602T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895418 | ||||||
chr7:43895597
|
C | T | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-7781G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895597 | ||||||
chr7:43895636
|
C | A | 105 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(102): Show | 136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.15-7820G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895636 | ||||||
chr7:43895640
|
G | A | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-7824C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895640 | ||||||
chr7:43895702
|
T | C | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-7886A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895702 | ||||||
chr7:43895712
|
G | A | 1 | a0002c0001t0001g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15-7896C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895712 | ||||||
chr7:43895747
|
G | T | 1 | a0001c0002t0002g0139 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.15-7931C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895747 | ||||||
chr7:43896158
|
T | C | 1 | a0002c0001t0001g0279 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.15-8342A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896158 | ||||||
chr7:43896190
|
T | C | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-8374A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896190 | ||||||
chr7:43896250
|
G | A | 3 | a0001c0009t0004g0083a0001c0009t0004g0084a0001c0009t0004g0086 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-8434C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896250 | ||||||
chr7:43896329
|
G | A | 3 | a0001c0002t0006g0091a0001c0002t0010g0135a0001c0004t0001g0090 | 3 | HG02055.hp2 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15-8513C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896329 | ||||||
chr7:43896452
|
C | A | 105 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(102): Show | 136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.15-8636G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896452 | ||||||
chr7:43896454
|
C | CA | 72 | a0001c0002t0002g0051a0001c0002t0002g0184a0001c0002t0002g0188others(69): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.15-8639dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896454 | ||||||
chr7:43896454
|
CA | C | 10 | a0001c0002t0002g0144a0001c0002t0002g0156a0001c0002t0002g0157others(7): Show | 12 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-8639delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896454 | ||||||
chr7:43896538
|
G | A | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.15-8722C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896538 | ||||||
chr7:43896617
|
C | T | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.15-8801G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896617 | ||||||
chr7:43896713
|
G | A | 7 | a0001c0002t0002g0185a0001c0002t0002g0186a0001c0002t0002g0187others(4): Show | 7 | HG00408.hp2 NA18747.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-8897C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896713 | ||||||
chr7:43896743
|
A | G | 4 | a0001c0002t0002g0085a0001c0009t0004g0083a0001c0009t0004g0084others(1): Show | 4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-8927T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896743 | ||||||
chr7:43896762
|
G | C | 6 | a0001c0002t0002g0016a0001c0002t0002g0189a0001c0002t0002g0190others(3): Show | 8 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-8946C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896762 | ||||||
chr7:43896873
|
C | T | 2 | a0002c0001t0001g0054a0002c0001t0001g0055 | 2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.15-9057G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896873 | ||||||
chr7:43897203
|
A | AAAAT | 4 | a0001c0002t0002g0085a0001c0009t0004g0083a0001c0009t0004g0084others(1): Show | 4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+9355_14+9358dup others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897203 | ||||||
chr7:43897203
|
A | AAAATAAA others(1): Show |
24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+9351_14+9358dup others(8): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897203 | ||||||
chr7:43897242
|
C | T | 4 | a0001c0002t0002g0085a0001c0009t0004g0083a0001c0009t0004g0084others(1): Show | 4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+9320G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897242 | ||||||
chr7:43897479
|
G | C | 1 | a0002c0001t0001g0284 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.14+9083C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897479 | ||||||
chr7:43897566
|
T | TG | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+8995dupC | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897566 | ||||||
chr7:43897613
|
T | A | 2 | a0002c0001t0001g0285a0002c0001t0001g0286 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.14+8949A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897613 | ||||||
chr7:43897738
|
C | T | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+8824G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897738 | ||||||
chr7:43897764
|
G | A | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+8798C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897764 | ||||||
chr7:43897991
|
G | A | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+8571C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897991 | ||||||
chr7:43898209
|
A | G | 1 | a0002c0001t0001g0240 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.14+8353T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898209 | ||||||
chr7:43898262
|
T | C | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+8300A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898262 | ||||||
chr7:43898268
|
A | C | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.14+8294T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898268 | ||||||
chr7:43898378
|
C | G | 1 | a0002c0001t0001g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.14+8184G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898378 | ||||||
chr7:43898384
|
G | C | 1 | a0001c0002t0002g0193 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.14+8178C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898384 | ||||||
