geneid | 26577 |
---|---|
ensemblid | ENSG00000163710.9 |
hgncid | 8739 |
symbol | PCOLCE2 |
name | procollagen C-endopeptidase enhancer 2 |
refseq_nuc | NM_013363.4 |
refseq_prot | NP_037495.1 |
ensembl_nuc | ENST00000295992.8 |
ensembl_prot | ENSP00000295992.3 |
mane_status | MANE Select |
chr | chr3 |
start | 142817874 |
end | 142889083 |
strand | - |
ver | v1.2 |
region | chr3:142817874-142889083 |
region5000 | chr3:142812874-142894083 |
regionname0 | PCOLCE2_chr3_142817874_142889083 |
regionname5000 | PCOLCE2_chr3_142812874_142894083 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 415 | 311 | 83 | 56 | 121 | 12 | 37 | 85 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002 | 0/0 | 415 | 18 | 3 | 4 | 10 | 1 | 0 | 6 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0003 | 0/0 | 415 | 10 | 0 | 6 | 0 | 3 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0004 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0005 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0006 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1248 | 306 | 79 | 55 | 121 | 12 | 37 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0002 | 0/0 | 1248 | 18 | 3 | 4 | 10 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0003 | 0/0 | 1248 | 10 | 0 | 6 | 0 | 3 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0004 | 0/0 | 1248 | 4 | 4 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0005 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0006 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0007 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
c0008 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 649 | 175 | 53 | 32 | 59 | 8 | 21 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0002 | 0/0 | 649 | 71 | 21 | 6 | 40 | 2 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0003 | 0/0 | 671 | 38 | 7 | 15 | 6 | 4 | 6 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0004 | 0/0 | 649 | 28 | 0 | 5 | 21 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0005 | 0/0 | 671 | 11 | 2 | 5 | 0 | 2 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0006 | 0/0 | 649 | 10 | 0 | 2 | 3 | 0 | 5 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0007 | 0/0 | 649 | 3 | 3 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0008 | 0/0 | 649 | 3 | 0 | 0 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0009 | 0/0 | 671 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0010 | 0/0 | 649 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
t0011 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0017 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1248 | 306 | 79 | 55 | 121 | 12 | 37 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0004 | 0/0 | 1248 | 4 | 4 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0007 | 0/0 | 1248 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002c0002 | 0/0 | 1248 | 18 | 3 | 4 | 10 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0003c0003 | 0/0 | 1248 | 10 | 0 | 6 | 0 | 3 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0004c0005 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0005c0008 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0006c0006 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1896 | 160 | 48 | 27 | 55 | 8 | 20 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0002 | 0/0 | 1896 | 64 | 19 | 6 | 36 | 1 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0003 | 0/0 | 1918 | 33 | 7 | 13 | 6 | 1 | 6 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0004 | 0/0 | 1896 | 23 | 0 | 3 | 18 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0005 | 0/0 | 1918 | 9 | 2 | 3 | 0 | 2 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0006 | 0/0 | 1896 | 10 | 0 | 2 | 3 | 0 | 5 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0007 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0008 | 0/0 | 1896 | 3 | 0 | 0 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0009 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0010 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0001t0011 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0004t0001 | 0/0 | 1896 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0004t0002 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0004t0007 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0001c0007t0001 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002c0002t0001 | 0/0 | 1896 | 4 | 1 | 0 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002c0002t0002 | 0/0 | 1896 | 6 | 1 | 0 | 4 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002c0002t0004 | 0/0 | 1896 | 5 | 0 | 2 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002c0002t0005 | 0/0 | 1918 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0002c0002t0007 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0003c0003t0001 | 0/0 | 1896 | 5 | 0 | 4 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0003c0003t0003 | 0/0 | 1918 | 5 | 0 | 2 | 0 | 3 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0004c0005t0001 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0005c0008t0001 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
a0006c0006t0001 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | copy fasta | chr3 | 142812874 | 142894083 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0017 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0010g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0001t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0004t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0004t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0001c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0002c0002t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0004c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0005c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
a0006c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | GBR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0197 | EUR | GBR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0051 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00544 | hp2 | a0002 | c0002 | t0004 | g0100 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00738 | hp2 | a0003 | c0003 | t0003 | g0035 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01070 | hp1 | a0002 | c0002 | t0005 | g0041 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01074 | hp1 | a0003 | c0003 | t0003 | g0053 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0080 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0307 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01256 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01258 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01346 | hp2 | a0002 | c0002 | t0005 | g0039 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0135 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01496 | hp2 | a0001 | c0007 | t0001 | g0218 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01516 | hp1 | a0003 | c0003 | t0003 | g0054 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0064 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0322 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0082 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0066 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02922 | hp2 | a0001 | c0004 | t0007 | g0321 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02976 | hp1 | a0004 | c0005 | t0001 | g0244 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0078 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03486 | hp1 | a0002 | c0002 | t0007 | g0139 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0101 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03579 | hp1 | a0001 | c0004 | t0002 | g0320 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0285 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0067 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0077 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18944 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18946 | hp1 | a0005 | c0008 | t0001 | g0212 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18949 | hp1 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18950 | hp2 | a0002 | c0002 | t0004 | g0099 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18960 | hp1 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18980 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18984 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19055 | hp2 | a0001 | c0001 | t0008 | g0315 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19058 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0142 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ASW | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ASW | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0049 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20752 | hp2 | a0003 | c0003 | t0003 | g0063 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0062 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20805 | hp2 | a0003 | c0003 | t0003 | g0050 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02109 | hp2 | a0006 | c0006 | t0001 | g0147 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0323 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0287 | REF | REF | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142820985
|
G | A | 1 | a0005 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1010C>T | p.Ser337Leu | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/9 | 1197/1896 | 1010/1248 | 337/415 | chr3 | 142820985 | ||
chr3:142823607
|
G | T | 1 | a0003 | 10 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(7): Show |
missense_variant | MODERATE | c.874C>A | p.Pro292Thr | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/9 | 1061/1896 | 874/1248 | 292/415 | chr3 | 142823607 | ||
chr3:142829718
|
A | G | 2 | a0002a0004 | 19 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(16): Show |
missense_variant | MODERATE | c.839T>C | p.Val280Ala | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/9 | 1026/1896 | 839/1248 | 280/415 | chr3 | 142829718 | ||
chr3:142838825
|
C | T | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.655G>A | p.Gly219Arg | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/9 | 842/1896 | 655/1248 | 219/415 | chr3 | 142838825 | ||
chr3:142848403
|
A | G | 1 | a0004 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.262T>C | p.Tyr88His | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/9 | 449/1896 | 262/1248 | 88/415 | chr3 | 142848403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142820939
|
C | T | 1 | a0001c0007 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1056G>A | p.Ala352Ala | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/9 | 1243/1896 | 1056/1248 | 352/415 | chr3 | 142820939 | ||
chr3:142888893
|
T | G | 1 | a0001c0004 | 4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.4A>C | p.Arg2Arg | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 191/1896 | 4/1248 | 2/415 | chr3 | 142888893 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142818066
|
C | T | 1 | a0001c0001t0010 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 269 | chr3 | 142818066 | |||||
chr3:142818175
|
G | A | 4 | a0001c0001t0007a0001c0001t0009a0001c0004t0007others(1): Show | 4 | HG02922.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 160 | chr3 | 142818175 | |||||
chr3:142818196
|
T | G | 1 | a0001c0001t0008 | 3 | NA18949.hp1 NA18984.hp2 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 139 | chr3 | 142818196 | |||||
chr3:142818229
|
C | G | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(8): Show | 114 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*106G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 106 | chr3 | 142818229 | |||||
chr3:142888903
|
G | T | 1 | a0001c0001t0011 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 7 | chr3 | 142888903 | |||||
chr3:142888925
|
C | T | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(1): Show | 39 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-29G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 29 | chr3 | 142888925 | |||||
chr3:142888980
|
C | CGCTCACA others(15): Show |
5 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(2): Show | 50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-106_-85dupCAGCGCT others(15): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 85 | chr3 | 142888980 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:142818531
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0006g0082 | 2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1118-66C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818531 | ||||||
chr3:142818684
|
G | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0136others(29): Show | 33 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1118-219C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818684 | ||||||
chr3:142818712
|
C | G | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1118-247G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818712 | ||||||
chr3:142818828
|
C | T | 3 | a0001c0001t0002g0009a0001c0001t0002g0196a0001c0001t0002g0248 | 4 | NA18971.hp2 NA18972.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1118-363G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818828 | ||||||
chr3:142818839
|
G | A | 8 | a0001c0001t0001g0173a0001c0001t0001g0251a0001c0001t0001g0252others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1118-374C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818839 | ||||||
chr3:142818897
|
C | T | 10 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0116others(7): Show | 10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1118-432G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818897 | ||||||
chr3:142818916
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1118-451C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818916 | ||||||
chr3:142818924
|
G | A | 19 | a0001c0001t0002g0201a0001c0001t0002g0207a0001c0001t0002g0253others(16): Show | 20 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.1118-459C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818924 | ||||||
chr3:142818964
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1118-499A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818964 | ||||||
chr3:142818965
|
G | C | 17 | a0001c0001t0002g0009a0001c0001t0002g0106a0001c0001t0002g0107others(14): Show | 18 | HG01884.hp1 HG02027.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1118-500C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818965 | ||||||
chr3:142819165
|
G | A | 10 | a0001c0001t0002g0013a0001c0001t0002g0140a0001c0001t0002g0144others(7): Show | 11 | HG02280.hp1 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1118-700C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819165 | ||||||
chr3:142819275
|
T | C | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1118-810A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819275 | ||||||
chr3:142819426
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1118-961C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819426 | ||||||
chr3:142819497
|
A | T | 2 | a0001c0001t0001g0311a0001c0004t0001g0322 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1118-1032T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819497 | ||||||
chr3:142819554
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1118-1089C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819554 | ||||||
chr3:142819733
|
C | A | 10 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0116others(7): Show | 10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+1145G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819733 | ||||||
chr3:142819807
|
G | A | 54 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(51): Show | 58 | HG00280.hp2 HG00597.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1117+1071C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819807 | ||||||
chr3:142819962
|
T | TTC | 10 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0116others(7): Show | 10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+914_1117+915d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819962 | ||||||
chr3:142819980
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1117+898C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819980 | ||||||
chr3:142820107
|
A | AT | 12 | a0001c0001t0001g0159a0001c0001t0002g0013a0001c0001t0002g0140others(9): Show | 13 | HG02280.hp1 HG02451.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.1117+770dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820107 | ||||||
chr3:142820107
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0241a0001c0001t0003g0038others(1): Show | 5 | HG00280.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+771T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820107 | ||||||
chr3:142820107
|
AT | A | 26 | a0001c0001t0002g0124a0001c0001t0002g0146a0001c0001t0002g0149others(23): Show | 27 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1117+770delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820107 | ||||||
chr3:142820121
|
T | A | 5 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0318others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+757A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820121 | ||||||
chr3:142820160
|
C | A | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1117+718G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820160 | ||||||
chr3:142820295
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1117+583G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820295 | ||||||
chr3:142820530
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1117+348G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820530 | ||||||
chr3:142820647
|
C | T | 10 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0116others(7): Show | 10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+231G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820647 | ||||||
chr3:142820687
|
A | C | 11 | a0001c0001t0002g0120a0001c0001t0002g0231a0001c0001t0004g0071others(8): Show | 11 | HG00423.hp2 HG01934.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1117+191T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820687 | ||||||
chr3:142820783
|
G | A | 1 | a0002c0002t0002g0302 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1117+95C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820783 | ||||||
chr3:142821137
|
A | G | 1 | a0001c0001t0003g0047 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.950-92T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821137 | ||||||
chr3:142821290
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.950-245C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821290 | ||||||
chr3:142821311
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.950-266G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821311 | ||||||
chr3:142821340
|
CTTGA | C | 3 | a0001c0001t0001g0136a0001c0001t0002g0146a0001c0001t0002g0264 | 3 | HG02615.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.950-299_950-296del others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821340 | ||||||
chr3:142821351
|
C | T | 22 | a0001c0001t0001g0136a0001c0001t0002g0009a0001c0001t0002g0106others(19): Show | 23 | HG01884.hp1 HG02027.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.950-306G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821351 | ||||||
chr3:142821441
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.950-396C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821441 | ||||||
chr3:142821581
|
G | C | 45 | a0001c0001t0001g0117a0001c0001t0001g0136a0001c0001t0001g0143others(42): Show | 46 | HG00642.hp1 HG00735.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.950-536C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821581 | ||||||
chr3:142821609
|
T | C | 4 | a0001c0001t0002g0270a0002c0002t0004g0098a0002c0002t0004g0099others(1): Show | 4 | HG00544.hp2 NA18950.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-564A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821609 | ||||||
chr3:142821693
|
C | CT | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-649dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821693 | ||||||
chr3:142821693
|
CT | C | 78 | a0001c0001t0001g0220a0001c0001t0002g0014a0001c0001t0002g0018others(75): Show | 83 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.950-649delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821693 | ||||||
chr3:142821781
|
G | A | 23 | a0001c0001t0001g0136a0001c0001t0001g0235a0001c0001t0002g0009others(20): Show | 24 | HG00735.hp1 HG01884.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.950-736C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821781 | ||||||
chr3:142821792
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.950-747G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821792 | ||||||
chr3:142821858
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.950-813C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821858 | ||||||
chr3:142821888
|
G | C | 1 | a0001c0001t0002g0014 | 2 | NA18953.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.950-843C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821888 | ||||||
chr3:142821913
|
T | G | 25 | a0001c0001t0001g0136a0001c0001t0001g0235a0001c0001t0002g0009others(22): Show | 26 | HG00735.hp1 HG01884.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.950-868A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821913 | ||||||
chr3:142821916
|
G | T | 39 | a0001c0001t0002g0018a0001c0001t0002g0120a0001c0001t0002g0156others(36): Show | 41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.950-871C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821916 | ||||||
chr3:142821973
|
