geneid | 55825 |
---|---|
ensemblid | ENSG00000115425.14 |
hgncid | 18281 |
symbol | PECR |
name | peroxisomal trans-2-enoyl-CoA reductase |
refseq_nuc | NM_018441.6 |
refseq_prot | NP_060911.2 |
ensembl_nuc | ENST00000265322.8 |
ensembl_prot | ENSP00000265322.7 |
mane_status | MANE Select |
chr | chr2 |
start | 216038388 |
end | 216081809 |
strand | - |
ver | v1.2 |
region | chr2:216038388-216081809 |
region5000 | chr2:216033388-216086809 |
regionname0 | PECR_chr2_216038388_216081809 |
regionname5000 | PECR_chr2_216033388_216086809 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 303 | 297 | 71 | 64 | 121 | 15 | 24 | 83 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0002 | 0/0 | 303 | 86 | 20 | 10 | 43 | 0 | 13 | 37 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0003 | 0/0 | 303 | 3 | 0 | 1 | 1 | 0 | 1 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0004 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0005 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0006 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0007 | 0/0 | 303 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0008 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0009 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0010 | 0/0 | 303 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0011 | 0/0 | 11 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 912 | 254 | 64 | 54 | 105 | 12 | 17 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0002 | 0/0 | 912 | 86 | 20 | 10 | 43 | 0 | 13 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0003 | 0/0 | 912 | 39 | 3 | 10 | 16 | 3 | 7 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0004 | 0/0 | 912 | 3 | 3 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0005 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0006 | 0/0 | 912 | 2 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0007 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0008 | 0/0 | 912 | 2 | 1 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0009 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0010 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0012 | 0/0 | 912 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0013 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0014 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
c0015 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 956 | 231 | 44 | 49 | 106 | 11 | 19 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0002 | 0/0 | 956 | 88 | 21 | 9 | 44 | 0 | 14 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0003 | 0/0 | 956 | 38 | 3 | 10 | 14 | 4 | 7 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0004 | 0/0 | 956 | 19 | 15 | 3 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0005 | 0/0 | 956 | 10 | 10 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0006 | 0/0 | 956 | 3 | 3 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0007 | 0/0 | 956 | 3 | 0 | 3 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0008 | 0/0 | 956 | 3 | 0 | 1 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0009 | 0/0 | 956 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
t0010 | 0/0 | 956 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 912 | 254 | 64 | 54 | 105 | 12 | 17 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0003 | 0/0 | 912 | 39 | 3 | 10 | 16 | 3 | 7 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0004 | 0/0 | 912 | 3 | 3 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0011 | 0/0 | 912 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0002c0002 | 0/0 | 912 | 86 | 20 | 10 | 43 | 0 | 13 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0003c0006 | 0/0 | 912 | 2 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0003c0014 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0004c0009 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0005c0007 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0006c0005 | 0/0 | 912 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0007c0008 | 0/0 | 912 | 2 | 1 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0008c0015 | 0/0 | 912 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0009c0013 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0010c0012 | 0/0 | 912 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0011c0010 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1867 | 217 | 37 | 47 | 103 | 11 | 17 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0001t0004 | 0/0 | 1867 | 19 | 15 | 3 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0001t0005 | 0/0 | 1867 | 10 | 10 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0001t0006 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0001t0007 | 0/0 | 1867 | 3 | 0 | 3 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0001t0008 | 0/0 | 1867 | 3 | 0 | 1 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0003t0001 | 0/0 | 1867 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0003t0003 | 0/0 | 1867 | 37 | 3 | 10 | 14 | 3 | 7 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0004t0001 | 0/0 | 1867 | 3 | 3 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0001c0011t0006 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0002c0002t0002 | 0/0 | 1867 | 85 | 20 | 9 | 43 | 0 | 13 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0002c0002t0010 | 0/0 | 1867 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0003c0006t0001 | 0/0 | 1867 | 2 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0003c0014t0001 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0004c0009t0001 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0005c0007t0001 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0006c0005t0009 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0007c0008t0002 | 0/0 | 1867 | 2 | 1 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0008c0015t0001 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0009c0013t0002 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0010c0012t0003 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
a0011c0010t0001 | 0/0 | 1867 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | copy fasta | chr2 | 216033388 | 216086809 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0004g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0005g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0008g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0003t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0004t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0001c0011t0006g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0002c0002t0010g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0003c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0003c0006t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0003c0014t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0004c0009t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0005c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0005c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0006c0005t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0006c0005t0009g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0007c0008t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0007c0008t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0008c0015t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0009c0013t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0010c0012t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
a0011c0010t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00140 | hp2 | a0001 | c0003 | t0003 | g0094 | EUR | GBR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00733 | hp1 | a0001 | c0003 | t0003 | g0183 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00738 | hp2 | a0001 | c0003 | t0003 | g0015 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00741 | hp1 | a0001 | c0003 | t0003 | g0188 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01070 | hp2 | a0002 | c0002 | t0010 | g0336 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0072 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0074 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0382 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0327 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01167 | hp2 | a0001 | c0003 | t0003 | g0011 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01169 | hp2 | a0001 | c0003 | t0003 | g0011 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0331 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01243 | hp2 | a0001 | c0003 | t0003 | g0203 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01255 | hp1 | a0003 | c0006 | t0001 | g0233 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01256 | hp2 | a0001 | c0003 | t0003 | g0206 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01258 | hp2 | a0001 | c0003 | t0003 | g0205 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0374 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01358 | hp1 | a0001 | c0003 | t0003 | g0185 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0075 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01361 | hp1 | a0011 | c0010 | t0001 | g0013 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0373 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0266 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01515 | hp2 | a0001 | c0003 | t0003 | g0186 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01517 | hp1 | a0001 | c0003 | t0003 | g0187 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0378 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0365 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0319 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0337 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01943 | hp2 | a0001 | c0001 | t0007 | g0079 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0344 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02071 | hp1 | a0001 | c0003 | t0003 | g0195 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0192 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0090 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0351 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0317 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0334 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0386 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0278 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0315 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02572 | hp1 | a0007 | c0008 | t0002 | g0321 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0328 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0357 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0325 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0211 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0379 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0375 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0189 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0367 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02735 | hp1 | a0001 | c0003 | t0003 | g0207 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0372 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0368 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0353 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0324 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0352 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02895 | hp2 | a0004 | c0009 | t0001 | g0012 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0359 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0310 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0358 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02897 | hp2 | a0004 | c0009 | t0001 | g0012 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0318 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0335 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03017 | hp1 | a0007 | c0008 | t0002 | g0259 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0313 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0326 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0366 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03195 | hp1 | a0001 | c0003 | t0003 | g0100 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03195 | hp2 | a0005 | c0007 | t0001 | g0021 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0376 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03486 | hp2 | a0006 | c0005 | t0009 | g0217 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03492 | hp1 | a0001 | c0003 | t0003 | g0095 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0380 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03579 | hp1 | a0005 | c0007 | t0001 | g0022 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03579 | hp2 | a0001 | c0011 | t0006 | g0383 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0371 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03669 | hp1 | a0001 | c0003 | t0003 | g0204 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0073 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03710 | hp2 | a0001 | c0003 | t0003 | g0234 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0225 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03834 | hp1 | a0003 | c0006 | t0001 | g0223 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0236 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0240 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03942 | hp1 | a0001 | c0003 | t0003 | g0301 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03942 | hp2 | a0001 | c0003 | t0003 | g0093 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04184 | hp1 | a0001 | c0003 | t0003 | g0208 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0248 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0256 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0229 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0070 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0246 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18522 | hp1 | a0001 | c0003 | t0003 | g0098 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0370 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18952 | hp1 | a0001 | c0003 | t0003 | g0091 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18952 | hp2 | a0001 | c0003 | t0003 | g0190 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18964 | hp1 | a0001 | c0003 | t0003 | g0348 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18979 | hp1 | a0003 | c0014 | t0001 | g0250 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18984 | hp2 | a0001 | c0001 | t0008 | g0293 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18986 | hp1 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18990 | hp1 | a0001 | c0003 | t0003 | g0197 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18998 | hp1 | a0001 | c0003 | t0003 | g0193 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19004 | hp1 | a0001 | c0003 | t0003 | g0194 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0340 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0369 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0356 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19043 | hp2 | a0002 | c0002 | t0002 | g0362 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19058 | hp1 | a0001 | c0003 | t0003 | g0191 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19058 | hp2 | a0009 | c0013 | t0002 | g0245 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19063 | hp1 | a0001 | c0003 | t0003 | g0142 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0347 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0342 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0339 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19067 | hp2 | a0001 | c0001 | t0008 | g0277 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19083 | hp1 | a0001 | c0003 | t0003 | g0241 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19083 | hp2 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19085 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19089 | hp1 | a0001 | c0003 | t0003 | g0242 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0332 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0355 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | ASW | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ASW | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20752 | hp1 | a0010 | c0012 | t0003 | g0215 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20905 | hp2 | a0008 | c0015 | t0001 | g0258 | SAS | GIH | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0341 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02109 | hp1 | a0006 | c0005 | t0009 | g0381 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0354 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0314 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0385 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0345 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0268 | REF | REF | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:216039296
|
A | T | 3 | a0002a0007a0009 | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
missense_variant | MODERATE | c.891T>A | p.Phe297Leu | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 959/1867 | 891/912 | 297/303 | chr2 | 216039296 | ||
chr2:216043934
|
T | C | 2 | a0006a0010 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.796A>G | p.Ser266Gly | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/8 | 864/1867 | 796/912 | 266/303 | chr2 | 216043934 | ||
chr2:216051478
|
T | C | 1 | a0010 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.574A>G | p.Ser192Gly | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/8 | 642/1867 | 574/912 | 192/303 | chr2 | 216051478 | ||
chr2:216058896
|
C | G | 1 | a0005 | 2 | HG03195.hp2 HG03579.hp1 |
missense_variant&splice_region_variant | MODERATE | c.505G>C | p.Val169Leu | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/8 | 573/1867 | 505/912 | 169/303 | chr2 | 216058896 | ||
chr2:216058956
|
C | T | 3 | a0002a0003a0009 | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
missense_variant | MODERATE | c.445G>A | p.Glu149Lys | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/8 | 513/1867 | 445/912 | 149/303 | chr2 | 216058956 | ||
chr2:216065443
|
A | C | 1 | a0009 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.293T>G | p.Phe98Cys | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/8 | 361/1867 | 293/912 | 98/303 | chr2 | 216065443 | ||
chr2:216066410
|
T | G | 1 | a0008 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.233A>C | p.Gln78Pro | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/8 | 301/1867 | 233/912 | 78/303 | chr2 | 216066410 | ||
chr2:216081713
|
T | C | 1 | a0004 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.29A>G | p.Tyr10Cys | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/8 | 97/1867 | 29/912 | 10/303 | chr2 | 216081713 | ||
chr2:216081740
|
A | G | 1 | a0011 | 1 | HG01361.hp1 | start_lost | HIGH | c.2T>C | p.Met1? | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/8 | 70/1867 | 2/912 | 1/303 | chr2 | 216081740 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:216043956
|
C | T | 2 | a0001c0003a0003c0014 | 40 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.774G>A | p.Ser258Ser | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/8 | 842/1867 | 774/912 | 258/303 | chr2 | 216043956 | ||
chr2:216066394
|
A | G | 3 | a0001c0011a0006c0005a0010c0012 | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.249T>C | p.Asn83Asn | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/8 | 317/1867 | 249/912 | 83/303 | chr2 | 216066394 | ||
chr2:216066460
|
T | C | 1 | a0001c0004 | 3 | HG02145.hp2 HG02647.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.183A>G | p.Glu61Glu | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/8 | 251/1867 | 183/912 | 61/303 | chr2 | 216066460 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:216038534
|
A | C | 2 | a0001c0003t0003a0010c0012t0003 | 38 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*741T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 741 | chr2 | 216038534 | |||||
chr2:216038554
|
C | T | 2 | a0001c0001t0006a0001c0011t0006 | 3 | HG02145.hp1 HG03579.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*721G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 721 | chr2 | 216038554 | |||||
chr2:216038555
|