chr7:43898481
|
A | G | 9 | a0001c0002t0002g0150a0001c0002t0002g0151a0001c0002t0002g0152others(6): Show | 9 | HG02280.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+8081T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898481 | ||||||
chr7:43898631
|
G | C | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+7931C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898631 | ||||||
chr7:43898746
|
A | AAAAT | 26 | a0001c0002t0002g0010a0001c0002t0002g0033a0001c0002t0002g0142others(23): Show | 36 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+7812_14+7815dup others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | ||||||
chr7:43898746
|
AAAAT | A | 18 | a0001c0002t0002g0194a0001c0002t0002g0195a0001c0002t0002g0196others(15): Show | 20 | HG00642.hp2 HG01167.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.14+7812_14+7815del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | ||||||
chr7:43898746
|
AAAATAAA others(1): Show |
A | 33 | a0001c0002t0002g0198a0001c0003t0003g0005a0001c0003t0003g0017others(30): Show | 49 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.14+7808_14+7815del others(8): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | ||||||
chr7:43898746
|
AAAATAAA others(5): Show |
A | 21 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(18): Show | 25 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.14+7804_14+7815del others(12): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | ||||||
chr7:43898746
|
AAAATAAA others(13): Show |
A | 2 | a0001c0004t0001g0106a0001c0004t0001g0107 | 2 | HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.14+7796_14+7815del others(20): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | ||||||
chr7:43898768
|
AATAAATA others(17): Show |
A | 1 | a0002c0001t0001g0292 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.14+7770_14+7793del others(24): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898768 | ||||||
chr7:43898772
|
AATAAATA others(13): Show |
A | 1 | a0002c0001t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.14+7770_14+7789del others(20): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898772 | ||||||
chr7:43898773
|
A | T | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+7789T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898773 | ||||||
chr7:43898776
|
AATAAATA others(9): Show |
A | 68 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(65): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.14+7770_14+7785del others(16): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898776 | ||||||
chr7:43898780
|
AATAAATA others(5): Show |
A | 5 | a0002c0001t0001g0295a0002c0001t0001g0296a0002c0001t0001g0297others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+7770_14+7781del others(12): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898780 | ||||||
chr7:43898788
|
AATTT | A | 10 | a0002c0001t0001g0030a0002c0001t0001g0043a0002c0001t0001g0114others(7): Show | 12 | HG00609.hp2 HG01884.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.14+7770_14+7773del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898788 | ||||||
chr7:43898791
|
T | A | 20 | a0002c0001t0001g0028a0002c0001t0001g0029a0002c0001t0001g0031others(17): Show | 23 | HG00738.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+7771A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898791 | ||||||
chr7:43898792
|
T | A | 20 | a0002c0001t0001g0028a0002c0001t0001g0029a0002c0001t0001g0031others(17): Show | 23 | HG00738.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+7770A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898792 | ||||||
chr7:43898819
|
T | A | 116 | a0001c0002t0002g0249a0001c0003t0001g0291a0001c0003t0004g0019others(113): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.14+7743A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898819 | ||||||
chr7:43898842
|
T | TAA | 9 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(6): Show | 12 | HG01109.hp1 HG01433.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.14+7718_14+7719dup others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898842 | ||||||
chr7:43898842
|
T | TAAA | 20 | a0002c0001t0001g0006a0002c0001t0001g0009a0002c0001t0001g0022others(17): Show | 29 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.14+7717_14+7719dup others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898842 | ||||||
chr7:43898900
|
C | T | 1 | a0002c0001t0001g0235 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.14+7662G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898900 | ||||||
chr7:43898943
|
C | T | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.14+7619G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898943 | ||||||
chr7:43898979
|
C | T | 1 | a0002c0001t0001g0239 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.14+7583G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898979 | ||||||
chr7:43899158
|
TA | T | 33 | a0001c0002t0002g0085a0001c0002t0006g0073a0001c0003t0003g0053others(30): Show | 45 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.14+7403delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899158 | ||||||
chr7:43899168
|
T | A | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+7394A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899168 | ||||||
chr7:43899247
|
G | A | 4 | a0002c0006t0001g0026a0002c0006t0001g0108a0002c0006t0001g0109others(1): Show | 5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+7315C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899247 | ||||||
chr7:43899284
|
AT | A | 32 | a0001c0002t0002g0199a0001c0002t0002g0200a0001c0002t0002g0201others(29): Show | 36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+7277delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899284 | ||||||
chr7:43899402
|
A | C | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+7160T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899402 | ||||||
chr7:43899542
|
C | G | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.14+7020G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899542 | ||||||
chr7:43899569
|
T | C | 1 | a0002c0001t0001g0082 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.14+6993A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899569 | ||||||
chr7:43899643
|