A | T | 1 | a0001c0001t0005g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.950-928T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821973 | ||||||
chr3:142822031
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.950-986G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822031 | ||||||
chr3:142822066
|
C | T | 9 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(6): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.950-1021G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822066 | ||||||
chr3:142822074
|
C | A | 1 | a0001c0001t0003g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.950-1029G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822074 | ||||||
chr3:142822122
|
T | G | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-1077A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822122 | ||||||
chr3:142822241
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0246a0001c0001t0003g0024others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.950-1196G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822241 | ||||||
chr3:142822299
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.949+1233T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822299 | ||||||
chr3:142822672
|
A | C | 20 | a0001c0001t0002g0201a0001c0001t0002g0207a0001c0001t0002g0253others(17): Show | 22 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.949+860T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822672 | ||||||
chr3:142822769
|
G | A | 1 | a0001c0001t0010g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.949+763C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822769 | ||||||
chr3:142822778
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.949+754T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822778 | ||||||
chr3:142822845
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(124): Show | 134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.949+687A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822845 | ||||||
chr3:142823046
|
A | C | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+486T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823046 | ||||||
chr3:142823159
|
C | T | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+373G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823159 | ||||||
chr3:142823192
|
T | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(140): Show | 151 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.949+340A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823192 | ||||||
chr3:142823402
|
C | A | 4 | a0001c0001t0005g0002a0001c0001t0005g0032a0001c0001t0005g0049others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.949+130G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823402 | ||||||
chr3:142823439
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.949+93G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823439 | ||||||
chr3:142823644
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.866-29C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823644 | ||||||
chr3:142823823
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.866-208A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823823 | ||||||
chr3:142823841
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(124): Show | 134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-226A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823841 | ||||||
chr3:142823899
|
A | G | 86 | a0001c0001t0001g0173a0001c0001t0001g0220a0001c0001t0001g0251others(83): Show | 91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.866-284T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823899 | ||||||
chr3:142823914
|
C | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0036 | 3 | HG01346.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.866-299G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823914 | ||||||
chr3:142823981
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-366A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823981 | ||||||
chr3:142824089
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0159a0001c0001t0001g0162others(3): Show | 6 | NA18946.hp1 NA18947.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.866-474A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824089 | ||||||
chr3:142824125
|
C | T | 2 | a0001c0001t0002g0124a0001c0001t0002g0254 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.866-510G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824125 | ||||||
chr3:142824176
|
AACTAAGA others(60): Show |
A | 4 | a0001c0001t0001g0125a0001c0001t0006g0089a0002c0002t0001g0169others(1): Show | 4 | NA18980.hp2 NA19070.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-628_866-562del others(67): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824176 | ||||||
chr3:142824250
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0002g0219a0001c0001t0002g0250 | 3 | NA18985.hp1 NA19012.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.866-635G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824250 | ||||||
chr3:142824264
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.866-649A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824264 | ||||||
chr3:142824411
|
G | C | 3 | a0001c0001t0007g0187a0001c0001t0009g0027a0001c0004t0007g0321 | 3 | HG02922.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.866-796C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824411 | ||||||
chr3:142824432
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0001g0308 | 3 | HG02129.hp2 NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.866-817C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824432 | ||||||
chr3:142824457
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.866-842G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824457 | ||||||
chr3:142824491
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0006g0078 | 2 | HG03017.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.866-876A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824491 | ||||||
chr3:142824598
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.866-983A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824598 | ||||||
chr3:142824621
|
C | CTGTTAAT others(6): Show |
10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1019_866-1007d others(15): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824621 | ||||||
chr3:142824664
|
G | A | 84 | a0001c0001t0001g0173a0001c0001t0001g0220a0001c0001t0001g0251others(81): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.866-1049C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824664 | ||||||
chr3:142824671
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.866-1056C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824671 | ||||||
chr3:142824679
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0157others(4): Show | 7 | HG02015.hp1 HG02165.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.866-1064C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824679 | ||||||
chr3:142824726
|
A | G | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1111T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824726 | ||||||
chr3:142824782
|
G | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.866-1167C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824782 | ||||||
chr3:142824809
|
G | A | 9 | a0001c0001t0001g0126a0001c0001t0001g0154a0001c0001t0001g0178others(6): Show | 9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.866-1194C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824809 | ||||||
chr3:142824816
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(124): Show | 134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-1201A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824816 | ||||||
chr3:142824886
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(124): Show | 133 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.866-1271A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824886 | ||||||
chr3:142824930
|
T | G | 87 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0180others(84): Show | 91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.866-1315A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824930 | ||||||
chr3:142824991
|
A | T | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.866-1376T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824991 | ||||||
chr3:142825051
|
A | T | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1436T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825051 | ||||||
chr3:142825091
|
A | T | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1476T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825091 | ||||||
chr3:142825201
|
G | A | 30 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0116others(27): Show | 31 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.866-1586C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825201 | ||||||
chr3:142825295
|
C | T | 1 | a0002c0002t0004g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.866-1680G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825295 | ||||||
chr3:142825401
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0154a0001c0001t0001g0233others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-1786C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825401 | ||||||
chr3:142825422
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1807C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825422 | ||||||
chr3:142825564
|
A | C | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1949T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825564 | ||||||
chr3:142826005
|
C | CT | 11 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(8): Show | 12 | HG00423.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.866-2391dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826005 | ||||||
chr3:142826124
|
C | T | 1 | a0001c0001t0006g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.866-2509G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826124 | ||||||
chr3:142826166
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0277a0001c0001t0006g0086 | 3 | NA18944.hp2 NA18953.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.866-2551C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826166 | ||||||
chr3:142826224
|
G | A | 1 | a0001c0001t0003g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.866-2609C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826224 | ||||||
chr3:142826229
|
G | A | 2 | a0001c0001t0005g0029a0001c0001t0005g0040 | 2 | HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.866-2614C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826229 | ||||||
chr3:142826244
|
T | G | 1 | a0001c0001t0004g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.866-2629A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826244 | ||||||
chr3:142826250
|
A | G | 128 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(125): Show | 134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-2635T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826250 | ||||||
chr3:142826272
|
T | G | 128 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0137others(125): Show | 134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-2657A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826272 | ||||||
chr3:142826307
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.866-2692C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826307 | ||||||
chr3:142826596
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-2981A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826596 | ||||||
chr3:142826656
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 9 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.865+3036G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826656 | ||||||
chr3:142826661
|
C | T | 2 | a0001c0001t0001g0311a0001c0004t0001g0322 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.865+3031G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826661 | ||||||
chr3:142826729
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+2963G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826729 | ||||||
chr3:142826802
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.865+2890G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826802 | ||||||
chr3:142826805
|
T | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0104others(27): Show | 32 | HG00438.hp1 HG00639.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.865+2887A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826805 | ||||||
chr3:142827036
|
T | C | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+2656A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827036 | ||||||
chr3:142827092
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0264 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.865+2600T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827092 | ||||||
chr3:142827149
|
G | A | 5 | a0001c0001t0002g0009a0001c0001t0002g0124a0001c0001t0002g0196others(2): Show | 6 | HG02970.hp1 NA18971.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+2543C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827149 | ||||||
chr3:142827179
|
C | G | 10 | a0001c0001t0001g0226a0001c0001t0002g0013a0001c0001t0002g0140others(7): Show | 11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+2513G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827179 | ||||||
chr3:142827211
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0154a0001c0001t0001g0233others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+2481G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827211 | ||||||
chr3:142827212
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0003g0048 | 2 | HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.865+2480C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827212 | ||||||
chr3:142827512
|
C | T | 139 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0118others(136): Show | 146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.865+2180G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827512 | ||||||
chr3:142827532
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.865+2160G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827532 | ||||||
chr3:142827538
|
T | TAC | 4 | a0001c0001t0001g0226a0001c0001t0007g0187a0001c0001t0009g0027others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+2152_865+2153d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827538 | ||||||
chr3:142827599
|
G | A | 5 | a0001c0001t0001g0136a0001c0001t0001g0226a0001c0001t0007g0187others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+2093C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827599 | ||||||
chr3:142827634
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.865+2058G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827634 | ||||||
chr3:142827901
|
G | T | 32 | a0001c0001t0001g0123a0001c0001t0001g0176a0001c0001t0001g0177others(29): Show | 33 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.865+1791C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827901 | ||||||
chr3:142828041
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.865+1651G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828041 | ||||||
chr3:142828043
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.865+1649G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828043 | ||||||
chr3:142828274
|
G | A | 1 | a0001c0001t0004g0091 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.865+1418C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828274 | ||||||
chr3:142828378
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0199 | 2 | NA19055.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.865+1314T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828378 | ||||||
chr3:142828420
|
T | C | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(39): Show | 47 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.865+1272A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828420 | ||||||
chr3:142828552
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.865+1140C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828552 | ||||||
chr3:142828575
|
C | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(153): Show | 167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.865+1117G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828575 | ||||||
chr3:142828588
|
G | A | 1 | a0001c0001t0003g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.865+1104C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828588 | ||||||
chr3:142828645
|
C | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+1047G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828645 | ||||||
chr3:142828720
|
G | A | 10 | a0001c0001t0001g0143a0001c0001t0001g0174a0001c0001t0001g0175others(7): Show | 10 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.865+972C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828720 | ||||||
chr3:142828828
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+864A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828828 | ||||||
chr3:142828834
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+858C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828834 | ||||||
chr3:142828911
|
T | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(43): Show | 51 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.865+781A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828911 | ||||||
chr3:142828957
|
A | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+735T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828957 | ||||||
chr3:142829110
|
C | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+582G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829110 | ||||||
chr3:142829113
|
C | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.865+579G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829113 | ||||||
chr3:142829161
|
C | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+531G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829161 | ||||||
chr3:142829193
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.865+499G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829193 | ||||||
chr3:142829227
|
AAAAT | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(110): Show | 121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.865+461_865+464del others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829227 | ||||||
chr3:142829281
|
C | CA | 35 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0117others(32): Show | 37 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.865+410dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829281 | ||||||
chr3:142829512
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(112): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.865+180G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829512 | ||||||
chr3:142829622
|
TTTC | T | 7 | a0001c0001t0001g0182a0001c0001t0001g0235a0001c0001t0001g0249others(4): Show | 7 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.865+67_865+69delGA others(1): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829622 | ||||||
chr3:142829899
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.711-53A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142829899 | ||||||
chr3:142830633
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.711-787A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142830633 | ||||||
chr3:142830707
|
C | T | 1 | a0004c0005t0001g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.711-861G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142830707 | ||||||
chr3:142831023
|
G | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0002g0106others(3): Show | 6 | HG00597.hp1 HG02027.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-1177C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831023 | ||||||
chr3:142831042
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.711-1196C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831042 | ||||||
chr3:142831243
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.711-1397A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831243 | ||||||
chr3:142831306
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.711-1460C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831306 | ||||||
chr3:142831513
|
G | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0235a0001c0001t0001g0311others(2): Show | 5 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-1667C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831513 | ||||||
chr3:142831674
|
A | C | 1 | a0002c0002t0002g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.711-1828T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831674 | ||||||
chr3:142832095
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.711-2249T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832095 | ||||||
chr3:142832140
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.711-2294G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832140 | ||||||
chr3:142832229
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.711-2383C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832229 | ||||||
chr3:142832256
|
T | C | 1 | a0003c0003t0003g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.711-2410A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832256 | ||||||
chr3:142832296
|
T | G | 4 | a0001c0001t0001g0182a0001c0001t0001g0311a0001c0001t0005g0055others(1): Show | 4 | HG01175.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-2450A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832296 | ||||||
chr3:142832342
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0003g0003a0001c0001t0003g0036others(1): Show | 5 | HG01346.hp1 HG02080.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-2496G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832342 | ||||||
chr3:142832414
|