G | A | 1 | a0001c0001t0005 | 10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 720 | chr2 | 216038555 | |||||
chr2:216038567
|
G | A | 10 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(7): Show | 159 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*708C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 708 | chr2 | 216038567 | |||||
chr2:216038584
|
A | T | 1 | a0001c0001t0008 | 3 | HG02293.hp2 NA18984.hp2 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*691T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 691 | chr2 | 216038584 | |||||
chr2:216038632
|
A | T | 1 | a0001c0001t0007 | 3 | HG01106.hp2 HG01358.hp2 HG01943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 643 | chr2 | 216038632 | |||||
chr2:216038771
|
C | T | 2 | a0001c0001t0006a0001c0011t0006 | 3 | HG02145.hp1 HG03579.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*504G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 504 | chr2 | 216038771 | |||||
chr2:216039163
|
T | C | 1 | a0002c0002t0010 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 112 | chr2 | 216039163 | |||||
chr2:216039171
|
A | C | 4 | a0002c0002t0002a0002c0002t0010a0007c0008t0002others(1): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 104 | chr2 | 216039171 | |||||
chr2:216039247
|
G | A | 1 | a0006c0005t0009 | 2 | HG02109.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*28C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 28 | chr2 | 216039247 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:216039676
|
C | T | 55 | a0002c0002t0002g0060a0002c0002t0002g0070a0002c0002t0002g0073others(52): Show | 55 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.827-316G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039676 | ||||||
chr2:216039803
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.827-443A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039803 | ||||||
chr2:216039874
|
T | G | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-514A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039874 | ||||||
chr2:216039997
|
GCAT | G | 3 | a0001c0001t0006g0023a0001c0001t0006g0099a0001c0011t0006g0383 | 3 | HG02145.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.827-640_827-638del others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039997 | ||||||
chr2:216040116
|
CAG | C | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-758_827-757del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040116 | ||||||
chr2:216040137
|
A | T | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-777T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040137 | ||||||
chr2:216040153
|
A | G | 10 | a0002c0002t0002g0326a0002c0002t0002g0327a0002c0002t0002g0328others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.827-793T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040153 | ||||||
chr2:216040211
|
G | C | 6 | a0002c0002t0002g0366a0002c0002t0002g0367a0002c0002t0002g0368others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-851C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040211 | ||||||
chr2:216040286
|
A | G | 36 | a0001c0003t0003g0011a0001c0003t0003g0015a0001c0003t0003g0072others(33): Show | 37 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.827-926T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040286 | ||||||
chr2:216040293
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.827-933A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040293 | ||||||
chr2:216040294
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.827-934C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040294 | ||||||
chr2:216040314
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.827-954C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040314 | ||||||
chr2:216040316
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.827-956C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040316 | ||||||
chr2:216040348
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0218 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.827-988C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040348 | ||||||
chr2:216040403
|
C | A | 42 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(39): Show | 43 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.827-1043G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040403 | ||||||
chr2:216040477
|
T | C | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1117A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040477 | ||||||
chr2:216040511
|
C | T | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1151G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040511 | ||||||
chr2:216040513
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.827-1153G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040513 | ||||||
chr2:216040547
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.827-1187G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040547 | ||||||
chr2:216040598
|
G | A | 1 | a0002c0002t0002g0240 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.827-1238C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040598 | ||||||
chr2:216040634
|
C | T | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1274G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040634 | ||||||
chr2:216040672
|
T | C | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1312A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040672 | ||||||
chr2:216040957
|
C | T | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1597G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040957 | ||||||
chr2:216040978
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.827-1618A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040978 | ||||||
chr2:216041005
|
G | A | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1645C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041005 | ||||||
chr2:216041049
|
C | T | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1689G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041049 | ||||||
chr2:216041083
|
G | A | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1723C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041083 | ||||||
chr2:216041144
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.827-1784G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041144 | ||||||
chr2:216041145
|
G | A | 1 | a0002c0002t0002g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.827-1785C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041145 | ||||||
chr2:216041203
|
AG | A | 6 | a0002c0002t0002g0366a0002c0002t0002g0367a0002c0002t0002g0368others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-1844delC | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041203 | ||||||
chr2:216041204
|
G | A | 82 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(79): Show | 83 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.827-1844C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041204 | ||||||
chr2:216041299
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.827-1939G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041299 | ||||||
chr2:216041307
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.827-1947A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041307 | ||||||
chr2:216041508
|
C | CTA | 50 | a0002c0002t0002g0060a0002c0002t0002g0070a0002c0002t0002g0073others(47): Show | 50 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.827-2150_827-2149d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041508 | ||||||
chr2:216041547
|
C | T | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-2187G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041547 | ||||||
chr2:216041570
|
T | C | 25 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0092others(22): Show | 26 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.827-2210A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041570 | ||||||
chr2:216041604
|
A | G | 6 | a0001c0001t0001g0105a0001c0001t0001g0147a0001c0001t0001g0163others(3): Show | 6 | HG00438.hp2 HG00673.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-2244T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041604 | ||||||
chr2:216041671
|
C | T | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+2233G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041671 | ||||||
chr2:216041714
|
C | G | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+2190G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041714 | ||||||
chr2:216041879
|
G | C | 1 | a0001c0001t0004g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826+2025C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041879 | ||||||
chr2:216041941
|
C | T | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+1963G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041941 | ||||||
chr2:216042157
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.826+1747C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042157 | ||||||
chr2:216042369
|
C | T | 24 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0092others(21): Show | 25 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.826+1535G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042369 | ||||||
chr2:216042374
|
A | C | 6 | a0002c0002t0002g0366a0002c0002t0002g0367a0002c0002t0002g0368others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+1530T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042374 | ||||||
chr2:216042475
|
C | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.826+1429G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042475 | ||||||
chr2:216042495
|
A | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+1409T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042495 | ||||||
chr2:216042535
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.826+1369A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042535 | ||||||
chr2:216042543
|
C | T | 3 | a0001c0003t0003g0190a0001c0003t0003g0192a0001c0003t0003g0193 | 3 | HG02132.hp1 NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.826+1361G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042543 | ||||||
chr2:216042580
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.826+1324G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042580 | ||||||
chr2:216042599
|
G | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.826+1305C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042599 | ||||||
chr2:216042637
|
C | T | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+1267G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042637 | ||||||
chr2:216042704
|
C | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0297others(1): Show | 4 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+1200G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042704 | ||||||
chr2:216042789
|
G | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(270): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.826+1115C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042789 | ||||||
chr2:216042906
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.826+998C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042906 | ||||||
chr2:216042927
|
T | TTA | 3 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0288 | 3 | HG02080.hp1 HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.826+975_826+976dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042927 | ||||||
chr2:216042949
|
G | A | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+955C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042949 | ||||||
chr2:216042949
|
G | GTGTATAT others(21): Show |
4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+954_826+955ins others(28): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042949 | ||||||
chr2:216042951
|
G | GTA | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+951_826+952dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042951 | ||||||
chr2:216042953
|
A | G | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+951T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042953 | ||||||
chr2:216042964
|
C | T | 14 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(11): Show | 14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+940G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042964 | ||||||
chr2:216042966
|
C | CAT | 4 | a0002c0002t0002g0366a0002c0002t0002g0367a0002c0002t0002g0369others(1): Show | 4 | HG02717.hp2 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+936_826+937dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042966 | ||||||
chr2:216042966
|
C | T | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+938G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042966 | ||||||
chr2:216042970
|
C | T | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+934G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042970 | ||||||
chr2:216042971
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(133): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.826+933C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042971 | ||||||
chr2:216042977
|
G | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+927C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042977 | ||||||
chr2:216042979
|
G | A | 14 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(11): Show | 14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+925C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | ||||||
chr2:216042979
|
G | GTA | 250 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.826+923_826+924dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | ||||||
chr2:216042979
|
G | GTATATAT others(23): Show |
2 | a0001c0004t0001g0089a0001c0004t0001g0090 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.826+924_826+925ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | ||||||
chr2:216042979
|
G | GTATATAT others(51): Show |
2 | a0002c0002t0002g0132a0002c0002t0002g0257 | 2 | NA18983.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.826+924_826+925ins others(58): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | ||||||
chr2:216042984
|
T | C | 2 | a0006c0005t0009g0217a0010c0012t0003g0215 | 2 | HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+920A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042984 | ||||||
chr2:216042988
|
T | C | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+916A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042988 | ||||||
chr2:216042988
|
T | TATATAC | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+915_826+916ins others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042988 | ||||||
chr2:216042990
|
T | C | 6 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+914A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042990 | ||||||
chr2:216042990
|
T | TAC | 12 | a0001c0001t0001g0268a0001c0001t0004g0312a0001c0001t0005g0313others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.826+912_826+913dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042990 | ||||||
chr2:216042994
|
T | C | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+910A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042994 | ||||||
chr2:216042996
|
C | T | 2 | a0006c0005t0009g0217a0010c0012t0003g0215 | 2 | HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+908G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042996 | ||||||
chr2:216042997
|
G | A | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+907C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042997 | ||||||
chr2:216043003
|
G | A | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+901C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043003 | ||||||
chr2:216043005
|
G | A | 11 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+899C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043005 | ||||||
chr2:216043007
|
A | G | 3 | a0001c0003t0003g0191a0001c0004t0001g0089a0006c0005t0009g0381 | 3 | HG02109.hp1 HG02647.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.826+897T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043007 | ||||||
chr2:216043016
|
T | C | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+888A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043016 | ||||||
chr2:216043016
|
T | TATACAC | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+887_826+888ins others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043016 | ||||||
chr2:216043019
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0036others(2): Show | 6 | NA18945.hp1 NA18961.hp2 NA19070.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+885T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043019 | ||||||
chr2:216043025
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.826+879C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043025 | ||||||
chr2:216043025
|
GTA | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+877_826+878del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043025 | ||||||
chr2:216043027
|
A | ATATGTGT others(23): Show |
1 | a0001c0001t0005g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826+876_826+877ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043027 | ||||||
chr2:216043031
|
A | G | 22 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(19): Show | 22 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+873T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043031 | ||||||
chr2:216043035
|
A | G | 14 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(11): Show | 14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+869T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043035 | ||||||
chr2:216043035
|
ATG | A | 225 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(222): Show | 231 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.826+867_826+868del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043035 | ||||||
chr2:216043037
|
G | A | 7 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(4): Show | 7 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+867C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043037 | ||||||
chr2:216043037
|
G | GTATATAT others(23): Show |
20 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0033others(17): Show | 22 | HG00280.hp2 HG00323.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+866_826+867ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043037 | ||||||
chr2:216043037
|
G | GTATATAT others(23): Show |
8 | a0001c0001t0004g0312a0001c0001t0005g0314a0001c0001t0005g0316others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.826+866_826+867ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043037 | ||||||
chr2:216043039
|
G | A | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+865C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043039 | ||||||
chr2:216043039
|
GTA | G | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(8): Show | 11 | HG02486.hp2 HG02572.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+863_826+864del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043039 | ||||||
chr2:216043049
|
ATACACAT others(3): Show |
A | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+845_826+854del others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043049 | ||||||
chr2:216043052
|
C | T | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+852G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043052 | ||||||
chr2:216043053
|
A | G | 3 | a0001c0001t0005g0386a0002c0002t0002g0339a0002c0002t0002g0342 | 3 | HG02280.hp2 NA19064.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.826+851T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043053 | ||||||
chr2:216043057
|
ACG | A | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+845_826+846del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043057 | ||||||
chr2:216043059
|
G | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+845C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043059 | ||||||
chr2:216043062
|
T | C | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+842A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043062 | ||||||
chr2:216043063
|
A | ACG | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+840_826+841ins others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043063 | ||||||
chr2:216043063
|
A | G | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+841T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043063 | ||||||
chr2:216043067
|
G | A | 2 | a0006c0005t0009g0381a0010c0012t0003g0215 | 2 | HG02109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.826+837C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043067 | ||||||
chr2:216043071
