geneid | 728537 |
---|---|
ensemblid | ENSG00000228486.11 |
hgncid | 49272 |
symbol | C2orf92 |
name | chromosome 2 open reading frame 92 |
refseq_nuc | NM_001351368.2 |
refseq_prot | NP_001338297.1 |
ensembl_nuc | ENST00000627399.4 |
ensembl_prot | ENSP00000490587.1 |
mane_status | MANE Select |
chr | chr2 |
start | 97669713 |
end | 97703066 |
strand | + |
ver | v1.2 |
region | chr2:97669713-97703066 |
region5000 | chr2:97664713-97708066 |
regionname0 | C2orf92_chr2_97669713_97703066 |
regionname5000 | C2orf92_chr2_97664713_97708066 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 265 | 172 | 65 | 31 | 52 | 3 | 19 | 42 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0002 | 0/0 | 265 | 86 | 9 | 23 | 41 | 5 | 8 | 31 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0003 | 0/0 | 265 | 29 | 1 | 2 | 23 | 0 | 3 | 17 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0004 | 0/0 | 258 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0005 | 0/0 | 265 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0006 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0007 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0008 | 0/0 | 265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0009 | 0/0 | 254 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0010 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0011 | 0/0 | 264 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 798 | 172 | 65 | 31 | 52 | 3 | 19 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0002 | 0/0 | 798 | 83 | 9 | 23 | 38 | 5 | 8 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0003 | 0/0 | 798 | 29 | 1 | 2 | 23 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0004 | 0/0 | 797 | 14 | 12 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0005 | 0/0 | 798 | 3 | 0 | 0 | 3 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0006 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0007 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0008 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0009 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0010 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0011 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
c0012 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 342 | 167 | 72 | 37 | 43 | 6 | 9 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
t0002 | 1/1 | 342 | 115 | 21 | 21 | 51 | 2 | 18 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
t0003 | 0/0 | 342 | 18 | 0 | 0 | 18 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
t0004 | 0/0 | 342 | 7 | 0 | 0 | 4 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
t0005 | 0/0 | 342 | 3 | 1 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 2 | 2 | 11 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0002 | 0/0 | 16 | 0 | 4 | 9 | 2 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0004 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 798 | 172 | 65 | 31 | 52 | 3 | 19 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0002c0002 | 0/0 | 798 | 83 | 9 | 23 | 38 | 5 | 8 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0002c0005 | 0/0 | 798 | 3 | 0 | 0 | 3 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0003c0003 | 0/0 | 798 | 29 | 1 | 2 | 23 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0004c0004 | 0/0 | 797 | 14 | 12 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0005c0006 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0006c0010 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0007c0008 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0008c0009 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0009c0011 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0010c0012 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0011c0007 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1139 | 63 | 50 | 10 | 1 | 1 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0001c0001t0002 | 1/1 | 1139 | 109 | 15 | 21 | 51 | 2 | 18 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0002c0002t0001 | 0/0 | 1139 | 83 | 9 | 23 | 38 | 5 | 8 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0002c0005t0001 | 0/0 | 1139 | 3 | 0 | 0 | 3 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0003c0003t0001 | 0/0 | 1139 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0003c0003t0003 | 0/0 | 1139 | 17 | 0 | 0 | 17 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0003c0003t0004 | 0/0 | 1139 | 7 | 0 | 0 | 4 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0003c0003t0005 | 0/0 | 1139 | 3 | 1 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0004c0004t0001 | 0/0 | 1138 | 14 | 12 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0005c0006t0002 | 0/0 | 1139 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0006c0010t0001 | 0/0 | 1138 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0007c0008t0002 | 0/0 | 1139 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0008c0009t0002 | 0/0 | 1139 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0009c0011t0002 | 0/0 | 1106 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0010c0012t0003 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
a0011c0007t0001 | 0/0 | 1136 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | copy fasta | chr2 | 97664713 | 97708066 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0001 | 0/0 | 18 | 2 | 2 | 11 | 0 | 3 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0002 | 0/0 | 16 | 0 | 4 | 9 | 2 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0004 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0002c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0003c0003t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0004c0004t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0005c0006t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0005c0006t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0006c0010t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0007c0008t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0008c0009t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0009c0011t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0010c0012t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