G | A | 23 | a0001c0001t0002g0140a0001c0001t0002g0151a0001c0001t0002g0167others(20): Show | 24 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.711-2568C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832414 | ||||||
chr3:142832514
|
C | T | 2 | a0002c0002t0001g0152a0002c0002t0002g0142 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.711-2668G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832514 | ||||||
chr3:142832549
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.711-2703T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832549 | ||||||
chr3:142832681
|
G | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0235a0001c0001t0001g0311others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-2835C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832681 | ||||||
chr3:142832722
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.711-2876G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832722 | ||||||
chr3:142832753
|
CA | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.711-2908delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832753 | ||||||
chr3:142832955
|
A | C | 1 | a0001c0001t0002g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.711-3109T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832955 | ||||||
chr3:142833008
|
A | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(47): Show | 53 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.711-3162T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833008 | ||||||
chr3:142833095
|
C | G | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.711-3249G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833095 | ||||||
chr3:142833159
|
G | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0249 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.711-3313C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833159 | ||||||
chr3:142833182
|
T | C | 50 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(47): Show | 53 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.711-3336A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833182 | ||||||
chr3:142833384
|
A | G | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(111): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.711-3538T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833384 | ||||||
chr3:142833481
|
CT | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(42): Show | 49 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.711-3636delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833481 | ||||||
chr3:142833790
|
G | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(86): Show | 96 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.711-3944C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833790 | ||||||
chr3:142833816
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.711-3970A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833816 | ||||||
chr3:142834161
|
C | T | 1 | a0002c0002t0004g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.711-4315G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834161 | ||||||
chr3:142834166
|
T | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.711-4320A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834166 | ||||||
chr3:142834247
|
C | A | 2 | a0001c0001t0008g0315a0001c0001t0008g0316 | 2 | NA18949.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.711-4401G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834247 | ||||||
chr3:142834253
|
C | T | 1 | a0002c0002t0004g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.711-4407G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834253 | ||||||
chr3:142834336
|
G | T | 1 | a0001c0001t0004g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.710+4434C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834336 | ||||||
chr3:142834471
|
T | C | 1 | a0003c0003t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.710+4299A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834471 | ||||||
chr3:142834594
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.710+4176T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834594 | ||||||
chr3:142834828
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0002g0146 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.710+3942A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834828 | ||||||
chr3:142834830
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.710+3940C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834830 | ||||||
chr3:142835004
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710+3766G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835004 | ||||||
chr3:142835012
|
T | C | 1 | a0001c0001t0001g0287 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.710+3758A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835012 | ||||||
chr3:142835159
|
T | G | 2 | a0001c0001t0004g0075a0001c0001t0004g0076 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.710+3611A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835159 | ||||||
chr3:142835194
|
T | G | 15 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0213others(12): Show | 16 | HG00597.hp1 HG02027.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.710+3576A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835194 | ||||||
chr3:142835238
|
T | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0249 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.710+3532A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835238 | ||||||
chr3:142835308
|
T | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+3462A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835308 | ||||||
chr3:142835311
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.710+3459T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835311 | ||||||
chr3:142835333
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(31): Show | 37 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.710+3437A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835333 | ||||||
chr3:142835516
|
A | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(86): Show | 96 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.710+3254T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835516 | ||||||
chr3:142835517
|
A | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(108): Show | 120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.710+3253T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835517 | ||||||
chr3:142835614
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(85): Show | 95 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.710+3156T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835614 | ||||||
chr3:142835627
|
T | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(73): Show | 83 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.710+3143A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835627 | ||||||
chr3:142835732
|
T | C | 1 | a0001c0001t0008g0316 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.710+3038A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835732 | ||||||
chr3:142835815
|
T | A | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(108): Show | 120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.710+2955A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835815 | ||||||
chr3:142835893
|
C | A | 6 | a0002c0002t0001g0111a0002c0002t0001g0169a0002c0002t0001g0170others(3): Show | 6 | HG00544.hp2 NA18950.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+2877G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835893 | ||||||
chr3:142835893
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.710+2877G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835893 | ||||||
chr3:142836001
|
A | AT | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(72): Show | 82 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.710+2768dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836001 | ||||||
chr3:142836121
|
T | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0249 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.710+2649A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836121 | ||||||
chr3:142836133
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.710+2637C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836133 | ||||||
chr3:142836151
|
C | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(72): Show | 82 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.710+2619G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836151 | ||||||
chr3:142836175
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(85): Show | 95 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.710+2595G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836175 | ||||||
chr3:142836329
|
T | G | 1 | a0001c0001t0003g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.710+2441A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836329 | ||||||
chr3:142836386
|
G | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(72): Show | 82 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.710+2384C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836386 | ||||||
chr3:142836504
|
G | A | 1 | a0001c0001t0001g0008 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.710+2266C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836504 | ||||||
chr3:142836573
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.710+2197A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836573 | ||||||
chr3:142836578
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0011g0101 | 2 | HG00735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.710+2192A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836578 | ||||||
chr3:142836649
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.710+2121A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836649 | ||||||
chr3:142836699
|
G | A | 9 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0178others(6): Show | 9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.710+2071C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836699 | ||||||
chr3:142837004
|
A | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1766T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837004 | ||||||
chr3:142837006
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.710+1764C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837006 | ||||||
chr3:142837099
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.710+1671G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837099 | ||||||
chr3:142837364
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0002g0146 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.710+1406C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837364 | ||||||
chr3:142837453
|
C | CTTAATA | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(85): Show | 95 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.710+1316_710+1317i others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837453 | ||||||
chr3:142837513
|
C | T | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1257G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837513 | ||||||
chr3:142837557
|
A | G | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1213T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837557 | ||||||
chr3:142837576
|
GA | G | 6 | a0001c0001t0002g0245a0001c0001t0002g0309a0001c0001t0004g0083others(3): Show | 6 | HG00597.hp2 HG02135.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.710+1193delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837576 | ||||||
chr3:142837741
|
T | C | 1 | a0001c0001t0002g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.710+1029A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837741 | ||||||
chr3:142837748
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1022C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837748 | ||||||
chr3:142838247
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.710+523T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142838247 | ||||||
chr3:142838392
|
T | G | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.710+378A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142838392 | ||||||
chr3:142838565
|
T | C | 4 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0184others(1): Show | 4 | HG00673.hp1 HG02132.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+205A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142838565 | ||||||
chr3:142839002
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-96G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839002 | ||||||
chr3:142839064
|
T | TA | 6 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0243others(3): Show | 7 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-159dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839064 | ||||||
chr3:142839312
|
T | C | 3 | a0001c0001t0008g0203a0001c0001t0008g0315a0001c0001t0008g0316 | 3 | NA18949.hp1 NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.574-406A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839312 | ||||||
chr3:142839315
|
AT | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0182others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-410delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839315 | ||||||
chr3:142839464
|
C | T | 3 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0074 | 3 | NA18747.hp1 NA18989.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.574-558G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839464 | ||||||
chr3:142839501
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0235a0001c0001t0001g0311others(1): Show | 4 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-595G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839501 | ||||||
chr3:142839742
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.574-836A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839742 | ||||||
chr3:142839867
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.574-961A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839867 | ||||||
chr3:142839973
|
G | T | 1 | a0001c0001t0004g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.574-1067C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839973 | ||||||
chr3:142840195
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(37): Show | 44 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.574-1289G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840195 | ||||||
chr3:142840319
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0006g0082 | 2 | HG02735.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.574-1413T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840319 | ||||||
chr3:142840379
|
C | T | 62 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(59): Show | 68 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.574-1473G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840379 | ||||||
chr3:142840689
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0003g0003a0001c0001t0003g0036others(1): Show | 5 | HG01346.hp1 HG02080.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1783A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840689 | ||||||
chr3:142840691
|
T | C | 1 | a0001c0001t0004g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.574-1785A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840691 | ||||||
chr3:142840762
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0002g0255 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.574-1856G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840762 | ||||||
chr3:142840846
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0002g0144a0001c0001t0002g0239others(2): Show | 5 | HG02451.hp1 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1940G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840846 | ||||||
chr3:142840944
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573+1980C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840944 | ||||||
chr3:142841024
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573+1900C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841024 | ||||||
chr3:142841029
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0210a0001c0001t0006g0084 | 3 | HG01257.hp1 HG01952.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.573+1895G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841029 | ||||||
chr3:142841074
|
C | CA | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(81): Show | 92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.573+1849dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841074 | ||||||
chr3:142841125
|
A | T | 2 | a0001c0001t0001g0136a0001c0001t0002g0146 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.573+1799T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841125 | ||||||
chr3:142841210
|
G | A | 72 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(69): Show | 79 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.573+1714C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841210 | ||||||
chr3:142841225
|
C | A | 8 | a0002c0002t0001g0111a0002c0002t0001g0169a0002c0002t0001g0170others(5): Show | 8 | HG00544.hp2 HG02056.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+1699G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841225 | ||||||
chr3:142841335
|
A | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(39): Show | 46 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+1589T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841335 | ||||||
chr3:142841523
|
G | C | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.573+1401C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841523 | ||||||
chr3:142841551
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.573+1373A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841551 | ||||||
chr3:142841555
|
ATTACT | A | 4 | a0001c0001t0002g0151a0001c0001t0002g0167a0001c0001t0002g0264others(1): Show | 4 | HG00738.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+1364_573+1368d others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841555 | ||||||
chr3:142842000
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.573+924T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842000 | ||||||
chr3:142842037
|
A | C | 2 | a0001c0001t0001g0136a0001c0001t0002g0146 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.573+887T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842037 | ||||||
chr3:142842103
|
C | G | 1 | a0001c0001t0002g0312 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.573+821G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842103 | ||||||
chr3:142842149
|
G | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.573+775C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842149 | ||||||
chr3:142842285
|
T | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.573+639A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842285 | ||||||
chr3:142842353
|
A | G | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(91): Show | 102 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.573+571T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842353 | ||||||
chr3:142842517
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.573+407G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842517 | ||||||
chr3:142842654
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(39): Show | 46 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+270C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842654 | ||||||
chr3:142842739
|
C | CA | 7 | a0001c0001t0001g0136a0001c0001t0001g0182a0001c0001t0001g0235others(4): Show | 7 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+184dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842739 | ||||||
chr3:142842739
|
C | CAA | 22 | a0001c0001t0001g0005a0001c0001t0002g0140a0001c0001t0002g0151others(19): Show | 24 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.573+183_573+184dup others(2): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842739 | ||||||
chr3:142842760
|
G | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573+164C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842760 | ||||||
chr3:142842791
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.573+133T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842791 | ||||||
chr3:142843111
|
G | A | 2 | a0001c0001t0003g0034a0003c0003t0001g0135 | 2 | HG01361.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.449-63C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843111 | ||||||
chr3:142843291
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.449-243G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843291 | ||||||
chr3:142843312
|
T | C | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-264A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843312 | ||||||
chr3:142843646
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.449-598T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843646 | ||||||
chr3:142843841
|
C | A | 2 | a0001c0001t0003g0034a0003c0003t0001g0135 | 2 | HG01361.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.449-793G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843841 | ||||||
chr3:142843879
|
T | C | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.449-831A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843879 | ||||||
chr3:142843968
|
T | G | 1 | a0001c0001t0004g0090 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.449-920A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843968 | ||||||
chr3:142844205
|
A | G | 1 | a0001c0001t0011g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.449-1157T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844205 | ||||||
chr3:142844265
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-1217G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844265 | ||||||
chr3:142844335
|
T | C | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.449-1287A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844335 | ||||||