|
G | A | 13 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(10): Show | 13 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.826+833C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043071 | ||||||
chr2:216043071
|
G | GTA | 366 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(363): Show | 378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.826+831_826+832dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043071 | ||||||
chr2:216043071
|
G | GTGTA | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0082others(2): Show | 5 | HG02486.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+832_826+833ins others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043071 | ||||||
chr2:216043080
|
T | C | 1 | a0006c0005t0009g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.826+824A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043080 | ||||||
chr2:216043083
|
A | G | 6 | a0001c0001t0001g0053a0001c0001t0001g0085a0001c0001t0001g0199others(3): Show | 6 | HG01081.hp1 HG02040.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+821T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043083 | ||||||
chr2:216043084
|
C | CACATATA others(19): Show |
7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+819_826+820ins others(26): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043084 | ||||||
chr2:216043086
|
T | C | 11 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(8): Show | 11 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+818A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043086 | ||||||
chr2:216043088
|
C | T | 6 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+816G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043088 | ||||||
chr2:216043089
|
A | G | 3 | a0001c0001t0001g0199a0002c0002t0002g0365a0002c0002t0002g0380 | 3 | HG01884.hp2 HG03540.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.826+815T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043089 | ||||||
chr2:216043090
|
T | C | 9 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 9 | HG01975.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+814A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043090 | ||||||
chr2:216043091
|
A | G | 2 | a0006c0005t0009g0217a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.826+813T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043091 | ||||||
chr2:216043092
|
T | C | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+812A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043092 | ||||||
chr2:216043093
|
A | G | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+811T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043093 | ||||||
chr2:216043094
|
T | C | 1 | a0010c0012t0003g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.826+810A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043094 | ||||||
chr2:216043095
|
A | G | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+809T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043095 | ||||||
chr2:216043096
|
T | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(272): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.826+808A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043096 | ||||||
chr2:216043097
|
G | A | 1 | a0010c0012t0003g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.826+807C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043097 | ||||||
chr2:216043099
|
A | G | 1 | a0010c0012t0003g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.826+805T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043099 | ||||||
chr2:216043101
|
G | A | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+803C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043101 | ||||||
chr2:216043102
|
C | T | 32 | a0001c0001t0001g0020a0001c0001t0001g0155a0001c0001t0001g0212others(29): Show | 32 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.826+802G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043102 | ||||||
chr2:216043103
|
G | A | 34 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0057others(31): Show | 34 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.826+801C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043103 | ||||||
chr2:216043115
|
A | ATTTT | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+785_826+788dup others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043115 | ||||||
chr2:216043115
|
A | T | 9 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(6): Show | 9 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+789T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043115 | ||||||
chr2:216043117
|
T | A | 8 | a0001c0001t0001g0134a0001c0004t0001g0089a0001c0004t0001g0090others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+787A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043117 | ||||||
chr2:216043177
|
G | A | 1 | a0001c0001t0001g0003 | 2 | NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.826+727C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043177 | ||||||
chr2:216043198
|
C | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+706G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043198 | ||||||
chr2:216043284
|
A | AT | 14 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(11): Show | 14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+619dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043284 | ||||||
chr2:216043405
|
C | T | 1 | a0001c0001t0004g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.826+499G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043405 | ||||||
chr2:216043504
|
T | C | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+400A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043504 | ||||||
chr2:216043632
|
C | T | 4 | a0001c0001t0004g0262a0001c0001t0004g0266a0001c0001t0004g0373others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+272G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043632 | ||||||
chr2:216043704
|
C | T | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+200G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043704 | ||||||
chr2:216043711
|
T | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+193A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043711 | ||||||
chr2:216044055
|
T | A | 2 | a0002c0002t0002g0365a0002c0002t0002g0380 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.715-40A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044055 | ||||||
chr2:216044073
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.715-58C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044073 | ||||||
chr2:216044163
|
A | T | 3 | a0001c0003t0003g0190a0001c0003t0003g0192a0001c0003t0003g0193 | 3 | HG02132.hp1 NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.715-148T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044163 | ||||||
chr2:216044187
|
T | C | 280 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(277): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.715-172A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044187 | ||||||
chr2:216044200
|
C | G | 50 | a0002c0002t0002g0060a0002c0002t0002g0070a0002c0002t0002g0073others(47): Show | 50 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.715-185G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044200 | ||||||
chr2:216044254
|
G | A | 1 | a0009c0013t0002g0245 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.715-239C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044254 | ||||||
chr2:216044356
|
T | G | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-341A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044356 | ||||||
chr2:216044484
|
G | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-469C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044484 | ||||||
chr2:216044571
|
G | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-556C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044571 | ||||||
chr2:216044613
|
C | G | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-598G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044613 | ||||||
chr2:216044619
|
G | T | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-604C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044619 | ||||||
chr2:216044628
|
A | G | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-613T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044628 | ||||||
chr2:216044645
|
A | G | 280 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(277): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.715-630T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044645 | ||||||
chr2:216044702
|
AT | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-688delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044702 | ||||||
chr2:216044712
|
A | T | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-697T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044712 | ||||||
chr2:216044725
|
G | A | 1 | a0001c0003t0003g0200 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.715-710C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044725 | ||||||
chr2:216044792
|
C | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-777G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044792 | ||||||
chr2:216044858
|
G | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-843C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044858 | ||||||
chr2:216045120
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715-1105C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045120 | ||||||
chr2:216045149
|
C | G | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-1134G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045149 | ||||||
chr2:216045164
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-1149G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045164 | ||||||
chr2:216045179
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0140 | 2 | NA18949.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.715-1164T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045179 | ||||||
chr2:216045273
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.715-1258G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045273 | ||||||
chr2:216045308
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.715-1293C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045308 | ||||||
chr2:216045373
|
C | T | 1 | a0001c0001t0006g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.715-1358G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045373 | ||||||
chr2:216045454
|
A | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.715-1439T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045454 | ||||||
chr2:216045490
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0097others(6): Show | 10 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.715-1475G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045490 | ||||||
chr2:216045570
|
T | A | 3 | a0006c0005t0009g0217a0006c0005t0009g0381a0010c0012t0003g0215 | 3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-1555A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045570 | ||||||
chr2:216045747
|
G | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | NA18990.hp2 NA18993.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.715-1732C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045747 | ||||||
chr2:216045893
|
A | T | 1 | a0001c0003t0003g0011 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.715-1878T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045893 | ||||||
chr2:216046015
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0230others(1): Show | 4 | HG01346.hp1 HG02040.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-2000T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046015 | ||||||
chr2:216046039
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-2024A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046039 | ||||||
chr2:216046048
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.715-2033T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046048 | ||||||
chr2:216046101
|
CA | C | 9 | a0001c0001t0001g0180a0001c0001t0001g0349a0001c0001t0004g0266others(6): Show | 9 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-2087delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046101 | ||||||
chr2:216046276
|
GTA | G | 71 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(68): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-2263_715-2262d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046276 | ||||||
chr2:216046277
|
T | TATATATA others(7): Show |
1 | a0002c0002t0002g0101 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.715-2263_715-2262i others(16): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046277 | ||||||
chr2:216046283
|
T | TATACATA others(1): Show |
6 | a0002c0002t0002g0244a0002c0002t0002g0247a0002c0002t0002g0249others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-2269_715-2268i others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046283 | ||||||
chr2:216046285
|
T | TAC | 80 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0016others(77): Show | 83 | HG00544.hp2 HG00738.hp1 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-2271_715-2270i others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046285 | ||||||
chr2:216046285
|
T | TACATAC | 42 | a0001c0001t0001g0361a0001c0001t0004g0050a0002c0002t0002g0060others(39): Show | 42 | HG00597.hp2 HG01168.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.715-2271_715-2270i others(8): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046285 | ||||||
chr2:216046287
|
T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0027others(69): Show | 74 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.715-2272A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046287 | ||||||
chr2:216046289
|
C | CAT | 22 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0092others(19): Show | 23 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.715-2276_715-2275d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046289 | ||||||
chr2:216046289
|
C | T | 123 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0027others(120): Show | 125 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.715-2274G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046289 | ||||||
chr2:216046291
|
T | C | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0027others(68): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-2276A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046291 | ||||||
chr2:216046293
|
C | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(201): Show | 209 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.715-2278G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046293 | ||||||
chr2:216046302
|
A | T | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-2287T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046302 | ||||||
chr2:216046304
|
A | T | 2 | a0001c0011t0006g0383a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2289T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046304 | ||||||
chr2:216046306
|
A | T | 2 | a0001c0011t0006g0383a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2291T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046306 | ||||||
chr2:216046308
|
A | T | 3 | a0001c0001t0001g0214a0001c0011t0006g0383a0006c0005t0009g0381 | 3 | HG02109.hp1 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2293T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046308 | ||||||
chr2:216046310
|
A | AT | 10 | a0001c0001t0001g0083a0001c0001t0001g0216a0001c0003t0003g0146others(7): Show | 10 | HG01256.hp2 HG02132.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-2296dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0097 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.715-2296_715-2295i others(17): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0329a0001c0001t0001g0330 | 4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-2296_715-2295i others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
A | ATATT | 8 | a0001c0001t0004g0157a0001c0001t0004g0158a0001c0001t0004g0352others(5): Show | 8 | HG02486.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-2296_715-2295i others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
A | ATT | 33 | a0001c0001t0004g0374a0001c0001t0006g0099a0001c0003t0001g0198others(30): Show | 34 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.715-2297_715-2296d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
A | G | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-2295T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
A | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0034others(15): Show | 19 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.715-2295T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046310
|
AT | A | 12 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0120others(9): Show | 12 | HG01891.hp2 HG02015.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-2296delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | ||||||
chr2:216046311
|
T | TA | 31 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0084others(28): Show | 33 | HG00280.hp2 HG01099.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.715-2297_715-2296i others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046311 | ||||||
chr2:216046311
|
T | TATATA | 3 | a0002c0002t0002g0229a0002c0002t0002g0240a0002c0002t0002g0371 | 3 | HG03654.hp2 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.715-2297_715-2296i others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046311 | ||||||
chr2:216046312
|
T | A | 125 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(122): Show | 128 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.715-2297A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046312 | ||||||
chr2:216046313
|
T | A | 25 | a0001c0001t0001g0058a0001c0001t0001g0082a0001c0001t0001g0084others(22): Show | 26 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.715-2298A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046313 | ||||||
chr2:216046313
|
T | G | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.715-2298A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046313 | ||||||
chr2:216046314
|
T | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0182a0001c0001t0001g0267others(8): Show | 11 | HG00609.hp2 HG02080.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-2299A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046314 | ||||||
chr2:216046314
|
T | G | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-2299A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046314 | ||||||
chr2:216046315
|
T | A | 6 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0317others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-2300A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046315 | ||||||
chr2:216046318
|
T | G | 2 | a0001c0011t0006g0383a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2303A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046318 | ||||||
chr2:216046323
|
T | G | 2 | a0001c0011t0006g0383a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2308A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046323 | ||||||
chr2:216046323
|
T | TTTTTGTT others(3): Show |
1 | a0010c0012t0003g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.715-2309_715-2308i others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046323 | ||||||
chr2:216046339
|
G | A | 87 | a0001c0001t0006g0099a0002c0002t0002g0010a0002c0002t0002g0018others(84): Show | 88 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.715-2324C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046339 | ||||||
chr2:216046500
|
C | T | 1 | a0001c0003t0003g0301 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.715-2485G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046500 | ||||||
chr2:216046510
|
C | T | 1 | a0002c0002t0010g0336 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.715-2495G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046510 | ||||||
chr2:216046617
|
A | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-2602T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046617 | ||||||
chr2:216046674
|
A | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0384a0001c0001t0007g0074others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+2589T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046674 | ||||||
chr2:216046759