a0011c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0060 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | GBR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00597 | hp2 | a0003 | c0003 | t0003 | g0224 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | CHS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01243 | hp1 | a0004 | c0004 | t0001 | g0092 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0039 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01358 | hp1 | a0004 | c0004 | t0001 | g0082 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0038 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0075 | EUR | IBS | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02040 | hp2 | a0003 | c0003 | t0005 | g0095 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02056 | hp1 | a0003 | c0003 | t0004 | g0103 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02056 | hp2 | a0003 | c0003 | t0004 | g0097 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02071 | hp1 | a0003 | c0003 | t0004 | g0098 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02083 | hp1 | a0003 | c0003 | t0004 | g0099 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02451 | hp1 | a0004 | c0004 | t0001 | g0084 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02717 | hp2 | a0005 | c0006 | t0002 | g0146 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02895 | hp1 | a0009 | c0011 | t0002 | g0172 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02895 | hp2 | a0004 | c0004 | t0001 | g0085 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02897 | hp1 | a0004 | c0004 | t0001 | g0087 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02965 | hp2 | a0005 | c0006 | t0002 | g0022 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02970 | hp2 | a0004 | c0004 | t0001 | g0083 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03098 | hp1 | a0004 | c0004 | t0001 | g0081 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03130 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0086 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03225 | hp1 | a0005 | c0006 | t0002 | g0022 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03453 | hp1 | a0004 | c0004 | t0001 | g0088 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03453 | hp2 | a0004 | c0004 | t0001 | g0090 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03486 | hp2 | a0003 | c0003 | t0005 | g0096 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03579 | hp1 | a0004 | c0004 | t0001 | g0080 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03834 | hp1 | a0003 | c0003 | t0004 | g0102 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG04115 | hp1 | a0003 | c0003 | t0004 | g0101 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG04204 | hp2 | a0003 | c0003 | t0004 | g0100 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | STU | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18906 | hp2 | a0004 | c0004 | t0001 | g0091 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18940 | hp1 | a0003 | c0003 | t0003 | g0231 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18941 | hp2 | a0010 | c0012 | t0003 | g0012 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18947 | hp1 | a0002 | c0005 | t0001 | g0062 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18951 | hp1 | a0003 | c0003 | t0003 | g0232 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18956 | hp2 | a0003 | c0003 | t0003 | g0226 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18960 | hp1 | a0002 | c0005 | t0001 | g0036 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18965 | hp2 | a0003 | c0003 | t0003 | g0227 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18966 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18966 | hp2 | a0011 | c0007 | t0001 | g0094 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18967 | hp2 | a0003 | c0003 | t0003 | g0225 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18970 | hp2 | a0003 | c0003 | t0003 | g0228 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18971 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18973 | hp1 | a0003 | c0003 | t0003 | g0233 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18983 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18999 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19010 | hp1 | a0002 | c0005 | t0001 | g0035 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19043 | hp1 | a0006 | c0010 | t0001 | g0079 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19054 | hp2 | a0003 | c0003 | t0003 | g0229 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19070 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19083 | hp1 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19084 | hp1 | a0003 | c0003 | t0005 | g0234 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19085 | hp1 | a0003 | c0003 | t0003 | g0230 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19088 | hp1 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ASW | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA20129 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | ASW | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | GIH | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
HG06807 | hp2 | a0008 | c0009 | t0002 | g0183 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | USA | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
NA21309 | hp2 | a0007 | c0008 | t0002 | g0174 | AFR | LWK | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0200 | REF | REF | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0206 | REF | REF | C2orf92_chr2_97664713_97708066 | C2orf92 | chr2 | 97664713 | 97708066 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97690264
|
A | G | 3 | a0003a0004a0010 | 44 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(41): Show |
missense_variant | MODERATE | c.340A>G | p.Ile114Val | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/8 | 416/1139 | 340/798 | 114/265 | chr2 | 97690264 | ||
chr2:97699070
|
G | A | 1 | a0010 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.448G>A | p.Asp150Asn | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/8 | 524/1139 | 448/798 | 150/265 | chr2 | 97699070 | ||
chr2:97701148
|
ATTTAGAT others(31): Show |
A | 1 | a0009 | 1 | HG02895.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.515-3_549delTAGATG others(32): Show |
p.Asp172fs | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 515/798 | 172/265 | INFO_REALIGN_3_PRIME | chr2 | 97701148 | ||
chr2:97701202
|
A | T | 2 | a0004a0006 | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
missense_variant | MODERATE | c.563A>T | p.Gln188Leu | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 639/1139 | 563/798 | 188/265 | chr2 | 97701202 | ||
chr2:97701222
|