chr3:142844395
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.449-1347A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844395 | ||||||
chr3:142844452
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.449-1404C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844452 | ||||||
chr3:142844472
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0122a0001c0001t0001g0272others(3): Show | 7 | HG01884.hp2 HG02735.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1424A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844472 | ||||||
chr3:142844631
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.449-1583G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844631 | ||||||
chr3:142844958
|
AGAC | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0003g0056 | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1913_449-1911d others(5): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844958 | ||||||
chr3:142844966
|
T | C | 41 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.449-1918A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844966 | ||||||
chr3:142845164
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.449-2116C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845164 | ||||||
chr3:142845482
|
T | C | 52 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(49): Show | 56 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.449-2434A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845482 | ||||||
chr3:142845578
|
T | G | 1 | a0001c0001t0003g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.449-2530A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845578 | ||||||
chr3:142845619
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.449-2571G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845619 | ||||||
chr3:142845739
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.448+2478G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845739 | ||||||
chr3:142845755
|
A | G | 25 | a0001c0001t0001g0141a0001c0001t0001g0154a0001c0001t0001g0171others(22): Show | 26 | HG00642.hp1 HG00735.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+2462T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845755 | ||||||
chr3:142845762
|
G | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0136a0001c0001t0001g0226others(4): Show | 7 | HG02258.hp1 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+2455C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845762 | ||||||
chr3:142845778
|
C | T | 3 | a0001c0001t0002g0155a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG01891.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.448+2439G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845778 | ||||||
chr3:142845804
|
G | A | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0189others(5): Show | 8 | HG02015.hp1 HG02165.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+2413C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845804 | ||||||
chr3:142845866
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2351A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845866 | ||||||
chr3:142845867
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2350A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845867 | ||||||
chr3:142845868
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2349C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845868 | ||||||
chr3:142845870
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2347C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845870 | ||||||
chr3:142845874
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2343A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845874 | ||||||
chr3:142845875
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2342A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845875 | ||||||
chr3:142845876
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2341C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845876 | ||||||
chr3:142845877
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2340T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845877 | ||||||
chr3:142845952
|
T | G | 2 | a0001c0001t0002g0232a0001c0004t0001g0322 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.448+2265A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845952 | ||||||
chr3:142846011
|
G | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0118a0001c0001t0001g0143others(61): Show | 69 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.448+2206C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846011 | ||||||
chr3:142846060
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.448+2157A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846060 | ||||||
chr3:142846230
|
G | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0311 | 3 | HG01175.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+1987C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846230 | ||||||
chr3:142846257
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0311 | 3 | HG01175.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+1960C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846257 | ||||||
chr3:142846286
|
C | T | 7 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0182others(4): Show | 7 | HG01175.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.448+1931G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846286 | ||||||
chr3:142846288
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.448+1929A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846288 | ||||||
chr3:142846313
|
T | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0182a0001c0001t0001g0311others(2): Show | 5 | HG01175.hp2 HG02559.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+1904A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846313 | ||||||
chr3:142846678
|
T | G | 1 | a0001c0001t0002g0293 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.448+1539A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846678 | ||||||
chr3:142846723
|
T | C | 93 | a0001c0001t0001g0119a0001c0001t0001g0143a0001c0001t0001g0159others(90): Show | 97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.448+1494A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846723 | ||||||
chr3:142846728
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.448+1489G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846728 | ||||||
chr3:142846778
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.448+1439A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846778 | ||||||
chr3:142846952
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+1265G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846952 | ||||||
chr3:142846996
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.448+1221G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846996 | ||||||
chr3:142847482
|
T | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0206a0001c0001t0001g0289others(2): Show | 5 | HG00438.hp2 HG02083.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+735A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847482 | ||||||
chr3:142847495
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0119others(107): Show | 117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.448+722C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847495 | ||||||
chr3:142847533
|
G | GTA | 2 | a0001c0001t0002g0018a0001c0001t0002g0303 | 3 | HG02056.hp2 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.448+682_448+683dup others(2): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847533 | ||||||
chr3:142847541
|
A | G | 1 | a0002c0002t0005g0041 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.448+676T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847541 | ||||||
chr3:142847750
|
TG | T | 39 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(36): Show | 40 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.448+466delC | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847750 | ||||||
chr3:142847762
|
T | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.448+455A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847762 | ||||||
chr3:142847834
|
G | C | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.448+383C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847834 | ||||||
chr3:142847989
|
T | C | 1 | a0001c0001t0005g0032 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.448+228A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847989 | ||||||
chr3:142847999
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.448+218G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847999 | ||||||
chr3:142848004
|
T | C | 4 | a0001c0001t0001g0171a0001c0001t0001g0243a0001c0001t0001g0261others(1): Show | 4 | HG00738.hp1 HG02895.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+213A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142848004 | ||||||
chr3:142848132
|
A | T | 1 | a0001c0001t0002g0106 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.448+85T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142848132 | ||||||
chr3:142848188
|
T | C | 34 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(31): Show | 35 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.448+29A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142848188 | ||||||
chr3:142848485
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(172): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.193-13C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848485 | ||||||
chr3:142848589
|
C | G | 2 | a0001c0001t0001g0154a0001c0001t0002g0155 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.193-117G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848589 | ||||||
chr3:142848687
|
G | T | 3 | a0002c0002t0001g0152a0002c0002t0002g0142a0002c0002t0007g0139 | 3 | HG02922.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-215C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848687 | ||||||
chr3:142848741
|
G | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-269C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848741 | ||||||
chr3:142848760
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-288C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848760 | ||||||
chr3:142848803
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0145others(26): Show | 32 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.193-331G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848803 | ||||||
chr3:142848882
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-410T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848882 | ||||||
chr3:142848920
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.193-448C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848920 | ||||||
chr3:142849069
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-597G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849069 | ||||||
chr3:142849078
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193-606C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849078 | ||||||
chr3:142849084
|
C | T | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-612G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849084 | ||||||
chr3:142849091
|
T | C | 5 | a0001c0001t0002g0312a0001c0001t0004g0079a0001c0001t0008g0203others(2): Show | 5 | NA18949.hp1 NA18984.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-619A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849091 | ||||||
chr3:142849101
|
C | T | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-629G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849101 | ||||||
chr3:142849139
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0297a0001c0001t0002g0116 | 3 | NA19012.hp2 NA19074.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.193-667G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849139 | ||||||
chr3:142849152
|
CA | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(172): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.193-681delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849152 | ||||||
chr3:142849262
|
A | C | 1 | a0002c0002t0002g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.193-790T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849262 | ||||||
chr3:142849306
|
T | A | 2 | a0001c0001t0002g0151a0001c0001t0005g0055 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.193-834A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849306 | ||||||
chr3:142849314
|
C | G | 1 | a0001c0001t0002g0116 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.193-842G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849314 | ||||||
chr3:142849320
|
T | C | 7 | a0001c0001t0001g0143a0001c0001t0001g0178a0001c0001t0001g0208others(4): Show | 7 | HG01496.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-848A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849320 | ||||||
chr3:142849551
|
G | A | 1 | a0002c0002t0007g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.193-1079C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849551 | ||||||
chr3:142849886
|
C | T | 7 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0251others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-1414G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849886 | ||||||
chr3:142849950
|
T | A | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193-1478A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849950 | ||||||
chr3:142850105
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-1633T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850105 | ||||||
chr3:142850151
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-1679T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850151 | ||||||
chr3:142850172
|
GTTT | G | 37 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(34): Show | 38 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.193-1703_193-1701d others(5): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850172 | ||||||
chr3:142850179
|
G | C | 1 | a0001c0001t0002g0291 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.193-1707C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850179 | ||||||
chr3:142850305
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-1833G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850305 | ||||||
chr3:142850414
|
G | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0208a0001c0001t0001g0229 | 3 | HG02886.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.193-1942C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850414 | ||||||
chr3:142850534
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.193-2062C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850534 | ||||||
chr3:142850758
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-2286T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850758 | ||||||
chr3:142850808
|
G | T | 1 | a0001c0001t0010g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193-2336C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850808 | ||||||
chr3:142850812
|
A | ACT | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(173): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-2341_193-2340i others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850812 | ||||||
chr3:142850875
|
T | G | 3 | a0001c0001t0001g0173a0001c0001t0002g0262a0006c0006t0001g0147 | 3 | HG02109.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.193-2403A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850875 | ||||||
chr3:142850964
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0267others(3): Show | 7 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2492C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850964 | ||||||
chr3:142851023
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.193-2551T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851023 | ||||||
chr3:142851060
|
T | C | 1 | a0001c0001t0002g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.193-2588A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851060 | ||||||
chr3:142851092
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.193-2620A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851092 | ||||||
chr3:142851122
|
G | C | 1 | a0001c0001t0002g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.193-2650C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851122 | ||||||
chr3:142851201
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0002g0140others(1): Show | 5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-2729A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851201 | ||||||
chr3:142851541
|
A | T | 8 | a0001c0001t0001g0171a0001c0001t0001g0179a0001c0001t0001g0180others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.193-3069T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851541 | ||||||
chr3:142851578
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.193-3106T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851578 | ||||||
chr3:142851596
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0263 | 2 | HG00323.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.193-3124C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851596 | ||||||
chr3:142851619
|
G | T | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-3147C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851619 | ||||||
chr3:142851749
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0156 | 2 | HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.193-3277G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851749 | ||||||
chr3:142851989
|
G | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02280.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-3517C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851989 | ||||||
chr3:142852112
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0002g0254 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-3640A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852112 | ||||||
chr3:142852222
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193-3750T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852222 | ||||||
chr3:142852245
|
A | G | 44 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(41): Show | 45 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-3773T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852245 | ||||||
chr3:142852276
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-3804G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852276 | ||||||
chr3:142852355
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-3883C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852355 | ||||||
chr3:142852421
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.193-3949A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852421 | ||||||
chr3:142852533
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-4061T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852533 | ||||||
chr3:142852647
|
A | ATG | 11 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0190others(8): Show | 12 | HG01891.hp1 HG02074.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.193-4177_193-4176d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | ||||||
chr3:142852647
|
A | ATGTG | 6 | a0001c0001t0001g0117a0001c0001t0001g0175a0001c0001t0002g0149others(3): Show | 6 | HG02055.hp2 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-4179_193-4176d others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | ||||||
chr3:142852647
|
A | ATGTGTG | 3 | a0001c0001t0001g0154a0001c0001t0001g0266a0001c0001t0002g0155 | 3 | HG01891.hp2 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.193-4181_193-4176d others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | ||||||
chr3:142852647
|
ATG | A | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(42): Show | 53 | HG00639.hp2 HG00673.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.193-4177_193-4176d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | ||||||
chr3:142852647
|
ATGTG | A | 5 | a0001c0001t0001g0267a0001c0001t0002g0254a0001c0001t0002g0275others(2): Show | 5 | HG02132.hp1 HG02630.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-4179_193-4176d others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | ||||||
chr3:142852717
|
A | G | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4245T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852717 | ||||||
chr3:142852725
|
T | G | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4253A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852725 | ||||||
chr3:142852787
|
T | C | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-4315A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852787 | ||||||
chr3:142852791
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.193-4319G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852791 | ||||||
chr3:142852844
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.193-4372G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852844 | ||||||
chr3:142852932
|
G | A | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4460C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852932 | ||||||
chr3:142853101
|
T | TA | 36 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0117others(33): Show | 37 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.193-4630dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853101 | ||||||
chr3:142853101
|
TA | T | 8 | a0001c0001t0001g0176a0001c0001t0001g0199a0001c0001t0001g0215others(5): Show | 8 | HG01496.hp1 HG01993.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-4630delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853101 | ||||||
chr3:142853139
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-4667G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853139 | ||||||
chr3:142853214
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-4742A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853214 | ||||||
chr3:142853334