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0243 | 2 | HG02040.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.714+2504A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046759 | ||||||
chr2:216046922
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.714+2341G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046922 | ||||||
chr2:216047118
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2145A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047118 | ||||||
chr2:216047259
|
A | AG | 3 | a0001c0001t0004g0266a0001c0001t0004g0373a0001c0001t0004g0374 | 3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.714+2003dupC | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047259 | ||||||
chr2:216047260
|
G | GAA | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2002_714+2003i others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047260 | ||||||
chr2:216047261
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2002C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047261 | ||||||
chr2:216047261
|
G | GA | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(264): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.714+2001dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047261 | ||||||
chr2:216047512
|
C | A | 1 | a0002c0002t0002g0380 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.714+1751G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047512 | ||||||
chr2:216047719
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1544G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047719 | ||||||
chr2:216047756
|
CA | C | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.714+1506delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047756 | ||||||
chr2:216047781
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.714+1482C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047781 | ||||||
chr2:216047810
|
A | ATAAAT | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1452_714+1453i others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047810 | ||||||
chr2:216047827
|
G | A | 3 | a0001c0001t0004g0266a0001c0001t0004g0373a0001c0001t0004g0374 | 3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.714+1436C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047827 | ||||||
chr2:216047842
|
T | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.714+1421A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047842 | ||||||
chr2:216047897
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1366A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047897 | ||||||
chr2:216047983
|
A | AT | 14 | a0001c0001t0001g0035a0001c0001t0004g0266a0001c0001t0004g0312others(11): Show | 14 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.714+1279dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047983 | ||||||
chr2:216047983
|
AT | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(78): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.714+1279delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047983 | ||||||
chr2:216048013
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.714+1250A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048013 | ||||||
chr2:216048057
|
C | CTTTTCTT | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1199_714+1205d others(9): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048057 | ||||||
chr2:216048067
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1196G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048067 | ||||||
chr2:216048075
|
T | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1188A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048075 | ||||||
chr2:216048107
|
C | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0373a0001c0001t0004g0374 | 3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.714+1156G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048107 | ||||||
chr2:216048131
|
G | A | 1 | a0001c0001t0005g0386 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.714+1132C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048131 | ||||||
chr2:216048133
|
G | A | 10 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.714+1130C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048133 | ||||||
chr2:216048135
|
T | C | 5 | a0001c0001t0004g0354a0001c0011t0006g0383a0006c0005t0009g0217others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+1128A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048135 | ||||||
chr2:216048187
|
G | C | 2 | a0002c0002t0002g0125a0002c0002t0002g0238 | 2 | NA18612.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.714+1076C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048187 | ||||||
chr2:216048221
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1042A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048221 | ||||||
chr2:216048235
|
C | T | 13 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.714+1028G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048235 | ||||||
chr2:216048277
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.714+986C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048277 | ||||||
chr2:216048311
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+952C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048311 | ||||||
chr2:216048326
|
C | T | 3 | a0001c0001t0007g0074a0001c0001t0007g0075a0001c0001t0007g0079 | 3 | HG01106.hp2 HG01358.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.714+937G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048326 | ||||||
chr2:216048333
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+930G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048333 | ||||||
chr2:216048344
|
G | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0384a0001c0001t0007g0074others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+919C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048344 | ||||||
chr2:216048366
|
C | T | 16 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0004g0050others(13): Show | 16 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.714+897G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048366 | ||||||
chr2:216048368
|
C | A | 1 | a0002c0002t0002g0328 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.714+895G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048368 | ||||||
chr2:216048384
|
TA | T | 231 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(228): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.714+878delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048384 | ||||||
chr2:216048384
|
TAA | T | 34 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0147others(31): Show | 34 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.714+877_714+878del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048384 | ||||||
chr2:216048441
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0295 | 2 | HG01516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.714+822C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048441 | ||||||
chr2:216048464
|
C | T | 2 | a0002c0002t0002g0365a0002c0002t0002g0380 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.714+799G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048464 | ||||||
chr2:216048485
|
G | GT | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+777dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048485 | ||||||
chr2:216048584
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+679A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048584 | ||||||
chr2:216048625
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0097a0001c0001t0001g0329others(1): Show | 5 | HG02055.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+638C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048625 | ||||||
chr2:216048645
|
A | G | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(276): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.714+618T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048645 | ||||||
chr2:216048650
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0218 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.714+613G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048650 | ||||||
chr2:216048730
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0121others(12): Show | 16 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+533C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048730 | ||||||
chr2:216048843
|
C | CA | 42 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(39): Show | 43 | HG00558.hp2 HG00642.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.714+419dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048843 | ||||||
chr2:216048843
|
C | CAA | 11 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0065others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+418_714+419dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048843 | ||||||
chr2:216048843
|
CA | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(172): Show | 182 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.714+419delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048843 | ||||||
chr2:216048865
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+398T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048865 | ||||||
chr2:216048869
|
G | A | 25 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0004g0050others(22): Show | 25 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.714+394C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048869 | ||||||
chr2:216048888
|
G | C | 1 | a0001c0001t0006g0099 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.714+375C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048888 | ||||||
chr2:216048957
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+306T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048957 | ||||||
chr2:216049064
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+199T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216049064 | ||||||
chr2:216049090
|
G | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0097others(6): Show | 10 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.714+173C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216049090 | ||||||
chr2:216049185
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.714+78C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216049185 | ||||||
chr2:216049763
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG03831.hp2 NA20752.hp2 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.604-390G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216049763 | ||||||
chr2:216049947
|
G | A | 16 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0004g0050others(13): Show | 16 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.604-574C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216049947 | ||||||
chr2:216050018
|
G | C | 1 | a0002c0002t0002g0328 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.604-645C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050018 | ||||||
chr2:216050155
|
G | A | 1 | a0001c0001t0004g0357 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.604-782C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050155 | ||||||
chr2:216050197
|
A | G | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(277): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.604-824T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050197 | ||||||
chr2:216050303
|
G | A | 3 | a0001c0003t0003g0186a0001c0003t0003g0187a0007c0008t0002g0259 | 3 | HG01515.hp2 HG01517.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.604-930C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050303 | ||||||
chr2:216050416
|
T | C | 1 | a0001c0001t0001g0382 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.603+1033A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050416 | ||||||
chr2:216050858
|
G | A | 1 | a0002c0002t0002g0153 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.603+591C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050858 | ||||||
chr2:216050899
|
T | TA | 13 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0097others(10): Show | 13 | HG00423.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.603+549dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050899 | ||||||
chr2:216050899
|
TA | T | 11 | a0001c0001t0001g0046a0001c0001t0001g0270a0001c0001t0004g0312others(8): Show | 11 | HG01168.hp2 HG01257.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.603+549delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050899 | ||||||
chr2:216051084
|
G | A | 1 | a0001c0003t0003g0207 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603+365C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051084 | ||||||
chr2:216051095
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0097others(6): Show | 10 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.603+354C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051095 | ||||||
chr2:216051099
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.603+350T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051099 | ||||||
chr2:216051115
|
A | G | 270 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(267): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.603+334T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051115 | ||||||
chr2:216051275
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.603+174G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051275 | ||||||
chr2:216051281
|
C | CAAA | 6 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG01975.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+165_603+167dup others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | ||||||
chr2:216051281
|
CA | C | 112 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0024others(109): Show | 114 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(111): Show |
intron_variant | MODIFIER | c.603+167delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | ||||||
chr2:216051281
|
CAA | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0066others(80): Show | 85 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.603+166_603+167del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | ||||||
chr2:216051281
|
CAAA | C | 78 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0016others(75): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.603+165_603+167del others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | ||||||
chr2:216051299
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0004g0312a0001c0001t0005g0324 | 3 | HG02818.hp2 HG03041.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.603+150T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051299 | ||||||
chr2:216051813
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-268T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216051813 | ||||||
chr2:216051962
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.507-417C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216051962 | ||||||
chr2:216052034
|
A | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-489T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052034 | ||||||
chr2:216052051
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.507-506A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052051 | ||||||
chr2:216052058
|
T | C | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(276): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.507-513A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052058 | ||||||
chr2:216052075
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-530C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052075 | ||||||
chr2:216052100
|
C | T | 1 | a0001c0001t0005g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507-555G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052100 | ||||||
chr2:216052101
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-556C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052101 | ||||||
chr2:216052218
|
T | C | 1 | a0002c0002t0002g0300 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.507-673A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052218 | ||||||
chr2:216052287
|
A | G | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | NA18990.hp2 NA18993.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.507-742T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052287 | ||||||
chr2:216052572
|
T | C | 1 | a0002c0002t0002g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.507-1027A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052572 | ||||||
chr2:216052575
|
T | C | 3 | a0001c0001t0001g0360a0001c0001t0006g0023a0001c0001t0006g0099 | 3 | HG02145.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.507-1030A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052575 | ||||||
chr2:216052635
|
C | T | 1 | a0002c0002t0010g0336 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.507-1090G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052635 | ||||||
chr2:216052646
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.507-1101C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052646 | ||||||
chr2:216052675
|
T | G | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-1130A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052675 | ||||||
chr2:216052823
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.507-1278G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052823 | ||||||
chr2:216052832
|
C | G | 2 | a0002c0002t0002g0367a0002c0002t0002g0369 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.507-1287G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052832 | ||||||
chr2:216052841
|
C | G | 2 | a0001c0001t0001g0360a0001c0001t0006g0099 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.507-1296G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052841 | ||||||
chr2:216052891
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0243 | 2 | HG02040.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.507-1346A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052891 | ||||||
chr2:216052922
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.507-1377G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052922 | ||||||
chr2:216052986
|
T | C | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-1441A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052986 | ||||||
chr2:216053080
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0035 | 3 | NA18960.hp1 NA18980.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.507-1535G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053080 | ||||||
chr2:216053103
|
C | T | 3 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0385 | 3 | HG02145.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.507-1558G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053103 | ||||||
chr2:216053236
|
A | ATTTTG | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-1696_507-1692d others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053236 | ||||||
chr2:216053236
|
ATTTTG | A | 15 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.507-1696_507-1692d others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053236 | ||||||
chr2:216053446
|
G | A | 256 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(253): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.507-1901C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053446 | ||||||
chr2:216054284
|
T | C | 1 | a0002c0002t0002g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.507-2739A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054284 | ||||||
chr2:216054306
|
A | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0302 | 2 | HG00438.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.507-2761T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054306 | ||||||
chr2:216054339
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.507-2794C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054339 | ||||||
chr2:216054364
|
T | C | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.507-2819A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054364 | ||||||
chr2:216054371
|
C | CT | 8 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0051others(5): Show | 8 | HG00609.hp1 HG00741.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-2827dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | ||||||
chr2:216054371
|
CT | C | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(242): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.507-2827delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | ||||||
chr2:216054371
|
CTTTTTTT | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-2833_507-2827d others(9): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | ||||||