A | T | 1 | a0002c0001t0001g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.14+6919T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899643 | ||||||
chr7:43899669
|
C | A | 116 | a0001c0002t0002g0249a0001c0003t0001g0291a0001c0003t0004g0019others(113): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.14+6893G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899669 | ||||||
chr7:43899807
|
T | C | 1 | a0002c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14+6755A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899807 | ||||||
chr7:43899836
|
C | T | 220 | a0001c0002t0002g0085a0001c0002t0002g0249a0001c0002t0006g0073others(217): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.14+6726G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899836 | ||||||
chr7:43899904
|
G | A | 220 | a0001c0002t0002g0085a0001c0002t0002g0249a0001c0002t0006g0073others(217): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.14+6658C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899904 | ||||||
chr7:43900012
|
G | A | 1 | a0008c0021t0001g0290 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.14+6550C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900012 | ||||||
chr7:43900093
|
C | A | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+6469G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900093 | ||||||
chr7:43900128
|
C | G | 220 | a0001c0002t0002g0085a0001c0002t0002g0249a0001c0002t0006g0073others(217): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.14+6434G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900128 | ||||||
chr7:43900216
|
AG | A | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+6345delC | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900216 | ||||||
chr7:43900356
|
G | A | 4 | a0001c0002t0002g0085a0001c0009t0004g0083a0001c0009t0004g0084others(1): Show | 4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+6206C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900356 | ||||||
chr7:43900392
|
T | C | 4 | a0001c0002t0006g0091a0001c0002t0010g0135a0001c0004t0001g0090others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+6170A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900392 | ||||||
chr7:43900399
|
G | A | 1 | a0002c0006t0001g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+6163C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900399 | ||||||
chr7:43900403
|
T | C | 220 | a0001c0002t0002g0085a0001c0002t0002g0249a0001c0002t0006g0073others(217): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.14+6159A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900403 | ||||||
chr7:43900463
|
C | A | 39 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(36): Show | 55 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.14+6099G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900463 | ||||||
chr7:43900466
|
AAAC | A | 9 | a0001c0003t0003g0017a0001c0003t0003g0037a0001c0003t0003g0038others(6): Show | 13 | HG02015.hp2 NA18943.hp2 NA18970.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+6093_14+6095del others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900466 | ||||||
chr7:43900467
|
AAC | A | 29 | a0001c0003t0003g0005a0001c0003t0003g0036a0001c0003t0003g0039others(26): Show | 41 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.14+6093_14+6094del others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900467 | ||||||
chr7:43900469
|
C | A | 1 | a0001c0003t0003g0233 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.14+6093G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900469 | ||||||
chr7:43900469
|
CA | C | 143 | a0001c0002t0002g0144a0001c0002t0002g0249a0001c0002t0006g0091others(140): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.14+6092delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900469 | ||||||
chr7:43900481
|
A | AAAAAAG | 7 | a0001c0002t0002g0085a0001c0007t0004g0014a0001c0007t0004g0136others(4): Show | 9 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+6075_14+6080dup others(6): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900481 | ||||||
chr7:43900481
|
A | AAG | 24 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(21): Show | 34 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.14+6080_14+6081ins others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900481 | ||||||
chr7:43900492
|
A | G | 1 | a0001c0003t0003g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+6070T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900492 | ||||||
chr7:43900643
|
G | A | 1 | a0002c0001t0001g0069 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.14+5919C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900643 | ||||||
chr7:43900726
|
C | G | 7 | a0001c0002t0002g0085a0001c0007t0004g0014a0001c0007t0004g0136others(4): Show | 9 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+5836G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900726 | ||||||
chr7:43900861
|
G | A | 40 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(37): Show | 56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.14+5701C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900861 | ||||||
chr7:43901080
|
A | G | 3 | a0001c0002t0002g0010a0001c0002t0002g0142a0001c0002t0002g0143 | 6 | HG00597.hp1 HG02132.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+5482T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901080 | ||||||
chr7:43901121
|
A | C | 2 | a0001c0004t0001g0025a0001c0004t0001g0094 | 3 | HG01257.hp2 HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.14+5441T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901121 | ||||||
chr7:43901193
|
T | C | 1 | a0001c0002t0006g0091 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.14+5369A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901193 | ||||||
chr7:43901233
|
G | A | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+5329C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901233 | ||||||
chr7:43901763
|
G | A | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+4799C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901763 | ||||||
chr7:43901887
|
T | C | 1 | a0002c0001t0001g0082 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.14+4675A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901887 | ||||||
chr7:43901920
|