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193-4862G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853334 | ||||||
chr3:142853422
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.193-4950A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853422 | ||||||
chr3:142853456
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0002g0254 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-4984A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853456 | ||||||
chr3:142853624
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-5152T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853624 | ||||||
chr3:142853745
|
C | T | 6 | a0001c0001t0002g0231a0001c0001t0004g0085a0001c0001t0004g0087others(3): Show | 6 | HG00423.hp2 NA18960.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-5273G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853745 | ||||||
chr3:142853752
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193-5280A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853752 | ||||||
chr3:142853773
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0002g0124 | 2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.193-5301G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853773 | ||||||
chr3:142854078
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(164): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.193-5606G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854078 | ||||||
chr3:142854166
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.193-5694G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854166 | ||||||
chr3:142854208
|
C | CAT | 181 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(178): Show | 190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.193-5737_193-5736i others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854208 | ||||||
chr3:142854209
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.193-5737C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854209 | ||||||
chr3:142854262
|
A | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0156 | 2 | HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.193-5790T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854262 | ||||||
chr3:142854321
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(164): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.193-5849G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854321 | ||||||
chr3:142854329
|
AGTTGATC others(18): Show |
A | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-5882_193-5858d others(27): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854329 | ||||||
chr3:142854486
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.193-6014T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854486 | ||||||
chr3:142854532
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.193-6060A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854532 | ||||||
chr3:142854613
|
C | A | 44 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(41): Show | 45 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-6141G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854613 | ||||||
chr3:142854651
|
G | A | 44 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(41): Show | 45 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-6179C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854651 | ||||||
chr3:142854688
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(112): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-6216G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854688 | ||||||
chr3:142854695
|
G | A | 7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-6223C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854695 | ||||||
chr3:142854947
|
T | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(112): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-6475A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854947 | ||||||
chr3:142855019
|
G | T | 1 | a0001c0001t0001g0300 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.193-6547C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855019 | ||||||
chr3:142855033
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-6561C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855033 | ||||||
chr3:142855281
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-6809C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855281 | ||||||
chr3:142855325
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(112): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-6853G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855325 | ||||||
chr3:142855326
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-6854C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855326 | ||||||
chr3:142855340
|
T | TA | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(165): Show | 177 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-6869dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855340 | ||||||
chr3:142855345
|
T | A | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-6873A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855345 | ||||||
chr3:142855353
|
C | T | 5 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0210others(2): Show | 5 | HG01192.hp2 HG01257.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-6881G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855353 | ||||||
chr3:142855354
|
A | G | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(156): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.193-6882T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855354 | ||||||
chr3:142855439
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193-6967C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855439 | ||||||
chr3:142855463
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-6991C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855463 | ||||||
chr3:142855614
|
G | A | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(156): Show | 168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.193-7142C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855614 | ||||||
chr3:142855705
|
A | C | 163 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(160): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.193-7233T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855705 | ||||||
chr3:142855727
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0002g0156 | 2 | HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.193-7255G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855727 | ||||||
chr3:142855787
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(112): Show | 123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-7315T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855787 | ||||||
chr3:142856086
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0002g0195a0001c0001t0003g0033 | 3 | HG01884.hp1 HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.193-7614G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856086 | ||||||
chr3:142856200
|
C | T | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-7728G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856200 | ||||||
chr3:142856203
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-7731A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856203 | ||||||
chr3:142856371
|
T | C | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-7899A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856371 | ||||||
chr3:142856718
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-8246C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856718 | ||||||
chr3:142856758
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.193-8286G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856758 | ||||||
chr3:142856840
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193-8368T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856840 | ||||||
chr3:142856892
|
CT | C | 50 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(47): Show | 50 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.193-8421delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856892 | ||||||
chr3:142856992
|
C | T | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-8520G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856992 | ||||||
chr3:142857048
|
CTCTATAG others(3): Show |
C | 3 | a0001c0001t0001g0175a0001c0001t0002g0149a0001c0001t0002g0255 | 3 | HG03041.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.193-8586_193-8577d others(12): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857048 | ||||||
chr3:142857053
|
T | C | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-8581A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857053 | ||||||
chr3:142857054
|
A | G | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-8582T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857054 | ||||||
chr3:142857059
|
G | C | 3 | a0001c0001t0001g0175a0001c0001t0002g0149a0001c0001t0002g0255 | 3 | HG03041.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.193-8587C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857059 | ||||||
chr3:142857166
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-8694G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857166 | ||||||
chr3:142857412
|
C | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-8940G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857412 | ||||||
chr3:142857440
|
T | C | 2 | a0002c0002t0002g0142a0002c0002t0007g0139 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-8968A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857440 | ||||||
chr3:142857593
|
A | G | 4 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0005g0049others(1): Show | 4 | HG01261.hp2 HG03490.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-9121T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857593 | ||||||
chr3:142857613
|
C | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-9141G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857613 | ||||||
chr3:142857637
|
G | A | 4 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0025others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-9165C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857637 | ||||||
chr3:142857689
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193-9217G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857689 | ||||||
chr3:142857706
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.193-9234A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857706 | ||||||
chr3:142857875
|
C | T | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.193-9403G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857875 | ||||||
chr3:142857905
|
C | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-9433G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857905 | ||||||
chr3:142857912
|
A | C | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(166): Show | 178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-9440T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857912 | ||||||
chr3:142857958
|
C | A | 1 | a0001c0001t0001g0318 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193-9486G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857958 | ||||||
chr3:142858539
|
T | C | 1 | a0001c0001t0003g0021 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193-10067A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858539 | ||||||
chr3:142858657
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193-10185A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858657 | ||||||
chr3:142858735
|
A | ATG | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0117others(107): Show | 117 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.193-10265_193-1026 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858735 | ||||||
chr3:142858735
|
A | ATGTG | 3 | a0001c0001t0001g0267a0001c0001t0002g0254a0002c0002t0004g0098 | 3 | HG02630.hp1 NA18960.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-10267_193-1026 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858735 | ||||||
chr3:142858735
|
A | G | 1 | a0001c0001t0002g0317 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.193-10263T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858735 | ||||||
chr3:142858750
|
T | TGC | 29 | a0001c0001t0001g0143a0001c0001t0001g0166a0001c0001t0001g0178others(26): Show | 31 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.193-10279_193-1027 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858750 | ||||||
chr3:142858780
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-10308C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858780 | ||||||
chr3:142858870
|
C | T | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-10398G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858870 | ||||||
chr3:142858939
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0161a0001c0001t0001g0217 | 4 | HG00673.hp2 NA18942.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-10467G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858939 | ||||||
chr3:142859014
|
C | T | 14 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.193-10542G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859014 | ||||||
chr3:142859069
|
T | C | 1 | a0001c0001t0004g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.193-10597A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859069 | ||||||
chr3:142859078
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.193-10606A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859078 | ||||||
chr3:142859101
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0267a0001c0001t0002g0254 | 3 | HG00642.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-10629G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859101 | ||||||
chr3:142859102
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(24): Show | 31 | HG00438.hp1 HG00673.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-10630C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859102 | ||||||
chr3:142859116
|
G | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0119others(110): Show | 121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.193-10644C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859116 | ||||||
chr3:142859252
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0263a0002c0002t0002g0142others(1): Show | 4 | HG02615.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-10780C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859252 | ||||||
chr3:142859466
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.193-10994A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859466 | ||||||
chr3:142859564
|
G | GT | 6 | a0001c0001t0001g0263a0001c0001t0002g0265a0001c0001t0003g0023others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-11093dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859564 | ||||||
chr3:142859714
|
C | T | 33 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(30): Show | 33 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.193-11242G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859714 | ||||||
chr3:142859778
|
G | A | 3 | a0001c0001t0001g0141a0002c0002t0002g0142a0002c0002t0007g0139 | 3 | HG02615.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-11306C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859778 | ||||||
chr3:142859850
|
A | G | 9 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-11378T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859850 | ||||||
chr3:142859855
|
T | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-11383A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859855 | ||||||
chr3:142859944
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-11472A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859944 | ||||||
chr3:142859962
|
A | G | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(115): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.193-11490T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859962 | ||||||
chr3:142860055
|
T | TA | 9 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-11584dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860055 | ||||||
chr3:142860111
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.193-11639T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860111 | ||||||
chr3:142860149
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193-11677C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860149 | ||||||
chr3:142860370
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.193-11898A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860370 | ||||||
chr3:142860388
|
A | T | 182 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(179): Show | 191 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.193-11916T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860388 | ||||||
chr3:142860403
|
T | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-11931A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860403 | ||||||
chr3:142860425
|
T | TTTG | 5 | a0001c0001t0001g0226a0001c0001t0001g0263a0001c0001t0002g0013others(2): Show | 6 | HG00642.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-11956_193-1195 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860425 | ||||||
chr3:142860425
|
TTTG | T | 15 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(12): Show | 15 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.193-11956_193-1195 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860425 | ||||||
chr3:142860494
|
T | C | 310 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 328 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.193-12022A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860494 | ||||||
chr3:142860554
|
G | A | 4 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0025others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-12082C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860554 | ||||||
chr3:142860560
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0295 | 2 | HG00438.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.193-12088G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860560 | ||||||
chr3:142860565
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-12093G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860565 | ||||||
chr3:142860669
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193-12197T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860669 | ||||||
chr3:142861102
|
C | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(114): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.193-12630G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861102 | ||||||
chr3:142861242
|
G | C | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0117others(134): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.193-12770C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861242 | ||||||
chr3:142861480
|
T | TATCTTCC | 17 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(14): Show | 17 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-13009_193-1300 others(11): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861480 | ||||||
chr3:142861541
|
CTTG | C | 9 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0175others(6): Show | 9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-13072_193-1307 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861541 | ||||||
chr3:142861615
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.193-13143G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861615 | ||||||
chr3:142861626
|
A | C | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-13154T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861626 | ||||||
chr3:142861655
|
CT | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0118others(118): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.193-13184delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861655 | ||||||
chr3:142862055
|
G | A | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-13583C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862055 | ||||||
chr3:142862123
|
G | A | 56 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(53): Show | 56 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.193-13651C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862123 | ||||||
chr3:142862471
|
T | G | 55 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(52): Show | 55 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.193-13999A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862471 | ||||||
chr3:142862494
|
A | G | 3 | a0001c0001t0001g0141a0002c0002t0002g0142a0002c0002t0007g0139 | 3 | HG02615.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-14022T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862494 | ||||||
chr3:142862500
|
T | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0145others(18): Show | 24 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-14028A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862500 | ||||||
chr3:142862580
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0255 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.193-14108G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862580 | ||||||
chr3:142862651
|
G | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0145others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-14179C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862651 | ||||||
chr3:142862757
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.193-14285C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862757 | ||||||
chr3:142862772
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.193-14300T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862772 | ||||||
chr3:142862948
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-14476C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862948 | ||||||
chr3:142863000