chr2:216054371
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-2835_507-2827d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | ||||||
chr2:216054670
|
T | C | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.507-3125A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054670 | ||||||
chr2:216054682
|
A | G | 1 | a0002c0002t0002g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.507-3137T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054682 | ||||||
chr2:216054748
|
T | C | 1 | a0002c0002t0002g0371 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.507-3203A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054748 | ||||||
chr2:216054749
|
T | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-3204A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054749 | ||||||
chr2:216054888
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.507-3343C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054888 | ||||||
chr2:216054980
|
C | A | 1 | a0002c0002t0002g0240 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.507-3435G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054980 | ||||||
chr2:216054984
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.507-3439G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054984 | ||||||
chr2:216055113
|
C | CA | 6 | a0001c0001t0001g0049a0001c0001t0001g0067a0001c0001t0008g0278others(3): Show | 6 | HG01981.hp2 HG02293.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.507-3569dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055113 | ||||||
chr2:216055113
|
C | CAA | 8 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-3570_507-3569d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055113 | ||||||
chr2:216055115
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.507-3570T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055115 | ||||||
chr2:216055146
|
A | T | 1 | a0001c0001t0005g0219 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.507-3601T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055146 | ||||||
chr2:216055375
|
T | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(253): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.506+3520A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055375 | ||||||
chr2:216055403
|
C | G | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(137): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.506+3492G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055403 | ||||||
chr2:216055423
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+3472T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055423 | ||||||
chr2:216055433
|
A | G | 275 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(272): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.506+3462T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055433 | ||||||
chr2:216055434
|
T | C | 1 | a0001c0001t0005g0386 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.506+3461A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055434 | ||||||
chr2:216055437
|
CA | C | 264 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(261): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.506+3457delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055437 | ||||||
chr2:216055441
|
AAAAAAAA others(2): Show |
A | 10 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.506+3445_506+3453d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055441 | ||||||
chr2:216055443
|
A | C | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.506+3452T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055443 | ||||||
chr2:216055462
|
A | C | 18 | a0001c0001t0001g0137a0001c0001t0001g0285a0001c0001t0001g0361others(15): Show | 19 | HG00423.hp2 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.506+3433T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055462 | ||||||
chr2:216055500
|
A | C | 2 | a0001c0001t0004g0312a0001c0001t0005g0324 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.506+3395T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055500 | ||||||
chr2:216055530
|
GACA | G | 10 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(7): Show | 10 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.506+3362_506+3364d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055530 | ||||||
chr2:216055859
|
G | T | 1 | a0001c0001t0001g0134 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.506+3036C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055859 | ||||||
chr2:216055992
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2903G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055992 | ||||||
chr2:216056116
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2779T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056116 | ||||||
chr2:216056119
|
C | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2776G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056119 | ||||||
chr2:216056189
|
C | T | 1 | a0001c0001t0001g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.506+2706G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056189 | ||||||
chr2:216056342
|
C | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0384a0001c0001t0007g0074others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+2553G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056342 | ||||||
chr2:216056467
|
T | A | 4 | a0001c0003t0003g0093a0001c0003t0003g0183a0001c0003t0003g0185others(1): Show | 4 | HG00733.hp1 HG00741.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+2428A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056467 | ||||||
chr2:216056550
|
G | A | 256 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(253): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.506+2345C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056550 | ||||||
chr2:216056585
|
G | A | 2 | a0001c0001t0006g0023a0001c0001t0006g0099 | 2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.506+2310C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056585 | ||||||
chr2:216056599
|
C | T | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(276): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.506+2296G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056599 | ||||||
chr2:216056697
|
G | A | 4 | a0001c0001t0001g0296a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+2198C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056697 | ||||||
chr2:216056721
|
CAGAAAAA others(4): Show |
C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2163_506+2173d others(13): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056721 | ||||||
chr2:216056723
|
G | GA | 92 | a0001c0001t0001g0035a0001c0001t0001g0130a0001c0001t0004g0266others(89): Show | 93 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.506+2171dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056723 | ||||||
chr2:216056796
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2099C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056796 | ||||||
chr2:216056821
|
T | C | 6 | a0001c0001t0001g0284a0001c0001t0001g0295a0001c0011t0006g0383others(3): Show | 6 | HG01516.hp2 HG02109.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+2074A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056821 | ||||||
chr2:216056889
|
A | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2006T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056889 | ||||||
chr2:216056895
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.506+2000G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056895 | ||||||
chr2:216056897
|
G | T | 1 | a0001c0001t0007g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.506+1998C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056897 | ||||||
chr2:216056909
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.506+1986C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056909 | ||||||
chr2:216056938
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.506+1957A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056938 | ||||||
chr2:216057031
|
T | C | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.506+1864A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057031 | ||||||
chr2:216057168
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.506+1727G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057168 | ||||||
chr2:216057206
|
A | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+1689T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057206 | ||||||
chr2:216057235
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0290 | 3 | HG02015.hp2 HG02129.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.506+1660G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057235 | ||||||
chr2:216057489
|
G | T | 20 | a0001c0001t0001g0361a0001c0001t0004g0050a0001c0001t0004g0156others(17): Show | 20 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.506+1406C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057489 | ||||||
chr2:216057512
|
A | G | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+1383T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057512 | ||||||
chr2:216057636
|
G | T | 1 | a0002c0002t0002g0366 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506+1259C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057636 | ||||||
chr2:216057869
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG00280.hp2 HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.506+1026A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057869 | ||||||
chr2:216058042
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.506+853T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058042 | ||||||
chr2:216058084
|
T | C | 1 | a0001c0001t0004g0357 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.506+811A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058084 | ||||||
chr2:216058152
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+743G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058152 | ||||||
chr2:216058182
|
T | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+713A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058182 | ||||||
chr2:216058386
|
G | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+509C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058386 | ||||||
chr2:216058410
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.506+485C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058410 | ||||||
chr2:216058478
|
A | T | 1 | a0002c0002t0002g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.506+417T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058478 | ||||||
chr2:216058574
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+321A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058574 | ||||||
chr2:216058830
|
A | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+65T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058830 | ||||||
chr2:216059166
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0133a0001c0001t0001g0136others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-190A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059166 | ||||||
chr2:216059222
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0109a0001c0001t0001g0120others(6): Show | 10 | NA18941.hp2 NA18949.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-246G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059222 | ||||||
chr2:216059301
|
G | T | 3 | a0001c0001t0004g0266a0001c0001t0004g0373a0001c0001t0004g0374 | 3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.425-325C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059301 | ||||||
chr2:216059351
|
C | T | 1 | a0002c0002t0002g0132 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.425-375G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059351 | ||||||
chr2:216059416
|
T | A | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.425-440A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059416 | ||||||
chr2:216059424
|
T | C | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.425-448A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059424 | ||||||
chr2:216059442
|
C | T | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-466G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059442 | ||||||
chr2:216059537
|
T | C | 3 | a0001c0001t0001g0360a0001c0001t0006g0023a0001c0001t0006g0099 | 3 | HG02145.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.425-561A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059537 | ||||||
chr2:216059617
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-641G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059617 | ||||||
chr2:216059769
|
C | T | 2 | a0001c0004t0001g0089a0001c0004t0001g0090 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.425-793G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059769 | ||||||
chr2:216059922
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG00280.hp2 HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.425-946A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059922 | ||||||
chr2:216060049
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.425-1073G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060049 | ||||||
chr2:216060244
|
C | T | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1268G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060244 | ||||||
chr2:216060248
|
C | T | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1272G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060248 | ||||||
chr2:216060280
|
T | C | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | NA18943.hp1 NA18969.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-1304A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060280 | ||||||
chr2:216060371
|
A | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-1395T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060371 | ||||||
chr2:216060479
|
G | C | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1503C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060479 | ||||||
chr2:216060528
|
G | A | 2 | a0002c0002t0002g0365a0002c0002t0002g0380 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.425-1552C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060528 | ||||||
chr2:216060539
|
A | G | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1563T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060539 | ||||||
chr2:216060608
|
G | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-1632C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060608 | ||||||
chr2:216060613
|
T | C | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.425-1637A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060613 | ||||||
chr2:216060742
|
C | T | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1766G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060742 | ||||||
chr2:216060743
|
A | C | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1767T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060743 | ||||||
chr2:216060755
|
T | A | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1779A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060755 | ||||||
chr2:216060766
|
C | T | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1790G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060766 | ||||||
chr2:216060771
|
A | C | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1795T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060771 | ||||||
chr2:216060818
|
A | T | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1842T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060818 | ||||||
chr2:216060837
|
A | T | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1861T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060837 | ||||||
chr2:216060843
|
A | T | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1867T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060843 | ||||||
chr2:216060845
|
A | C | 1 | a0001c0001t0008g0293 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1869T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060845 | ||||||
chr2:216060874
|
GA | G | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1899delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060874 | ||||||
chr2:216060921
|
TAATA | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0097others(5): Show | 9 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-1949_425-1946d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060921 | ||||||
chr2:216061092
|
G | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-2116C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061092 | ||||||
chr2:216061129
|
C | CA | 14 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0036others(11): Show | 14 | HG00423.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.425-2154dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | ||||||
chr2:216061129
|
CA | C | 50 | a0001c0001t0001g0024a0001c0001t0001g0096a0001c0001t0001g0097others(47): Show | 50 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.425-2154delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | ||||||
chr2:216061129
|
CAA | C | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(204): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.425-2155_425-2154d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | ||||||
chr2:216061129
|
CAAA | C | 14 | a0001c0001t0001g0161a0001c0001t0001g0218a0001c0001t0001g0360others(11): Show | 14 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.425-2156_425-2154d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | ||||||
chr2:216061131
|
A | C | 2 | a0001c0011t0006g0383a0006c0005t0009g0217 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.425-2155T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061131 | ||||||
chr2:216061132
|
A | C | 2 | a0006c0005t0009g0381a0010c0012t0003g0215 | 2 | HG02109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.425-2156T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061132 | ||||||
chr2:216061188
|
T | C | 4 | a0001c0001t0001g0103a0001c0001t0001g0145a0001c0001t0001g0161others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2212A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061188 | ||||||
chr2:216061258
|
G | A | 2 | a0001c0001t0004g0358a0001c0001t0004g0359 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-2282C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061258 | ||||||
chr2:216061263
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.425-2287C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061263 | ||||||
chr2:216061276
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2300G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061276 | ||||||
chr2:216061311
|
C | CA | 36 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0017others(33): Show | 37 | HG00423.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.425-2336dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
C | CAA | 6 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0068others(3): Show | 6 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-2337_425-2336d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CA | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0087a0001c0001t0004g0315others(6): Show | 9 | HG01167.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-2336delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAA | C | 9 | a0001c0001t0001g0212a0001c0001t0001g0375a0001c0001t0004g0312others(6): Show | 9 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-2337_425-2336d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAA | C | 22 | a0001c0001t0001g0155a0001c0001t0001g0165a0001c0001t0001g0177others(19): Show | 23 | HG01167.hp2 HG01169.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.425-2338_425-2336d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAA | C | 66 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0084others(63): Show | 67 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.425-2339_425-2336d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAAA | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.425-2340_425-2336d others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAAAAA | C | 6 | a0002c0002t0002g0060a0002c0002t0002g0122a0002c0002t0002g0239others(3): Show | 6 | HG00597.hp2 HG01255.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-2342_425-2336d others(9): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAAAAA others(1): Show |