G | A | 2 | a0002a0011 | 87 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(84): Show |
missense_variant | MODERATE | c.583G>A | p.Ala195Thr | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 659/1139 | 583/798 | 195/265 | chr2 | 97701222 | ||
chr2:97701225
|
G | A | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.586G>A | p.Val196Ile | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/8 | 662/1139 | 586/798 | 196/265 | chr2 | 97701225 | ||
chr2:97702728
|
A | C | 1 | a0005 | 3 | HG02717.hp2 HG02965.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.725A>C | p.His242Pro | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 801/1139 | 725/798 | 242/265 | chr2 | 97702728 | ||
chr2:97702739
|
GA | G | 2 | a0004a0006 | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
frameshift_variant | HIGH | c.743delA | p.Asn248fs | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 819/1139 | 743/798 | 248/265 | INFO_REALIGN_3_PRIME | chr2 | 97702739 | |
chr2:97702758
|
T | C | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.755T>C | p.Leu252Pro | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 831/1139 | 755/798 | 252/265 | chr2 | 97702758 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97674490
|
G | A | 1 | a0002c0005 | 3 | NA18947.hp1 NA18960.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.81G>A | p.Pro27Pro | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/8 | 157/1139 | 81/798 | 27/265 | chr2 | 97674490 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97669772
|
T | C | 11 | a0001c0001t0001a0002c0002t0001a0002c0005t0001others(8): Show | 195 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(192): Show |
5_prime_UTR_variant | MODIFIER | c.-17T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/8 | 17 | chr2 | 97669772 | |||||
chr2:97702887
|
T | C | 1 | a0003c0003t0004 | 7 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*86T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 86 | chr2 | 97702887 | |||||
chr2:97702901
|
G | A | 1 | a0003c0003t0005 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*100G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 100 | chr2 | 97702901 | |||||
chr2:97703015
|
G | A | 3 | a0003c0003t0003a0003c0003t0004a0010c0012t0003 | 25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*214G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 8/8 | 214 | chr2 | 97703015 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:97669979
|
G | T | 1 | a0001c0001t0002g0235 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46+145G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97669979 | ||||||
chr2:97670070
|
C | T | 1 | a0003c0003t0005g0234 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.46+236C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670070 | ||||||
chr2:97670093
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+259G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670093 | ||||||
chr2:97670135
|
A | G | 14 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(11): Show | 18 | HG00597.hp2 NA18940.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+301A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670135 | ||||||
chr2:97670491
|
C | CA | 56 | a0001c0001t0001g0051a0001c0001t0001g0077a0002c0002t0001g0002others(53): Show | 89 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.46+669dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 97670491 | |||||
chr2:97670667
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+833G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670667 | ||||||
chr2:97670933
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+1099A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670933 | ||||||
chr2:97670982
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+1148C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97670982 | ||||||
chr2:97671020
|
T | C | 101 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(98): Show | 140 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.46+1186T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671020 | ||||||
chr2:97671109
|
G | C | 16 | a0001c0001t0001g0089a0001c0001t0001g0093a0004c0004t0001g0018others(13): Show | 17 | HG01243.hp1 HG01261.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.46+1275G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671109 | ||||||
chr2:97671334
|
C | CG | 98 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(95): Show | 134 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.46+1505dupG | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 97671334 | |||||
chr2:97671334
|
C | CGG | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0031others(2): Show | 7 | HG02109.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+1504_46+1505dup others(2): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 97671334 | |||||
chr2:97671437
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+1603G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671437 | ||||||
chr2:97671687
|
A | G | 3 | a0001c0001t0001g0093a0004c0004t0001g0091a0004c0004t0001g0092 | 3 | HG01243.hp1 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.46+1853A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97671687 | ||||||
chr2:97672028
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46+2194A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672028 | ||||||
chr2:97672039
|
G | C | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+2205G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672039 | ||||||
chr2:97672065
|
C | T | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0003c0003t0003g0233 | 3 | HG01168.hp1 HG02738.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.46+2231C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672065 | ||||||
chr2:97672086
|
A | G | 46 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.46+2252A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672086 | ||||||
chr2:97672336
|
G | A | 2 | a0005c0006t0002g0022a0005c0006t0002g0146 | 3 | HG02717.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.47-2120G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672336 | ||||||
chr2:97672388
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47-2068C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672388 | ||||||
chr2:97672459
|
C | T | 1 | a0002c0002t0001g0017 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.47-1997C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672459 | ||||||
chr2:97672679
|
C | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(41): Show | 50 | HG00597.hp2 HG01243.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.47-1777C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672679 | ||||||
chr2:97672734
|
G | A | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.47-1722G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672734 | ||||||
chr2:97672841
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.47-1615C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672841 | ||||||
chr2:97672917
|
A | G | 1 | a0003c0003t0004g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.47-1539A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97672917 | ||||||
chr2:97673217
|
C | T | 7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG01123.hp1 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-1239C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673217 | ||||||
chr2:97673345
|
G | A | 1 | a0002c0002t0001g0007 | 3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.47-1111G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673345 | ||||||
chr2:97673376
|
G | C | 56 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(53): Show | 89 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.47-1080G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673376 | ||||||
chr2:97673534
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.47-922C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673534 | ||||||
chr2:97673625
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.47-831G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673625 | ||||||
chr2:97673719
|
C | T | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.47-737C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97673719 | ||||||
chr2:97674030
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.47-426G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674030 | ||||||
chr2:97674211
|
T | C | 1 | a0002c0002t0001g0034 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.47-245T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674211 | ||||||
chr2:97674261
|
C | A | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.47-195C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674261 | ||||||
chr2:97674398
|
T | C | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.47-58T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 1/7 | chr2 | 97674398 | ||||||
chr2:97674581
|
CAT | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+25_148+26delAT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674581 | ||||||
chr2:97674747
|
A | G | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.148+190A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674747 | ||||||
chr2:97674946
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148+389C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674946 | ||||||
chr2:97674983
|
G | A | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+426G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97674983 | ||||||
chr2:97675139
|
C | T | 1 | a0002c0002t0001g0015 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.148+582C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97675139 | ||||||
chr2:97675272
|
A | C | 21 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(18): Show | 25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.149-573A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 2/7 | chr2 | 97675272 | ||||||
chr2:97675925
|
TTTGGTAA others(49): Show |
T | 1 | a0011c0007t0001g0094 | 1 | NA18966.hp2 | splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.232+1_232+56delGTA others(53): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97675925 | |||||
chr2:97676386
|
A | C | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.232+458A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676386 | ||||||
chr2:97676433
|
C | CA | 6 | a0001c0001t0001g0019a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 7 | HG02257.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+520dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676433 | |||||
chr2:97676448
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.232+520A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676448 | ||||||
chr2:97676448
|
AG | A | 25 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0119others(22): Show | 27 | HG00642.hp1 HG01123.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.232+521delG | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676448 | ||||||
chr2:97676449
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0104others(24): Show | 30 | HG01099.hp2 HG01175.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.232+521G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676449 | ||||||
chr2:97676449
|
G | GA | 7 | a0001c0001t0001g0093a0001c0001t0002g0153a0001c0001t0002g0154others(4): Show | 7 | HG00544.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+538dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676449 | |||||
chr2:97676449
|
GA | G | 36 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0218others(33): Show | 41 | HG01243.hp1 HG01358.hp1 HG02056.hp1 others(38): Show |
intron_variant | MODIFIER | c.232+538delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676449 | |||||
chr2:97676449
|
GAA | G | 49 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(46): Show | 82 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.232+537_232+538del others(2): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676449 | |||||
chr2:97676450
|
A | G | 4 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234others(1): Show | 4 | HG02040.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.232+522A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676450 | ||||||
chr2:97676451
|
A | G | 3 | a0002c0002t0001g0037a0002c0005t0001g0035a0002c0005t0001g0036 | 3 | HG02300.hp2 NA18960.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.232+523A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676451 | ||||||
chr2:97676529
|
T | C | 146 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(143): Show | 190 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.232+601T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676529 | ||||||
chr2:97676697
|
A | C | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.232+769A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676697 | ||||||
chr2:97676721
|
A | G | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.232+793A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676721 | ||||||
chr2:97676737