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | NA18944.hp1 NA18961.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-14528C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863000 | ||||||
chr3:142863055
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-14583A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863055 | ||||||
chr3:142863060
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0002g0253 | 3 | HG01433.hp2 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.193-14588G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863060 | ||||||
chr3:142863096
|
CA | C | 221 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(218): Show | 235 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.193-14625delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863096 | ||||||
chr3:142863096
|
CAA | C | 20 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(17): Show | 20 | HG00438.hp2 HG01884.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.193-14626_193-1462 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863096 | ||||||
chr3:142863096
|
CAAA | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0114others(49): Show | 55 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.193-14627_193-1462 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863096 | ||||||
chr3:142863211
|
T | TA | 4 | a0001c0001t0001g0209a0001c0001t0001g0246a0001c0001t0003g0024others(1): Show | 4 | HG01069.hp2 HG01168.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-14740dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863211 | ||||||
chr3:142863252
|
G | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0210a0001c0001t0002g0183others(2): Show | 5 | HG01192.hp2 HG01257.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-14780C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863252 | ||||||
chr3:142863535
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193-15063G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863535 | ||||||
chr3:142863537
|
T | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0311a0001c0001t0002g0156 | 3 | HG01175.hp2 HG04115.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.193-15065A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863537 | ||||||
chr3:142863584
|
T | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0252others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.193-15112A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863584 | ||||||
chr3:142863688
|
G | A | 2 | a0001c0001t0002g0193a0001c0001t0002g0232 | 2 | HG01433.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.193-15216C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863688 | ||||||
chr3:142863797
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(87): Show | 94 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.193-15325A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863797 | ||||||
chr3:142863888
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-15416T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863888 | ||||||
chr3:142863984
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.193-15512G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863984 | ||||||
chr3:142863985
|
G | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0114others(65): Show | 71 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.193-15513C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863985 | ||||||
chr3:142863999
|
G | GA | 67 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0114others(64): Show | 70 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.193-15528dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863999 | ||||||
chr3:142864057
|
G | A | 1 | a0001c0001t0004g0092 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.193-15585C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864057 | ||||||
chr3:142864147
|
A | G | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-15675T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864147 | ||||||
chr3:142864336
|
TGA | T | 7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-15866_193-1586 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864336 | ||||||
chr3:142864406
|
C | A | 1 | a0001c0001t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.193-15934G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864406 | ||||||
chr3:142864407
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.193-15935T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864407 | ||||||
chr3:142864582
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.193-16110C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864582 | ||||||
chr3:142864938
|
T | C | 1 | a0001c0001t0006g0093 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.193-16466A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864938 | ||||||
chr3:142865145
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-16673G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865145 | ||||||
chr3:142865210
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-16738C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865210 | ||||||
chr3:142865319
|
G | GT | 9 | a0001c0001t0001g0006a0001c0001t0001g0171a0001c0001t0001g0233others(6): Show | 10 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-16848dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865319 | ||||||
chr3:142865365
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-16893G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865365 | ||||||
chr3:142865367
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.193-16895C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865367 | ||||||
chr3:142865452
|
AGAGT | A | 11 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0252others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-16984_193-1698 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865452 | ||||||
chr3:142865747
|
T | C | 10 | a0001c0001t0001g0104a0001c0001t0001g0158a0001c0001t0001g0190others(7): Show | 10 | HG00673.hp1 HG02132.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-17275A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865747 | ||||||
chr3:142865778
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-17306C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865778 | ||||||
chr3:142866107
|
T | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0288a0001c0001t0001g0296 | 3 | HG00280.hp1 HG01069.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.193-17635A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866107 | ||||||
chr3:142866206
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-17734C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866206 | ||||||
chr3:142866399
|
T | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-17927A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866399 | ||||||
chr3:142866467
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.193-17995T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866467 | ||||||
chr3:142866515
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-18043T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866515 | ||||||
chr3:142866662
|
T | C | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-18190A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866662 | ||||||
chr3:142866690
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0003g0060a0001c0001t0003g0061 | 3 | HG02559.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.193-18218T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866690 | ||||||
chr3:142866850
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-18378A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866850 | ||||||
chr3:142866854
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-18382G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866854 | ||||||
chr3:142866874
|
T | C | 1 | a0005c0008t0001g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.193-18402A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866874 | ||||||
chr3:142866896
|
C | T | 7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-18424G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866896 | ||||||
chr3:142866946
|
T | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-18474A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866946 | ||||||
chr3:142866948
|
T | C | 29 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(26): Show | 29 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.193-18476A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866948 | ||||||
chr3:142866960
|
T | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(80): Show | 87 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.193-18488A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866960 | ||||||
chr3:142867219
|
T | C | 4 | a0001c0001t0001g0105a0001c0001t0001g0305a0001c0001t0002g0196others(1): Show | 4 | HG00544.hp1 HG02074.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-18747A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867219 | ||||||
chr3:142867292
|
T | C | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-18820A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867292 | ||||||
chr3:142867299
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.193-18827G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867299 | ||||||
chr3:142867327
|
C | T | 1 | a0003c0003t0003g0053 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.193-18855G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867327 | ||||||
chr3:142867343
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-18871G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867343 | ||||||
chr3:142867434
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.193-18962T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867434 | ||||||
chr3:142867476
|
T | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0290a0001c0001t0002g0291 | 3 | HG00323.hp2 HG01496.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.193-19004A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867476 | ||||||
chr3:142867508
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0150a0001c0001t0001g0171others(2): Show | 6 | HG00738.hp1 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-19036G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867508 | ||||||
chr3:142867628
|
C | A | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-19156G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867628 | ||||||
chr3:142867636
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0002g0009a0001c0001t0002g0248 | 4 | NA18972.hp2 NA18973.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-19164C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867636 | ||||||
chr3:142867653
|
CACA | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-19184_193-1918 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867653 | ||||||
chr3:142867714
|
T | G | 2 | a0001c0001t0005g0049a0003c0003t0003g0050 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.193-19242A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867714 | ||||||
chr3:142867909
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(16): Show | 22 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-19437G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867909 | ||||||
chr3:142867955
|
T | C | 1 | a0001c0007t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.193-19483A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867955 | ||||||
chr3:142868019
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-19547G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868019 | ||||||
chr3:142868145
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+19524G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868145 | ||||||
chr3:142868202
|
G | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+19467C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868202 | ||||||
chr3:142868217
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+19452G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868217 | ||||||
chr3:142868484
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+19185T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868484 | ||||||
chr3:142868497
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.192+19172C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868497 | ||||||
chr3:142868661
|
G | A | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192+19008C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868661 | ||||||
chr3:142868731
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+18938G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868731 | ||||||
chr3:142868735
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192+18934G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868735 | ||||||
chr3:142868790
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+18879C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868790 | ||||||
chr3:142868978
|
G | A | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+18691C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868978 | ||||||
chr3:142869019
|
C | T | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+18650G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869019 | ||||||
chr3:142869030
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.192+18639C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869030 | ||||||
chr3:142869108
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.192+18561C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869108 | ||||||
chr3:142869183
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+18486G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869183 | ||||||
chr3:142869184
|
G | A | 28 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(25): Show | 28 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+18485C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869184 | ||||||
chr3:142869207
|
T | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+18462A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869207 | ||||||
chr3:142869216
|
G | A | 3 | a0001c0001t0001g0141a0002c0002t0002g0142a0002c0002t0007g0139 | 3 | HG02615.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+18453C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869216 | ||||||
chr3:142869239
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0001g0308 | 2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.192+18430G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869239 | ||||||
chr3:142869245
|
C | T | 1 | a0002c0002t0005g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.192+18424G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869245 | ||||||
chr3:142869302
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0172 | 3 | HG01515.hp1 HG01517.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.192+18367G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869302 | ||||||
chr3:142869382
|
G | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(37): Show | 43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+18287C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869382 | ||||||
chr3:142869419
|
C | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+18250G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869419 | ||||||
chr3:142869525
|
G | T | 4 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0025others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+18144C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869525 | ||||||
chr3:142869564
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0279a0001c0001t0001g0313others(1): Show | 5 | HG00639.hp2 HG01081.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+18105G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869564 | ||||||
chr3:142869625
|
G | T | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+18044C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869625 | ||||||
chr3:142869932
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+17737T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869932 | ||||||
chr3:142870131
|
A | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+17538T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870131 | ||||||
chr3:142870171
|
C | T | 3 | a0002c0002t0004g0004a0002c0002t0005g0039a0002c0002t0005g0041 | 4 | HG01070.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+17498G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870171 | ||||||
chr3:142870299
|
T | C | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+17370A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870299 | ||||||
chr3:142870310
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.192+17359G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870310 | ||||||
chr3:142870483
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.192+17186A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870483 | ||||||
chr3:142870489
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+17180C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870489 | ||||||
chr3:142870492
|
A | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+17177T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870492 | ||||||
chr3:142870598
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0006g0084 | 2 | HG01952.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.192+17071A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870598 | ||||||
chr3:142870706
|
A | AT | 23 | a0001c0001t0001g0006a0001c0001t0001g0129a0001c0001t0001g0131others(20): Show | 24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.192+16962dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | ||||||
chr3:142870706
|
A | ATT | 41 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0114others(38): Show | 44 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.192+16961_192+1696 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | ||||||
chr3:142870706
|
A | ATTT | 8 | a0001c0001t0001g0117a0001c0001t0001g0263a0001c0001t0001g0267others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+16960_192+1696 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | ||||||
chr3:142870706
|
A | ATTTT | 14 | a0001c0001t0001g0154a0001c0001t0001g0182a0001c0001t0001g0252others(11): Show | 14 | HG01175.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+16959_192+1696 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | ||||||
chr3:142870784
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+16885G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870784 | ||||||
chr3:142871082
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+16587G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871082 | ||||||
chr3:142871154
|
C | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+16515G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871154 | ||||||
chr3:142871186
|
C | G | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | NA18944.hp2 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+16483G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871186 | ||||||
chr3:142871383
|
T | C | 1 | a0001c0001t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.192+16286A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871383 | ||||||
chr3:142871519
|
G | C | 14 | a0001c0001t0002g0018a0001c0001t0002g0120a0001c0001t0002g0231others(11): Show | 15 | HG00423.hp2 HG01934.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+16150C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871519 | ||||||
chr3:142871543
|
G | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(37): Show | 43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+16126C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871543 | ||||||
chr3:142871671
|
C | T | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192+15998G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871671 | ||||||
chr3:142871675
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+15994T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871675 | ||||||
chr3:142871819
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(87): Show | 94 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.192+15850G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871819 | ||||||
chr3:142871832
|
G | A | 2 | a0001c0001t0002g0264a0001c0001t0002g0265 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192+15837C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871832 | ||||||
chr3:142871877
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+15792A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871877 | ||||||
chr3:142872252
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.192+15417T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872252 | ||||||
chr3:142872332
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.192+15337C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872332 | ||||||
chr3:142872392
|
T | C | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+15277A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872392 | ||||||
chr3:142872455
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+15214G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872455 | ||||||
chr3:142872685
|
C | T | 19 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0182others(16): Show | 19 | HG01175.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.192+14984G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872685 | ||||||
chr3:142872701
|
C | T | 1 | a0001c0007t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.192+14968G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872701 | ||||||
chr3:142872728
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(8): Show | 14 | HG00438.hp1 HG00673.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+14941G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872728 | ||||||
chr3:142872778