C | 49 | a0001c0011t0006g0383a0002c0002t0002g0070a0002c0002t0002g0101others(46): Show | 49 | HG00609.hp2 HG01168.hp1 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.425-2343_425-2336d others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAAAAA others(2): Show |
C | 34 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0073others(31): Show | 35 | HG00544.hp2 HG01109.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.425-2344_425-2336d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAAAAA others(3): Show |
C | 4 | a0002c0002t0002g0175a0002c0002t0002g0376a0002c0002t0002g0378others(1): Show | 4 | HG01070.hp2 HG01884.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-2345_425-2336d others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061311
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.425-2348_425-2336d others(15): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | ||||||
chr2:216061334
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0004g0266a0001c0001t0004g0373a0001c0001t0004g0374 | 3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.425-2368_425-2359d others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061334 | ||||||
chr2:216061343
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.425-2367T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061343 | ||||||
chr2:216061348
|
C | G | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.425-2372G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061348 | ||||||
chr2:216061349
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2373G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061349 | ||||||
chr2:216061491
|
G | A | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-2515C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061491 | ||||||
chr2:216061748
|
A | T | 385 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(382): Show | 397 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(394): Show |
intron_variant | MODIFIER | c.425-2772T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061748 | ||||||
chr2:216061790
|
T | C | 1 | a0001c0003t0003g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.425-2814A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061790 | ||||||
chr2:216061897
|
G | T | 1 | a0001c0003t0003g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.425-2921C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061897 | ||||||
chr2:216061955
|
C | T | 2 | a0001c0001t0001g0360a0001c0001t0006g0099 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.425-2979G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061955 | ||||||
chr2:216061970
|
A | ATGTG | 88 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(85): Show | 89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.425-2998_425-2995d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061970 | ||||||
chr2:216061970
|
A | ATGTGTGT others(3): Show |
3 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381 | 3 | HG02109.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.425-3004_425-2995d others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061970 | ||||||
chr2:216061970
|
A | ATGTGTGT others(7): Show |
1 | a0010c0012t0003g0215 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-3008_425-2995d others(16): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061970 | ||||||
chr2:216062040
|
A | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-3064T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062040 | ||||||
chr2:216062045
|
G | A | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-3069C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062045 | ||||||
chr2:216062052
|
A | AT | 8 | a0001c0001t0001g0049a0001c0001t0001g0163a0001c0001t0001g0346others(5): Show | 8 | HG01891.hp2 HG01981.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-3077dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062052 | ||||||
chr2:216062125
|
A | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-3149T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062125 | ||||||
chr2:216062236
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.424+3076C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062236 | ||||||
chr2:216062297
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0052a0001c0001t0001g0085others(8): Show | 12 | HG02015.hp1 HG02083.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+3015G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062297 | ||||||
chr2:216062441
|
G | A | 89 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(86): Show | 90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.424+2871C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062441 | ||||||
chr2:216062498
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.424+2814A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062498 | ||||||
chr2:216062543
|
T | C | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2769A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062543 | ||||||
chr2:216062639
|
G | A | 5 | a0002c0002t0002g0101a0002c0002t0002g0244a0002c0002t0002g0247others(2): Show | 5 | HG00609.hp2 NA18965.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2673C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062639 | ||||||
chr2:216062724
|
C | T | 87 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(84): Show | 88 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.424+2588G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062724 | ||||||
chr2:216062869
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+2443G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062869 | ||||||
chr2:216063075
|
T | C | 87 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0060others(84): Show | 88 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.424+2237A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063075 | ||||||
chr2:216063107
|
TA | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2204delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063107 | ||||||
chr2:216063142
|
A | C | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2170T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063142 | ||||||
chr2:216063225
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2087C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063225 | ||||||
chr2:216063239
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2073G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063239 | ||||||
chr2:216063243
|
T | C | 1 | a0002c0002t0002g0328 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+2069A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063243 | ||||||
chr2:216063444
|
C | T | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+1868G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063444 | ||||||
chr2:216063532
|
T | C | 93 | a0001c0011t0006g0383a0002c0002t0002g0010a0002c0002t0002g0018others(90): Show | 94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.424+1780A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063532 | ||||||
chr2:216063719
|
T | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1593A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063719 | ||||||
chr2:216063732
|
T | G | 2 | a0001c0001t0001g0360a0001c0001t0006g0099 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.424+1580A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063732 | ||||||
chr2:216063819
|
G | T | 1 | a0001c0001t0001g0292 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.424+1493C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063819 | ||||||
chr2:216063827
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.424+1485G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063827 | ||||||
chr2:216063889
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+1423A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063889 | ||||||
chr2:216063914
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1398C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063914 | ||||||
chr2:216063925
|
G | A | 8 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0283others(5): Show | 8 | HG00438.hp1 HG00544.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+1387C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063925 | ||||||
chr2:216063968
|
G | A | 5 | a0001c0001t0004g0156a0001c0001t0004g0157a0001c0001t0004g0158others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+1344C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063968 | ||||||
chr2:216063990
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.424+1322C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063990 | ||||||
chr2:216064042
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1270A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064042 | ||||||
chr2:216064138
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1174G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064138 | ||||||
chr2:216064147
|
C | T | 115 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(112): Show | 116 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.424+1165G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064147 | ||||||
chr2:216064201
|
A | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1111T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064201 | ||||||
chr2:216064243
|
A | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1069T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064243 | ||||||
chr2:216064336
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0039others(5): Show | 8 | HG02109.hp1 HG03486.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+976G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064336 | ||||||
chr2:216064399
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+913G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064399 | ||||||
chr2:216064557
|
T | G | 1 | a0001c0003t0003g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.424+755A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064557 | ||||||
chr2:216064560
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+752G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064560 | ||||||
chr2:216064885
|
T | G | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.424+427A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064885 | ||||||
chr2:216065228
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG02559.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+84C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216065228 | ||||||
chr2:216065523
|
C | T | 1 | a0001c0003t0003g0241 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.259-46G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065523 | ||||||
chr2:216065761
|
C | T | 6 | a0001c0003t0003g0190a0001c0003t0003g0191a0001c0003t0003g0192others(3): Show | 6 | HG02071.hp1 HG02132.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-284G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065761 | ||||||
chr2:216065765
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.259-288A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065765 | ||||||
chr2:216065852
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-375G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065852 | ||||||
chr2:216065942
|
C | T | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(270): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.258+443G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065942 | ||||||
chr2:216065943
|
G | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+442C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065943 | ||||||
chr2:216065952
|
C | T | 2 | a0002c0002t0002g0229a0002c0002t0002g0240 | 2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.258+433G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065952 | ||||||
chr2:216065961
|
G | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+424C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065961 | ||||||
chr2:216065967
|
T | C | 6 | a0001c0001t0001g0105a0001c0001t0001g0147a0001c0001t0001g0163others(3): Show | 6 | HG00438.hp2 HG00673.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+418A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065967 | ||||||
chr2:216066059
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+326C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066059 | ||||||
chr2:216066075
|
T | C | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+310A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066075 | ||||||
chr2:216066125
|
AAAAAAT | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+254_258+259del others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066125 | ||||||
chr2:216066151
|
T | TA | 5 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0385others(2): Show | 5 | HG02145.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+233dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066151 | ||||||
chr2:216066216
|
T | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+169A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066216 | ||||||
chr2:216066222
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+163C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066222 | ||||||
chr2:216066537
|
AGAACAAA others(59): Show |
A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-85_125-20delCC others(64): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066537 | ||||||
chr2:216066633
|
C | A | 2 | a0001c0001t0001g0360a0001c0001t0006g0099 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.125-115G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066633 | ||||||
chr2:216066865
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-347T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066865 | ||||||
chr2:216066897
|
G | C | 5 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0385others(2): Show | 5 | HG02145.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-379C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066897 | ||||||
chr2:216067004
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-486A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067004 | ||||||
chr2:216067059
|
T | C | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-541A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067059 | ||||||
chr2:216067065
|
C | G | 25 | a0002c0002t0002g0010a0002c0002t0002g0018a0002c0002t0002g0092others(22): Show | 26 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.125-547G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067065 | ||||||
chr2:216067184
|
T | TTGCCCAG others(4): Show |
1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-677_125-667dup others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067184 | ||||||
chr2:216067213
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.125-695G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067213 | ||||||
chr2:216067221
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-703C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067221 | ||||||
chr2:216067235
|
T | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-717A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067235 | ||||||
chr2:216067369
|
GCCCACCA others(7): Show |
G | 1 | a0001c0001t0001g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.125-865_125-852del others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067369 | ||||||
chr2:216067447
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.125-929G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067447 | ||||||
chr2:216067563
|
CT | C | 26 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0105others(23): Show | 26 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.125-1046delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067563 | ||||||
chr2:216067589
|
A | G | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1071T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067589 | ||||||
chr2:216067605
|
G | A | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(164): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.125-1087C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067605 | ||||||
chr2:216067625
|
C | T | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1107G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067625 | ||||||
chr2:216067993
|
C | T | 7 | a0001c0001t0001g0155a0001c0001t0001g0212a0001c0001t0001g0213others(4): Show | 7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-1475G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067993 | ||||||
chr2:216067996
|
A | T | 2 | a0001c0004t0001g0089a0001c0004t0001g0090 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.125-1478T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067996 | ||||||
chr2:216067999
|
C | A | 6 | a0002c0002t0002g0101a0002c0002t0002g0244a0002c0002t0002g0246others(3): Show | 6 | HG00609.hp2 HG04228.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-1481G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067999 | ||||||
chr2:216068155
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.125-1637T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068155 | ||||||
chr2:216068156
|
G | A | 6 | a0002c0002t0002g0108a0002c0002t0002g0111a0002c0002t0002g0112others(3): Show | 6 | NA18948.hp2 NA18961.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-1638C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068156 | ||||||
chr2:216068221
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0297others(1): Show | 4 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1703T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068221 | ||||||
chr2:216068225
|
C | CA | 49 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0033others(46): Show | 49 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.125-1708dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068225 | ||||||
chr2:216068225
|
CA | C | 132 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0016others(129): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.125-1708delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068225 | ||||||
chr2:216068225
|
CAA | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0097a0001c0001t0001g0155others(23): Show | 27 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.125-1709_125-1708d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068225 | ||||||
chr2:216068250
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.125-1732G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068250 | ||||||
chr2:216068701
|
G | A | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-2183C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068701 | ||||||
chr2:216068748
|
C | T | 9 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-2230G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068748 | ||||||
chr2:216068769
|
C | G | 3 | a0001c0001t0004g0266a0001c0001t0004g0373a0001c0001t0004g0374 | 3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.125-2251G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068769 | ||||||
chr2:216068804
|
A | AT | 16 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 16 | HG00673.hp1 HG01261.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-2287dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | ||||||
chr2:216068804
|
AT | A | 232 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(229): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.125-2287delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | ||||||
chr2:216068804
|
ATT | A | 17 | a0001c0001t0001g0147a0001c0001t0001g0218a0001c0001t0001g0294others(14): Show | 17 | HG01256.hp2 HG02109.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-2288_125-2287d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | ||||||
chr2:216068804
|
ATTTTTTT others(6): Show |
A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-2299_125-2287d others(15): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | ||||||
chr2:216068890
|
T | C | 1 | a0001c0001t0006g0023 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-2372A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068890 | ||||||
chr2:216068904
|
C | CAGATCTC others(7): Show |
1 | a0001c0001t0001g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.125-2400_125-2387d others(16): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068904 | ||||||
chr2:216068953
|
G | A | 4 | a0001c0011t0006g0383a0006c0005t0009g0217a0006c0005t0009g0381others(1): Show | 4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-2435C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068953 | ||||||
chr2:216069069
|
C | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(277): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.125-2551G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069069 | ||||||
chr2:216069139
|
C | T | 14 | a0001c0001t0004g0312a0001c0001t0005g0313a0001c0001t0005g0314others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-2621G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069139 | ||||||
chr2:216069173
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2655C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069173 | ||||||
chr2:216069174
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2656G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069174 | ||||||
chr2:216069175
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2657T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069175 | ||||||
chr2:216069195
|
C | T | 1 | a0001c0001t0005g0386 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-2677G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069195 | ||||||
chr2:216069197
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2679T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069197 | ||||||
chr2:216069199
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2681G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069199 | ||||||
chr2:216069318
|
G | T | 1 | a0001c0001t0001g0006 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.125-2800C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069318 | ||||||
chr2:216069339
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2821G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069339 | ||||||
chr2:216069348
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2830G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069348 | ||||||
chr2:216069359
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2841T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069359 | ||||||
chr2:216069366
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2848T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069366 | ||||||
chr2:216069370
|
A | T | 1 | a0002c0002t0002g0123 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.125-2852T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069370 | ||||||
chr2:216069392
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2874G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069392 | ||||||
chr2:216069397
|
G | A | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-2879C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069397 | ||||||
chr2:216069397
|
G | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(77): Show | 85 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.125-2879C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069397 | ||||||
chr2:216069401
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2883C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069401 | ||||||
chr2:216069403
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2885G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069403 | ||||||
chr2:216069404
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2886A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069404 | ||||||
chr2:216069413
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2895T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069413 | ||||||
chr2:216069453
|
T | G | 2 | a0002c0002t0002g0365a0002c0002t0002g0380 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.125-2935A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069453 | ||||||
chr2:216069474
|
T | A | 2 | a0002c0002t0002g0365a0002c0002t0002g0380 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.125-2956A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069474 | ||||||
chr2:216069514
|
C | T | 2 | a0002c0002t0002g0365a0002c0002t0002g0380 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.125-2996G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069514 | ||||||
chr2:216069574
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.125-3056C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069574 | ||||||
chr2:216069693
|
T | G | 1 | a0006c0005t0009g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125-3175A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069693 | ||||||
chr2:216069706
|
G | C | 3 | a0001c0004t0001g0089a0001c0004t0001g0090a0001c0004t0001g0385 | 3 | HG02145.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.125-3188C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069706 | ||||||
chr2:216069734
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0056a0001c0001t0001g0097others(27): Show | 33 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.125-3216C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069734 | ||||||
chr2:216069765
|
T | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0001g0058others(34): Show | 40 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.125-3247A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069765 | ||||||
chr2:216069808
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(326): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.125-3290G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069808 | ||||||
chr2:216069830
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.125-3312C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069830 | ||||||
chr2:216069900
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.125-3382G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069900 | ||||||
chr2:216069934
|
C | CA | 10 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0078others(7): Show | 10 | HG01175.hp1 NA18943.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-3417dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069934 | ||||||
chr2:216069934
|
CAAA | C | 161 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 165 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.125-3419_125-3417d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069934 | ||||||
chr2:216069934
|
CAAAA | C | 6 | a0001c0001t0001g0181a0001c0001t0004g0373a0001c0001t0004g0374others(3): Show | 7 | HG00544.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-3420_125-3417d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069934 | ||||||
chr2:216069979
|
T | C | 1 | a0002c0002t0002g0240 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.125-3461A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069979 | ||||||
chr2:216070011
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3493C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070011 | ||||||
chr2:216070012
|
A | G | 1 | a0001c0001t0005g0386 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-3494T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070012 | ||||||
chr2:216070012
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3494T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070012 | ||||||
chr2:216070014
|
C | T | 1 | a0002c0002t0002g0101 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.125-3496G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070014 | ||||||
chr2:216070020
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3502T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070020 | ||||||
chr2:216070035
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3517T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070035 | ||||||
chr2:216070038
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3520T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070038 | ||||||
chr2:216070046
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3528T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070046 | ||||||
chr2:216070061
|
T | C | 59 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0001g0082others(56): Show | 61 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-3543A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070061 | ||||||
chr2:216070071
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3553T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070071 | ||||||
chr2:216070073
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3555T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070073 | ||||||
chr2:216070076
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3558T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070076 | ||||||
chr2:216070078
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3560T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070078 | ||||||
chr2:216070079
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3561T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070079 | ||||||
chr2:216070082
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3564A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070082 | ||||||
chr2:216070083
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3565T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070083 | ||||||
chr2:216070088
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3570T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070088 | ||||||
chr2:216070093
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3575T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070093 | ||||||
chr2:216070140
|
AAC | A | 3 | a0001c0001t0006g0023a0001c0003t0003g0241a0007c0008t0002g0321 | 3 | HG02572.hp1 NA19083.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.125-3624_125-3623d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070140 | ||||||
chr2:216070176
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3658A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070176 | ||||||
chr2:216070308
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3790T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070308 | ||||||
chr2:216070308
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.125-3790T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070308 | ||||||
chr2:216070309
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3791G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070309 | ||||||
chr2:216070316
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3798G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070316 | ||||||
chr2:216070323
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3805G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070323 | ||||||
chr2:216070324
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3806T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070324 | ||||||
chr2:216070325
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3807G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070325 | ||||||
chr2:216070327
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3809T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070327 | ||||||
chr2:216070328
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3810A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070328 | ||||||
chr2:216070329
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3811A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070329 | ||||||
chr2:216070331
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3813A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070331 | ||||||
chr2:216070334
|
G | C | 60 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(57): Show | 62 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.125-3816C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070334 | ||||||
chr2:216070335
|
A | T | 60 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(57): Show | 62 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.125-3817T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070335 | ||||||
chr2:216070336
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3818T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070336 | ||||||
chr2:216070343
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3825T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070343 | ||||||
chr2:216070344
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3826T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070344 | ||||||
chr2:216070345
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3827A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070345 | ||||||
chr2:216070347
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3829G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070347 | ||||||
chr2:216070349
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3831G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070349 | ||||||
chr2:216070350
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3832T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070350 | ||||||
chr2:216070361
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3843T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070361 | ||||||
chr2:216070363
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3845G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070363 | ||||||
chr2:216070376
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3858C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070376 | ||||||
chr2:216070377
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3859G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070377 | ||||||
chr2:216070382
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3864G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070382 | ||||||
chr2:216070383
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3865T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070383 | ||||||
chr2:216070386
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3868T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070386 | ||||||
chr2:216070390
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3872G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070390 | ||||||
chr2:216070391
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3873T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070391 | ||||||
chr2:216070393
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3875G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070393 | ||||||
chr2:216070394
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3876T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070394 | ||||||
chr2:216070395
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3877C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070395 | ||||||
chr2:216070396
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3878T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070396 | ||||||
chr2:216070398
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3880G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070398 | ||||||
chr2:216070400
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3882A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070400 | ||||||
chr2:216070458
|
T | A | 29 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(26): Show | 30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.125-3940A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070458 | ||||||
chr2:216070532
|
G | A | 3 | a0001c0003t0003g0094a0001c0003t0003g0095a0001c0003t0003g0234 | 3 | HG00140.hp2 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.125-4014C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070532 | ||||||
chr2:216070585
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.125-4067G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070585 | ||||||
chr2:216070665
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-4147C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070665 | ||||||
chr2:216070700
|
T | C | 29 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(26): Show | 30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.125-4182A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070700 | ||||||
chr2:216070867
|
C | T | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-4349G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070867 | ||||||
chr2:216070876
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.125-4358C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070876 | ||||||
chr2:216070953
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0016others(34): Show | 39 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.125-4435G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070953 | ||||||
chr2:216071252
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-4734C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071252 | ||||||
chr2:216071445
|
C | CA | 4 | a0001c0001t0001g0096a0001c0001t0006g0099a0001c0003t0003g0098others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4928dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071445 | ||||||
chr2:216071449
|
G | A | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(218): Show | 228 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.125-4931C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071449 | ||||||
chr2:216071707
|
G | C | 33 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(30): Show | 34 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-5189C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071707 | ||||||
chr2:216071928
|
A | G | 30 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(27): Show | 31 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.125-5410T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071928 | ||||||
chr2:216071935
|
A | G | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-5417T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071935 | ||||||
chr2:216072036
|
C | T | 1 | a0002c0002t0002g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.125-5518G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072036 | ||||||
chr2:216072130
|
A | C | 4 | a0001c0001t0004g0373a0001c0001t0004g0374a0001c0003t0003g0011others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-5612T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072130 | ||||||
chr2:216072143
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.125-5625G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072143 | ||||||
chr2:216072317
|
C | T | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-5799G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072317 | ||||||
chr2:216072466
|
C | A | 33 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(30): Show | 34 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-5948G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072466 | ||||||
chr2:216072761
|
A | G | 2 | a0002c0002t0002g0380a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.125-6243T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072761 | ||||||
chr2:216073191
|
A | C | 1 | a0001c0001t0001g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.125-6673T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073191 | ||||||
chr2:216073211
|
T | C | 1 | a0001c0001t0005g0386 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-6693A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073211 | ||||||
chr2:216073398
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.125-6880G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073398 | ||||||
chr2:216073760
|
C | T | 1 | a0001c0003t0003g0011 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.125-7242G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073760 | ||||||
chr2:216074270
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.124+7348G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074270 | ||||||
chr2:216074300
|
A | G | 1 | a0004c0009t0001g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124+7318T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074300 | ||||||
chr2:216074345
|
A | G | 1 | a0006c0005t0009g0381 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.124+7273T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074345 | ||||||
chr2:216074441
|
AAAAAGAA others(2): Show |
A | 35 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0349others(32): Show | 36 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.124+7168_124+7176d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074441 | ||||||
chr2:216074466
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7152T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074466 | ||||||
chr2:216074470
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.124+7148T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074470 | ||||||
chr2:216074474
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7144C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074474 | ||||||
chr2:216074478
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124+7140C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074478 | ||||||