G | C | 9 | a0001c0003t0003g0017a0001c0003t0003g0037a0001c0003t0003g0038others(6): Show | 13 | HG02015.hp2 NA18943.hp2 NA18970.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+4642C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901920 | ||||||
chr7:43902004
|
A | G | 24 | a0001c0004t0001g0013a0001c0004t0001g0018a0001c0004t0001g0025others(21): Show | 28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+4558T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902004 | ||||||
chr7:43902025
|
G | A | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.14+4537C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902025 | ||||||
chr7:43902120
|
G | A | 6 | a0001c0004t0001g0018a0001c0004t0001g0044a0001c0004t0001g0045others(3): Show | 7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+4442C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902120 | ||||||
chr7:43902210
|
C | T | 68 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(65): Show | 94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.14+4352G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902210 | ||||||
chr7:43902327
|
ATCAC | A | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+4231_14+4234del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902327 | ||||||
chr7:43902565
|
G | A | 1 | a0002c0006t0001g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+3997C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902565 | ||||||
chr7:43902581
|
G | A | 1 | a0002c0001t0001g0301 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.14+3981C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902581 | ||||||
chr7:43902640
|
T | C | 2 | a0002c0001t0001g0070a0002c0001t0001g0071 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.14+3922A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902640 | ||||||
chr7:43902641
|
A | C | 2 | a0001c0004t0001g0092a0001c0004t0001g0093 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.14+3921T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902641 | ||||||
chr7:43902706
|
C | T | 79 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(76): Show | 106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.14+3856G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902706 | ||||||
chr7:43902731
|
G | A | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+3831C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902731 | ||||||
chr7:43903007
|
G | A | 1 | a0001c0002t0002g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.14+3555C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903007 | ||||||
chr7:43903115
|
C | T | 172 | a0001c0002t0002g0085a0001c0002t0002g0249a0001c0002t0006g0073others(169): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.14+3447G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903115 | ||||||
chr7:43903122
|
T | TA | 30 | a0001c0002t0002g0203a0001c0004t0001g0013a0001c0004t0001g0018others(27): Show | 34 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.14+3439dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903122 | ||||||
chr7:43903122
|
TA | T | 8 | a0001c0002t0002g0032a0001c0002t0002g0139a0001c0002t0002g0140others(5): Show | 9 | HG01168.hp2 HG01516.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+3439delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903122 | ||||||
chr7:43903135
|
A | G | 71 | a0001c0002t0006g0073a0001c0003t0003g0005a0001c0003t0003g0017others(68): Show | 98 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.14+3427T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903135 | ||||||
chr7:43903136
|
AGAGAG | A | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+3421_14+3425del others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903136 | ||||||
chr7:43903149
|
A | G | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+3413T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903149 | ||||||
chr7:43903177
|
A | G | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.14+3385T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903177 | ||||||
chr7:43903205
|
G | A | 1 | a0002c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.14+3357C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903205 | ||||||
chr7:43903326
|
T | C | 3 | a0001c0003t0003g0039a0001c0003t0003g0232a0001c0003t0003g0233 | 4 | NA18959.hp1 NA18988.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+3236A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903326 | ||||||
chr7:43903390
|
C | T | 115 | a0001c0002t0002g0249a0001c0003t0001g0291a0001c0003t0004g0019others(112): Show | 150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.14+3172G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903390 | ||||||
chr7:43903469
|
T | C | 1 | a0002c0001t0001g0134 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.14+3093A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903469 | ||||||
chr7:43903663
|
C | G | 1 | a0002c0001t0001g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.14+2899G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903663 | ||||||
chr7:43903746
|
C | G | 1 | a0002c0001t0001g0113 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.14+2816G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903746 | ||||||
chr7:43903750
|
GGGAC | G | 3 | a0001c0008t0006g0087a0001c0008t0006g0088a0001c0008t0006g0089 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.14+2808_14+2811del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903750 | ||||||
chr7:43903769
|
C | G | 1 | a0002c0001t0001g0236 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.14+2793G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903769 | ||||||
chr7:43903896
|
C | T | 1 | a0001c0009t0004g0083 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+2666G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903896 | ||||||
chr7:43903944
|
T | G | 1 | a0002c0001t0001g0302 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14+2618A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903944 | ||||||
chr7:43903970
|
G | C | 115 | a0001c0002t0002g0249a0001c0003t0001g0291a0001c0003t0004g0019others(112): Show | 150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.14+2592C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903970 | ||||||
chr7:43904010
|
C | T | 1 | a0001c0009t0004g0083 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+2552G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904010 | ||||||