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+14891A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872778 | ||||||
chr3:142872873
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+14796A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872873 | ||||||
chr3:142872889
|
A | C | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+14780T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872889 | ||||||
chr3:142873023
|
T | C | 1 | a0001c0001t0002g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.192+14646A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873023 | ||||||
chr3:142873114
|
T | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(37): Show | 43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+14555A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873114 | ||||||
chr3:142873166
|
C | T | 1 | a0001c0001t0006g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.192+14503G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873166 | ||||||
chr3:142873177
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+14492A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873177 | ||||||
chr3:142873283
|
T | A | 1 | a0001c0001t0002g0303 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192+14386A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873283 | ||||||
chr3:142873332
|
G | T | 1 | a0001c0001t0006g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192+14337C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873332 | ||||||
chr3:142873347
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0006g0084 | 2 | HG01952.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.192+14322G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873347 | ||||||
chr3:142873355
|
T | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0290a0001c0001t0002g0291 | 3 | HG00323.hp2 HG01496.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.192+14314A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873355 | ||||||
chr3:142873367
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(18): Show | 24 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+14302G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873367 | ||||||
chr3:142873375
|
T | C | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+14294A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873375 | ||||||
chr3:142873393
|
C | CA | 11 | a0001c0001t0001g0104a0001c0001t0001g0141a0001c0001t0001g0238others(8): Show | 11 | HG00642.hp1 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+14275dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873393 | ||||||
chr3:142873407
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0311 | 2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+14262T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873407 | ||||||
chr3:142873418
|
T | A | 7 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG00642.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+14251A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873418 | ||||||
chr3:142873424
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0002g0140others(14): Show | 20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+14245T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873424 | ||||||
chr3:142873539
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0145others(3): Show | 6 | HG01109.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+14130C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873539 | ||||||
chr3:142873714
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(18): Show | 24 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+13955G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873714 | ||||||
chr3:142873781
|
G | T | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+13888C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873781 | ||||||
chr3:142873786
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+13883A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873786 | ||||||
chr3:142873825
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192+13844G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873825 | ||||||
chr3:142873925
|
C | T | 5 | a0001c0001t0005g0062a0003c0003t0001g0259a0003c0003t0003g0053others(2): Show | 5 | HG01074.hp1 HG01099.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+13744G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873925 | ||||||
chr3:142873998
|
G | C | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+13671C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873998 | ||||||
chr3:142874169
|
G | A | 4 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0025others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+13500C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874169 | ||||||
chr3:142874207
|
T | A | 1 | a0001c0001t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.192+13462A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874207 | ||||||
chr3:142874265
|
G | T | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.192+13404C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874265 | ||||||
chr3:142874345
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+13324T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874345 | ||||||
chr3:142874428
|
C | T | 2 | a0001c0001t0003g0060a0001c0001t0003g0061 | 2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.192+13241G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874428 | ||||||
chr3:142874429
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+13240C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874429 | ||||||
chr3:142874548
|
T | C | 17 | a0001c0001t0001g0166a0001c0001t0001g0242a0001c0001t0002g0292others(14): Show | 19 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.192+13121A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874548 | ||||||
chr3:142874853
|
G | A | 1 | a0001c0001t0006g0084 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+12816C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874853 | ||||||
chr3:142875113
|
T | C | 7 | a0001c0001t0005g0002a0001c0001t0005g0032a0001c0001t0005g0062others(4): Show | 8 | HG01074.hp1 HG01099.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+12556A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875113 | ||||||
chr3:142875224
|
C | A | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+12445G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875224 | ||||||
chr3:142875326
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+12343G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875326 | ||||||
chr3:142875443
|
T | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0252others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+12226A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875443 | ||||||
chr3:142875445
|
A | C | 2 | a0002c0002t0001g0169a0002c0002t0001g0170 | 2 | NA19070.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.192+12224T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875445 | ||||||
chr3:142875474
|
T | TGG | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+12194_192+1219 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875474 | ||||||
chr3:142875669
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+12000G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875669 | ||||||
chr3:142876097
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0002g0239a0001c0001t0002g0257 | 3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+11572G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876097 | ||||||
chr3:142876144
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+11525A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876144 | ||||||
chr3:142876317
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.192+11352C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876317 | ||||||
chr3:142876327
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(40): Show | 46 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+11342G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876327 | ||||||
chr3:142876356
|
GAGGT | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+11309_192+1131 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876356 | ||||||
chr3:142876444
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.192+11225C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876444 | ||||||
chr3:142876538
|
G | C | 1 | a0001c0001t0002g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.192+11131C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876538 | ||||||
chr3:142876657
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+11012G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876657 | ||||||
chr3:142876950
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+10719G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876950 | ||||||
chr3:142876985
|
C | G | 12 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0252others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+10684G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876985 | ||||||
chr3:142876992
|
T | C | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+10677A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876992 | ||||||
chr3:142877015
|
T | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(37): Show | 43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+10654A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877015 | ||||||
chr3:142877205
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.192+10464G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877205 | ||||||
chr3:142877219
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.192+10450G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877219 | ||||||
chr3:142877338
|
T | C | 2 | a0001c0001t0002g0193a0001c0001t0002g0232 | 2 | HG01433.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.192+10331A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877338 | ||||||
chr3:142877370
|
C | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(37): Show | 43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+10299G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877370 | ||||||
chr3:142877634
|
T | A | 2 | a0001c0001t0002g0292a0001c0001t0003g0038 | 2 | HG00639.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.192+10035A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877634 | ||||||
chr3:142877637
|
C | A | 1 | a0001c0001t0003g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.192+10032G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877637 | ||||||
chr3:142877818
|
A | T | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+9851T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877818 | ||||||
chr3:142877834
|
C | T | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG01884.hp2 HG02735.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+9835G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877834 | ||||||
chr3:142877933
|
G | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0263others(17): Show | 23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+9736C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877933 | ||||||
chr3:142878081
|
A | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0114others(69): Show | 75 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.192+9588T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878081 | ||||||
chr3:142878365
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.192+9304G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878365 | ||||||
chr3:142878662
|
T | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0104others(85): Show | 92 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.192+9007A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878662 | ||||||
chr3:142878721
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.192+8948C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878721 | ||||||
chr3:142878852
|
C | CA | 25 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0154others(22): Show | 25 | HG00735.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.192+8816dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878852 | ||||||
chr3:142879125
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0003g0001others(15): Show | 21 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.192+8544G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879125 | ||||||
chr3:142879290
|
G | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0117a0001c0001t0001g0118others(40): Show | 46 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+8379C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879290 | ||||||
chr3:142879307
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0002g0144a0001c0001t0002g0146 | 3 | HG02615.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.192+8362G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879307 | ||||||
chr3:142879372
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.192+8297C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879372 | ||||||
chr3:142879421
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+8248G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879421 | ||||||
chr3:142879691
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.192+7978G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879691 | ||||||
chr3:142879720
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | NA18944.hp1 NA18961.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+7949C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879720 | ||||||
chr3:142879724
|
C | A | 21 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0171others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+7945G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879724 | ||||||
chr3:142879725
|
T | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0252others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+7944A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879725 | ||||||
chr3:142879736
|
G | A | 150 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(147): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.192+7933C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879736 | ||||||
chr3:142879740
|
A | C | 1 | a0001c0001t0004g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.192+7929T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879740 | ||||||
chr3:142879740
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.192+7929T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879740 | ||||||
chr3:142879765
|
C | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG02280.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+7904G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879765 | ||||||
chr3:142879785
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+7884G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879785 | ||||||
chr3:142879796
|
C | T | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0005g0062others(1): Show | 4 | HG02074.hp2 HG02083.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+7873G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879796 | ||||||
chr3:142879797
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0156a0001c0001t0002g0303 | 4 | HG02056.hp2 HG02071.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+7872C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879797 | ||||||
chr3:142879798
|
C | T | 6 | a0001c0001t0002g0018a0001c0001t0002g0156a0001c0001t0002g0303others(3): Show | 8 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+7871G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879798 | ||||||
chr3:142879805
|
TA | T | 9 | a0001c0001t0001g0141a0001c0001t0002g0018a0001c0001t0002g0156others(6): Show | 11 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+7863delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879805 | ||||||
chr3:142879830
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0311a0001c0001t0002g0275 | 3 | HG01175.hp2 HG02132.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+7839G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879830 | ||||||
chr3:142879970
|
C | CA | 8 | a0001c0001t0001g0166a0001c0001t0001g0185a0001c0001t0001g0238others(5): Show | 8 | HG02027.hp2 HG02602.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+7698dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | ||||||
chr3:142879970
|
CA | C | 13 | a0001c0001t0001g0105a0001c0001t0001g0305a0001c0001t0002g0196others(10): Show | 13 | HG00544.hp1 HG02074.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+7698delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | ||||||
chr3:142879970
|
CAA | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0137a0001c0001t0001g0138others(30): Show | 34 | HG01109.hp2 HG01433.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.192+7697_192+7698d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | ||||||
chr3:142879970
|
CAAA | C | 37 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0115others(34): Show | 37 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.192+7696_192+7698d others(5): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | ||||||
chr3:142880043
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.192+7626G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880043 | ||||||
chr3:142880050
|
C | G | 9 | a0001c0001t0003g0023a0001c0001t0003g0026a0001c0001t0005g0025others(6): Show | 9 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+7619G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880050 | ||||||
chr3:142880061
|
C | A | 3 | a0001c0001t0001g0261a0001c0001t0002g0264a0001c0001t0002g0265 | 3 | HG02622.hp2 HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.192+7608G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880061 | ||||||
chr3:142880107
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.192+7562T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880107 | ||||||
chr3:142880146
|
C | T | 13 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0145others(10): Show | 13 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+7523G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880146 | ||||||
chr3:142880233
|
T | C | 2 | a0001c0001t0002g0239a0001c0001t0002g0257 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+7436A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880233 | ||||||
chr3:142880238
|
T | TA | 8 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(5): Show | 8 | HG01175.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+7430dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880238 | ||||||
chr3:142880238
|
TA | T | 19 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0143others(16): Show | 20 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+7430delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880238 | ||||||
chr3:142880274
|
T | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0001t0001g0148others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+7395A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880274 | ||||||
chr3:142880282
|
T | G | 1 | a0001c0001t0002g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192+7387A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880282 | ||||||
chr3:142880332
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0171 | 3 | HG01109.hp2 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.192+7337T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880332 | ||||||
chr3:142880406
|
AC | A | 17 | a0001c0001t0001g0115a0001c0001t0001g0122a0001c0001t0001g0123others(14): Show | 17 | HG00642.hp2 HG01243.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.192+7262delG | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880406 | ||||||
chr3:142880443
|
C | T | 62 | a0001c0001t0001g0006a0001c0001t0001g0114a0001c0001t0001g0115others(59): Show | 63 | HG00642.hp1 HG00642.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.192+7226G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880443 | ||||||
chr3:142880464
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0002g0155 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.192+7205T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880464 | ||||||
chr3:142880522
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+7147T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880522 | ||||||
chr3:142880581
|
T | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0119a0001c0001t0001g0136others(47): Show | 53 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.192+7088A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880581 | ||||||
chr3:142880593
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0119a0001c0001t0001g0136others(35): Show | 41 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.192+7076G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880593 | ||||||
chr3:142880760
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.192+6909G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880760 | ||||||
chr3:142880811
|
C | T | 1 | a0001c0001t0003g0001 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.192+6858G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880811 | ||||||
chr3:142880846
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0136others(20): Show | 25 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.192+6823T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880846 | ||||||
chr3:142880978
|
C | T | 266 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.192+6691G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880978 | ||||||
chr3:142881235
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.192+6434G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881235 | ||||||
chr3:142881245
|
T | C | 272 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.192+6424A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881245 | ||||||
chr3:142881410