chr2:216074480
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7138C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074480 | ||||||
chr2:216074485
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7133T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074485 | ||||||
chr2:216074488
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.124+7130C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074488 | ||||||
chr2:216074489
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7129T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074489 | ||||||
chr2:216074492
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124+7126T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074492 | ||||||
chr2:216074493
|
A | AAAGG | 73 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0035others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.124+7121_124+7124d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
A | AAAGGAAG others(1): Show |
57 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(54): Show | 61 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.124+7117_124+7124d others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
A | AAAGGAAG others(5): Show |
36 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(33): Show | 39 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.124+7113_124+7124d others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
A | AAAGGAAG others(9): Show |
8 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(5): Show | 8 | HG01934.hp1 HG01943.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+7109_124+7124d others(18): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
A | AAAGGAAG others(13): Show |
8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0003t0003g0091others(5): Show | 8 | HG00558.hp2 NA18747.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+7105_124+7124d others(22): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124+7125T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
AAAGG | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0063others(24): Show | 27 | HG00609.hp2 HG00733.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.124+7121_124+7124d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
AAAGGAAG others(1): Show |
A | 17 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0071others(14): Show | 18 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.124+7117_124+7124d others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
AAAGGAAG others(5): Show |
A | 48 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(45): Show | 49 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.124+7113_124+7124d others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
AAAGGAAG others(9): Show |
A | 19 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(16): Show | 19 | HG01884.hp2 HG01975.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.124+7109_124+7124d others(18): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074493
|
AAAGGAAG others(13): Show |
A | 1 | a0001c0001t0005g0386 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124+7105_124+7124d others(22): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | ||||||
chr2:216074497
|
GAAGGAAG others(37): Show |
G | 1 | a0001c0001t0006g0023 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.124+7077_124+7120d others(46): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074497 | ||||||
chr2:216074517
|
G | A | 1 | a0002c0002t0002g0380 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124+7101C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074517 | ||||||
chr2:216074517
|
GAAGGAAG others(17): Show |
G | 29 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(26): Show | 30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.124+7077_124+7100d others(26): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074517 | ||||||
chr2:216074525
|
G | A | 1 | a0002c0002t0002g0380 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124+7093C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074525 | ||||||
chr2:216074529
|
GAAGGAAG others(5): Show |
G | 1 | a0002c0002t0002g0380 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124+7077_124+7088d others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074529 | ||||||
chr2:216074537
|
G | A | 2 | a0002c0002t0002g0220a0002c0002t0002g0222 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.124+7081C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074537 | ||||||
chr2:216074541
|
A | G | 4 | a0002c0002t0002g0110a0002c0002t0002g0220a0002c0002t0002g0222others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+7077T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074541 | ||||||
chr2:216074545
|
G | A | 29 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(26): Show | 30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.124+7073C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074545 | ||||||
chr2:216074634
|
G | T | 10 | a0001c0001t0004g0312a0001c0001t0004g0315a0001c0001t0005g0313others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+6984C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074634 | ||||||
chr2:216074667
|
T | C | 1 | a0001c0003t0003g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.124+6951A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074667 | ||||||
chr2:216074680
|
G | T | 1 | a0001c0003t0003g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.124+6938C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074680 | ||||||
chr2:216074885
|
G | A | 1 | a0008c0015t0001g0258 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.124+6733C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074885 | ||||||
chr2:216075659
|
C | T | 1 | a0001c0003t0003g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.124+5959G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216075659 | ||||||
chr2:216075693
|
T | C | 32 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(29): Show | 33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+5925A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216075693 | ||||||
chr2:216075976
|
C | T | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+5642G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216075976 | ||||||
chr2:216076038
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.124+5580T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076038 | ||||||
chr2:216076209
|
T | C | 1 | a0001c0003t0003g0095 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.124+5409A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076209 | ||||||
chr2:216076274
|
C | A | 32 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(29): Show | 33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+5344G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076274 | ||||||
chr2:216076278
|
C | T | 2 | a0002c0002t0002g0334a0002c0002t0002g0335 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.124+5340G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076278 | ||||||
chr2:216076404
|
G | A | 28 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(25): Show | 29 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.124+5214C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076404 | ||||||
chr2:216076456
|
G | A | 1 | a0007c0008t0002g0321 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.124+5162C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076456 | ||||||
chr2:216076463
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.124+5155T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076463 | ||||||
chr2:216076505
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124+5113A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076505 | ||||||
chr2:216076518
|
T | G | 31 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(28): Show | 32 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.124+5100A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076518 | ||||||
chr2:216076707
|
C | T | 1 | a0002c0002t0002g0108 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.124+4911G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076707 | ||||||
chr2:216076750
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02129.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.124+4868G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076750 | ||||||
chr2:216076751
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02129.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.124+4867A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076751 | ||||||
chr2:216076766
|
C | T | 32 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(29): Show | 33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+4852G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076766 | ||||||
chr2:216077000
|
C | CA | 149 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(146): Show | 154 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.124+4617dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077000 | ||||||
chr2:216077047
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.124+4571C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077047 | ||||||
chr2:216077100
|
T | C | 1 | a0002c0002t0002g0322 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.124+4518A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077100 | ||||||
chr2:216077141
|
G | T | 31 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(28): Show | 32 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.124+4477C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077141 | ||||||
chr2:216077150
|
G | A | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+4468C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077150 | ||||||
chr2:216077322
|
C | T | 4 | a0001c0001t0004g0373a0001c0001t0004g0374a0001c0003t0003g0011others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+4296G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077322 | ||||||
chr2:216077329
|
AC | A | 259 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 268 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.124+4288delG | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077329 | ||||||
chr2:216077398
|
T | A | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+4220A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077398 | ||||||
chr2:216077431
|
C | T | 27 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(24): Show | 28 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.124+4187G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077431 | ||||||
chr2:216077432
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.124+4186C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077432 | ||||||
chr2:216077529
|
C | T | 10 | a0001c0001t0004g0312a0001c0001t0004g0315a0001c0001t0005g0313others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+4089G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077529 | ||||||
chr2:216077715
|
A | G | 32 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(29): Show | 33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+3903T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077715 | ||||||
chr2:216077723
|
C | T | 1 | a0001c0001t0005g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124+3895G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077723 | ||||||
chr2:216077794
|
A | G | 1 | a0001c0004t0001g0385 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+3824T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077794 | ||||||
chr2:216077806
|
C | CA | 20 | a0001c0001t0001g0017a0001c0001t0001g0076a0001c0001t0001g0077others(17): Show | 20 | HG01106.hp2 HG01175.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.124+3811dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077806 | ||||||
chr2:216077806
|
CA | C | 112 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(109): Show | 116 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.124+3811delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077806 | ||||||
chr2:216077806
|
CAA | C | 11 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0333others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+3810_124+3811d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077806 | ||||||
chr2:216077927
|
G | A | 10 | a0001c0001t0004g0312a0001c0001t0004g0315a0001c0001t0005g0313others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+3691C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077927 | ||||||
chr2:216078020
|
T | TA | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0109others(110): Show | 117 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.124+3597dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078020 | ||||||
chr2:216078167
|
G | A | 7 | a0002c0002t0002g0365a0002c0002t0002g0366a0002c0002t0002g0367others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+3451C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078167 | ||||||
chr2:216078200
|
G | C | 2 | a0002c0002t0002g0380a0006c0005t0009g0381 | 2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124+3418C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078200 | ||||||
chr2:216078309
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.124+3309C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078309 | ||||||
chr2:216078419
|
T | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0102others(88): Show | 94 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+3199A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078419 | ||||||
chr2:216078552
|
T | C | 51 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(48): Show | 52 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.124+3066A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078552 | ||||||
chr2:216078567
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 42 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.124+3051C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078567 | ||||||
chr2:216078568
|
A | C | 4 | a0001c0004t0001g0089a0001c0004t0001g0090a0005c0007t0001g0021others(1): Show | 4 | HG02145.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+3050T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078568 | ||||||
chr2:216078577
|
A | G | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 146 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.124+3041T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078577 | ||||||
chr2:216078683
|
T | C | 3 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG00609.hp1 HG00673.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.124+2935A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078683 | ||||||
chr2:216078721
|
T | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0082a0001c0001t0001g0083others(11): Show | 15 | HG01975.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.124+2897A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078721 | ||||||
chr2:216078998
|
T | G | 1 | a0001c0004t0001g0385 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+2620A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078998 | ||||||
chr2:216079151
|
C | CT | 36 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0349others(33): Show | 36 | HG00140.hp2 HG01099.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.124+2466dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079151 | ||||||
chr2:216079151
|
CT | C | 17 | a0001c0001t0001g0346a0001c0001t0004g0312a0001c0001t0004g0315others(14): Show | 17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.124+2466delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079151 | ||||||
chr2:216079179
|
T | G | 1 | a0002c0002t0002g0322 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.124+2439A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079179 | ||||||
chr2:216079182
|
A | AT | 13 | a0001c0001t0001g0349a0001c0001t0004g0350a0001c0001t0004g0351others(10): Show | 13 | HG01975.hp2 HG02056.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+2435dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079182 | ||||||
chr2:216079490
|
C | A | 31 | a0001c0001t0001g0323a0001c0001t0001g0329a0001c0001t0001g0330others(28): Show | 33 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+2128G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079490 | ||||||
chr2:216079517
|
G | A | 1 | a0001c0003t0003g0348 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.124+2101C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079517 | ||||||
chr2:216079583
|
A | G | 1 | a0001c0004t0001g0385 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+2035T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079583 | ||||||
chr2:216079657
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 5 | NA18954.hp2 NA18975.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+1961C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079657 | ||||||
chr2:216079662
|
C | T | 4 | a0001c0001t0001g0377a0002c0002t0002g0376a0002c0002t0002g0378others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1956G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079662 | ||||||
chr2:216079747
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124+1871G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079747 | ||||||
chr2:216079756
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.124+1862G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079756 | ||||||
chr2:216079757
|
G | A | 29 | a0001c0001t0001g0349a0001c0001t0001g0360a0001c0001t0001g0361others(26): Show | 29 | HG01884.hp1 HG01884.hp2 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.124+1861C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079757 | ||||||
chr2:216079797
|
C | T | 1 | a0002c0002t0002g0376 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.124+1821G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079797 | ||||||
chr2:216079863
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 79 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.124+1755G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079863 | ||||||
chr2:216079955
|
T | C | 1 | a0002c0002t0002g0371 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.124+1663A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079955 | ||||||
chr2:216079981
|
C | CA | 5 | a0001c0001t0001g0372a0001c0001t0004g0373a0001c0001t0004g0374others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+1636dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079981 | ||||||
chr2:216080113
|
G | A | 1 | a0001c0001t0001g0375 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.124+1505C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080113 | ||||||
chr2:216080133
|
G | A | 7 | a0001c0001t0001g0377a0001c0001t0005g0386a0002c0002t0002g0376others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+1485C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080133 | ||||||
chr2:216080230
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.124+1388G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080230 | ||||||
chr2:216080706
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG00738.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.124+912C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080706 | ||||||
chr2:216080962
|
C | G | 1 | a0002c0002t0002g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.124+656G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080962 | ||||||
chr2:216080980
|
A | C | 2 | a0001c0004t0001g0385a0001c0011t0006g0383 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.124+638T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080980 | ||||||
chr2:216081106
|
T | C | 1 | a0001c0001t0001g0382 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.124+512A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081106 | ||||||
chr2:216081137
|
T | G | 1 | a0001c0011t0006g0383 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+481A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081137 | ||||||
chr2:216081226
|
G | A | 1 | a0001c0001t0001g0384 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.124+392C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081226 | ||||||
chr2:216081230
|
GACTC | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+384_124+387del others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081230 | ||||||
chr2:216081326
|
T | A | 2 | a0001c0001t0005g0386a0001c0004t0001g0385 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.124+292A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081326 |