chr7:43904118
|
T | G | 33 | a0001c0002t0002g0085a0001c0002t0006g0073a0001c0003t0003g0053others(30): Show | 45 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.14+2444A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904118 | ||||||
chr7:43904265
|
T | G | 2 | a0001c0002t0006g0073a0001c0004t0001g0072 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.14+2297A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904265 | ||||||
chr7:43904278
|
A | T | 33 | a0001c0002t0002g0085a0001c0002t0006g0073a0001c0003t0003g0053others(30): Show | 45 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.14+2284T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904278 | ||||||
chr7:43904486
|
A | C | 1 | a0001c0002t0010g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.14+2076T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904486 | ||||||
chr7:43904544
|
G | A | 3 | a0001c0002t0002g0204a0001c0002t0002g0205a0001c0002t0002g0206 | 3 | HG02132.hp2 NA18954.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.14+2018C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904544 | ||||||
chr7:43904703
|
G | T | 1 | a0002c0001t0001g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14+1859C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904703 | ||||||
chr7:43904758
|
G | A | 1 | a0001c0003t0004g0020 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.14+1804C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904758 | ||||||
chr7:43904968
|
A | G | 41 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(38): Show | 57 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.14+1594T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904968 | ||||||
chr7:43905088
|
A | T | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+1474T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905088 | ||||||
chr7:43905224
|
G | C | 3 | a0001c0002t0002g0207a0001c0002t0002g0208a0001c0002t0002g0209 | 3 | HG01255.hp2 HG01516.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.14+1338C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905224 | ||||||
chr7:43905242
|
T | G | 105 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(102): Show | 136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.14+1320A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905242 | ||||||
chr7:43905272
|
C | CT | 26 | a0001c0002t0006g0073a0001c0003t0003g0053a0001c0004t0001g0072others(23): Show | 36 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+1289dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905272 | ||||||
chr7:43905276
|
G | GC | 304 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(301): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.14+1285dupG | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905276 | ||||||
chr7:43905331
|
G | A | 1 | a0001c0002t0010g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.14+1231C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905331 | ||||||
chr7:43905547
|
T | C | 1 | a0001c0002t0010g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.14+1015A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905547 | ||||||
chr7:43905596
|
C | A | 3 | a0001c0007t0004g0014a0001c0007t0004g0136a0001c0007t0004g0137 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+966G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905596 | ||||||
chr7:43905597
|
C | G | 5 | a0001c0003t0004g0019a0001c0003t0004g0020a0001c0003t0004g0052others(2): Show | 7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+965G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905597 | ||||||
chr7:43905603
|
C | T | 1 | a0001c0002t0002g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.14+959G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905603 | ||||||
chr7:43905627
|
A | C | 1 | a0002c0001t0001g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.14+935T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905627 | ||||||
chr7:43905728
|
T | C | 1 | a0002c0001t0001g0303 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.14+834A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905728 | ||||||
chr7:43905897
|
G | A | 31 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(28): Show | 46 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(43): Show |
intron_variant | MODIFIER | c.14+665C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905897 | ||||||
chr7:43905898
|
C | A | 31 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(28): Show | 46 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(43): Show |
intron_variant | MODIFIER | c.14+664G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905898 | ||||||
chr7:43906162
|
C | T | 220 | a0001c0002t0002g0085a0001c0002t0002g0249a0001c0002t0006g0073others(217): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.14+400G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906162 | ||||||
chr7:43906195
|
G | A | 31 | a0001c0003t0003g0005a0001c0003t0003g0017a0001c0003t0003g0036others(28): Show | 46 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(43): Show |
intron_variant | MODIFIER | c.14+367C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906195 | ||||||
chr7:43906204
|
G | T | 2 | a0001c0002t0002g0050a0001c0002t0002g0051 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14+358C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906204 | ||||||
chr7:43906290
|
G | A | 78 | a0001c0002t0002g0249a0001c0003t0001g0291a0002c0001t0001g0001others(75): Show | 105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.14+272C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906290 | ||||||
chr7:43906383
|
G | GC | 304 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(301): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.14+178_14+179insG | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906383 | ||||||
chr7:43906431
|
C | A | 2 | a0001c0003t0004g0305a0007c0015t0004g0304 | 2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.14+131G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906431 | ||||||
chr7:43906435
|
C | T | 6 | a0001c0004t0001g0018a0001c0004t0001g0044a0001c0004t0001g0045others(3): Show | 7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+127G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906435 |