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0114others(59): Show | 65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+6259T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881410 | ||||||
chr3:142881558
|
A | C | 1 | a0001c0001t0002g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.192+6111T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881558 | ||||||
chr3:142881614
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+6055T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881614 | ||||||
chr3:142881646
|
T | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0263 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.192+6023A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881646 | ||||||
chr3:142881764
|
T | TA | 10 | a0001c0001t0001g0136a0001c0001t0001g0299a0001c0001t0001g0300others(7): Show | 11 | HG02056.hp2 HG02071.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+5904dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881764 | ||||||
chr3:142881827
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0242a0001c0001t0004g0065others(35): Show | 40 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.192+5842C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881827 | ||||||
chr3:142881833
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0114others(56): Show | 62 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.192+5836G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881833 | ||||||
chr3:142881882
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.192+5787C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881882 | ||||||
chr3:142882141
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+5528G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882141 | ||||||
chr3:142882193
|
C | A | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5476G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882193 | ||||||
chr3:142882199
|
T | TA | 114 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0104others(111): Show | 120 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.192+5469dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882199 | ||||||
chr3:142882226
|
G | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+5443C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882226 | ||||||
chr3:142882417
|
T | A | 122 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0104others(119): Show | 128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.192+5252A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882417 | ||||||
chr3:142882453
|
G | A | 2 | a0001c0001t0001g0243a0004c0005t0001g0244 | 2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.192+5216C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882453 | ||||||
chr3:142882587
|
A | ATTATTAT others(17): Show |
1 | a0002c0002t0002g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.192+5081_192+5082i others(26): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882587 | ||||||
chr3:142882587
|
A | ATTATTAT others(27): Show |
1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.192+5081_192+5082i others(36): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882587 | ||||||
chr3:142882589
|
A | T | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5080T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882589 | ||||||
chr3:142882590
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0141a0002c0002t0002g0142 | 3 | HG02615.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5079G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882590 | ||||||
chr3:142882594
|
A | T | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5075T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882594 | ||||||
chr3:142882599
|
A | C | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5070T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882599 | ||||||
chr3:142882601
|
A | G | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5068T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882601 | ||||||
chr3:142882602
|
G | A | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5067C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882602 | ||||||
chr3:142882603
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.192+5066C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882603 | ||||||
chr3:142882608
|
A | G | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5061T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882608 | ||||||
chr3:142882615
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.192+5054G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882615 | ||||||
chr3:142882616
|
G | A | 3 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0061 | 3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.192+5053C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882616 | ||||||
chr3:142882622
|
C | G | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5047G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882622 | ||||||
chr3:142882943
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0263others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+4726C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882943 | ||||||
chr3:142883124
|
T | C | 1 | a0001c0001t0003g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.192+4545A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883124 | ||||||
chr3:142883130
|
G | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(56): Show | 61 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.192+4539C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883130 | ||||||
chr3:142883156
|
G | A | 1 | a0002c0002t0001g0152 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.192+4513C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883156 | ||||||
chr3:142883198
|
C | CA | 30 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0137others(27): Show | 31 | HG00544.hp1 HG00597.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.192+4470dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | ||||||
chr3:142883198
|
C | CAA | 56 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(53): Show | 58 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.192+4469_192+4470d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | ||||||
chr3:142883198
|
CA | C | 49 | a0001c0001t0001g0141a0001c0001t0001g0258a0001c0001t0003g0001others(46): Show | 52 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.192+4470delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | ||||||
chr3:142883198
|
CAAAAA | C | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0108others(7): Show | 10 | HG00597.hp1 HG02083.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+4466_192+4470d others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | ||||||
chr3:142883363
|
C | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(58): Show | 63 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.192+4306G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883363 | ||||||
chr3:142883393
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+4276G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883393 | ||||||
chr3:142883402
|
T | G | 1 | a0001c0001t0002g0253 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.192+4267A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883402 | ||||||
chr3:142883426
|
T | C | 59 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(56): Show | 61 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.192+4243A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883426 | ||||||
chr3:142883598
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0145a0001c0001t0001g0148others(9): Show | 13 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+4071A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883598 | ||||||
chr3:142883625
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+4044C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883625 | ||||||
chr3:142883709
|
A | AC | 63 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(60): Show | 65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3959_192+3960i others(3): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883709 | ||||||
chr3:142883711
|
A | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0171a0001c0001t0001g0172others(15): Show | 19 | HG00738.hp1 HG01175.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.192+3958T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883711 | ||||||
chr3:142883822
|
G | C | 2 | a0001c0001t0003g0060a0001c0001t0003g0061 | 2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.192+3847C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883822 | ||||||
chr3:142883824
|
C | T | 47 | a0001c0001t0001g0153a0001c0001t0001g0258a0001c0001t0003g0001others(44): Show | 50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+3845G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883824 | ||||||
chr3:142883858
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(60): Show | 65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3811G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883858 | ||||||
chr3:142883893
|
A | G | 4 | a0001c0004t0001g0322a0001c0004t0001g0323a0001c0004t0002g0320others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+3776T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883893 | ||||||
chr3:142883902
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(60): Show | 65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3767G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883902 | ||||||
chr3:142883911
|
C | T | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+3758G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883911 | ||||||
chr3:142883950
|
G | C | 1 | a0001c0001t0001g0310 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.192+3719C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883950 | ||||||
chr3:142883971
|
T | C | 2 | a0001c0001t0001g0141a0002c0002t0002g0142 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+3698A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883971 | ||||||
chr3:142884193
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+3476A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884193 | ||||||
chr3:142884210
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.192+3459C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884210 | ||||||
chr3:142884268
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(60): Show | 65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3401C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884268 | ||||||
chr3:142884312
|
C | A | 9 | a0001c0001t0004g0085a0001c0001t0004g0087a0001c0001t0004g0088others(6): Show | 9 | HG00423.hp2 HG01934.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+3357G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884312 | ||||||
chr3:142884386
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0143a0001c0001t0001g0145others(14): Show | 18 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+3283G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884386 | ||||||
chr3:142884458
|
C | G | 2 | a0001c0001t0003g0021a0001c0001t0003g0022 | 2 | NA18948.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.192+3211G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884458 | ||||||
chr3:142884560
|
T | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+3109A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884560 | ||||||
chr3:142884628
|
T | C | 266 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 282 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.192+3041A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884628 | ||||||
chr3:142884858
|
A | G | 1 | a0001c0001t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.192+2811T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884858 | ||||||
chr3:142884928
|
T | C | 3 | a0001c0001t0001g0256a0001c0001t0002g0255a0001c0001t0002g0257 | 3 | HG03195.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.192+2741A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884928 | ||||||
chr3:142884950
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.192+2719C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884950 | ||||||
chr3:142885019
|
T | A | 47 | a0001c0001t0001g0153a0001c0001t0001g0258a0001c0001t0003g0001others(44): Show | 50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+2650A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885019 | ||||||
chr3:142885021
|
TA | T | 47 | a0001c0001t0001g0153a0001c0001t0001g0258a0001c0001t0003g0001others(44): Show | 50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+2647delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885021 | ||||||
chr3:142885023
|
A | T | 47 | a0001c0001t0001g0153a0001c0001t0001g0258a0001c0001t0003g0001others(44): Show | 50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+2646T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885023 | ||||||
chr3:142885062
|
T | A | 4 | a0001c0004t0001g0322a0001c0004t0001g0323a0001c0004t0002g0320others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+2607A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885062 | ||||||
chr3:142885073
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0105others(125): Show | 133 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.192+2596T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885073 | ||||||
chr3:142885086
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+2583C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885086 | ||||||
chr3:142885156
|
A | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0002g0270 | 3 | NA18982.hp1 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.192+2513T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885156 | ||||||
chr3:142885185
|
G | C | 269 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 285 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.192+2484C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885185 | ||||||
chr3:142885295
|
A | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(112): Show | 125 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.192+2374T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885295 | ||||||
chr3:142885634
|
G | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 220 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.192+2035C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885634 | ||||||
chr3:142885684
|
T | A | 3 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0061 | 3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.192+1985A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885684 | ||||||
chr3:142885745
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(251): Show | 269 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.192+1924T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885745 | ||||||
chr3:142885965
|
C | A | 4 | a0001c0004t0001g0322a0001c0004t0001g0323a0001c0004t0002g0320others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1704G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885965 | ||||||
chr3:142886005
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.192+1664T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886005 | ||||||
chr3:142886054
|
C | T | 42 | a0001c0001t0004g0065a0001c0001t0004g0068a0001c0001t0004g0069others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+1615G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886054 | ||||||
chr3:142886145
|
T | C | 1 | a0001c0001t0002g0312 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.192+1524A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886145 | ||||||
chr3:142886220
|
G | T | 1 | a0001c0001t0002g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.192+1449C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886220 | ||||||
chr3:142886304
|
T | C | 48 | a0001c0001t0001g0153a0001c0001t0003g0001a0001c0001t0003g0003others(45): Show | 51 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.192+1365A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886304 | ||||||
chr3:142886365
|
T | C | 2 | a0001c0001t0001g0016a0003c0003t0001g0259 | 3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.192+1304A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886365 | ||||||
chr3:142886375
|
T | TAAAACAC others(305): Show |
1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+1293_192+1294i others(314): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886375 | ||||||
chr3:142886375
|
T | TAAAACAC others(311): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192+1293_192+1294i others(320): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886375 | ||||||
chr3:142886375
|
T | TAAAACAC others(312): Show |
1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.192+1293_192+1294i others(321): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886375 | ||||||
chr3:142886391
|
C | T | 255 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(252): Show | 270 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.192+1278G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886391 | ||||||
chr3:142886478
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+1191G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886478 | ||||||
chr3:142886548
|
C | T | 42 | a0001c0001t0004g0065a0001c0001t0004g0068a0001c0001t0004g0069others(39): Show | 43 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+1121G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886548 | ||||||
chr3:142886593
|
A | G | 1 | a0001c0001t0003g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.192+1076T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886593 | ||||||
chr3:142886607
|
A | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.192+1062T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886607 | ||||||
chr3:142886714
|
G | A | 48 | a0001c0001t0001g0153a0001c0001t0003g0001a0001c0001t0003g0003others(45): Show | 51 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.192+955C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886714 | ||||||
chr3:142886716
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+953A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886716 | ||||||
chr3:142886938
|
C | T | 270 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 286 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.192+731G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886938 | ||||||
chr3:142886996
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 6 | HG00639.hp2 HG01081.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+673A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886996 | ||||||
chr3:142887156
|
A | AC | 116 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(113): Show | 126 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.192+512dupG | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887156 | ||||||
chr3:142887220
|
G | A | 2 | a0001c0001t0005g0062a0003c0003t0003g0063 | 2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.192+449C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887220 | ||||||
chr3:142887228
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0002g0155 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.192+441A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887228 | ||||||
chr3:142887319
|
C | A | 8 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(5): Show | 8 | HG00544.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+350G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887319 | ||||||
chr3:142887489
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+180C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887489 | ||||||
chr3:142887574
|
C | G | 2 | a0001c0001t0002g0140a0002c0002t0007g0139 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.192+95G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887574 | ||||||
chr3:142887643
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+26T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887643 | ||||||
chr3:142887651
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.192+18A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887651 | ||||||
chr3:142887865
|
T | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.84-88A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142887865 | ||||||
chr3:142888071
|
A | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0157a0001c0001t0001g0158others(8): Show | 12 | HG00673.hp2 HG02602.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.84-294T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888071 | ||||||
chr3:142888100
|
G | C | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(114): Show | 127 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.84-323C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888100 | ||||||
chr3:142888425
|
G | C | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.83+389C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888425 | ||||||
chr3:142888430
|
A | G | 26 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0115others(23): Show | 27 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+384T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888430 | ||||||
chr3:142888454
|
A | C | 12 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0108others(9): Show | 12 | HG00597.hp1 HG02083.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.83+360T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888454 | ||||||
chr3:142888515
|
C | A | 1 | a0001c0001t0002g0317 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.83+299G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888515 | ||||||
chr3:142888645
|
C | G | 265 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.83+169G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888645 | ||||||
chr3:142888646
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.83+168C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888646 |