|
A | T | 1 | a0003c0003t0003g0225 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.232+809A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97676737 | ||||||
chr2:97676777
|
AAAAGAG | A | 40 | a0001c0001t0001g0021a0001c0001t0001g0105a0001c0001t0001g0106others(37): Show | 41 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.232+851_232+856del others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97676777 | |||||
chr2:97677000
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0158 | 3 | HG02055.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.232+1072G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677000 | ||||||
chr2:97677069
|
T | C | 1 | a0002c0002t0001g0034 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.232+1141T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677069 | ||||||
chr2:97677144
|
C | T | 1 | a0002c0002t0001g0076 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.232+1216C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677144 | ||||||
chr2:97677237
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.232+1309G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677237 | ||||||
chr2:97677310
|
A | T | 17 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234others(14): Show | 18 | HG01243.hp1 HG01358.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.232+1382A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677310 | ||||||
chr2:97677520
|
T | C | 54 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(51): Show | 87 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.232+1592T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677520 | ||||||
chr2:97677573
|
A | T | 5 | a0002c0002t0001g0008a0002c0002t0001g0017a0002c0002t0001g0073others(2): Show | 8 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+1645A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677573 | ||||||
chr2:97677663
|
C | G | 1 | a0002c0002t0001g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.232+1735C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677663 | ||||||
chr2:97677915
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.232+1987G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97677915 | ||||||
chr2:97678079
|
A | C | 1 | a0002c0002t0001g0034 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.232+2151A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678079 | ||||||
chr2:97678207
|
T | TA | 7 | a0001c0001t0001g0109a0001c0001t0001g0120a0001c0001t0001g0121others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+2290dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678207 | |||||
chr2:97678278
|
G | GA | 7 | a0001c0001t0001g0105a0001c0001t0001g0110a0002c0002t0001g0016others(4): Show | 8 | HG00544.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.232+2362dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678278 | |||||
chr2:97678629
|
A | G | 1 | a0002c0002t0001g0045 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.232+2701A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678629 | ||||||
chr2:97678708
|
T | G | 38 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(35): Show | 43 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.232+2780T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678708 | ||||||
chr2:97678768
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.232+2840G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678768 | ||||||
chr2:97678807
|
T | TA | 58 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(55): Show | 64 | HG00741.hp1 HG01099.hp2 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.232+2900dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678807 | |||||
chr2:97678807
|
T | TAA | 9 | a0001c0001t0001g0122a0003c0003t0004g0097a0003c0003t0004g0098others(6): Show | 9 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+2899_232+2900d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678807 | |||||
chr2:97678807
|
T | TAAAA | 12 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(9): Show | 16 | HG00597.hp2 NA18940.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.232+2897_232+2900d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678807 | |||||
chr2:97678980
|
GA | G | 21 | a0001c0001t0002g0215a0003c0003t0003g0006a0003c0003t0003g0012others(18): Show | 25 | HG00597.hp2 HG01169.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.232+3067delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97678980 | |||||
chr2:97678991
|
A | G | 1 | a0002c0002t0001g0071 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.232+3063A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97678991 | ||||||
chr2:97679022
|
G | T | 1 | a0001c0001t0002g0214 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.232+3094G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679022 | ||||||
chr2:97679121
|
AAG | A | 21 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(18): Show | 25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.232+3198_232+3199d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97679121 | |||||
chr2:97679174
|
G | GA | 53 | a0001c0001t0001g0051a0002c0002t0001g0002a0002c0002t0001g0003others(50): Show | 86 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.232+3257dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97679174 | |||||
chr2:97679319
|
C | T | 2 | a0004c0004t0001g0091a0004c0004t0001g0092 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.232+3391C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679319 | ||||||
chr2:97679328
|
A | C | 1 | a0002c0002t0001g0069 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.232+3400A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679328 | ||||||
chr2:97679557
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0002g0005a0001c0001t0002g0212others(1): Show | 7 | HG01261.hp1 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+3629C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679557 | ||||||
chr2:97679645
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.232+3717C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679645 | ||||||
chr2:97679735
|
C | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.232+3807C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679735 | ||||||
chr2:97679818
|
C | T | 10 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(7): Show | 11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+3890C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679818 | ||||||
chr2:97679837
|
C | CA | 53 | a0001c0001t0001g0028a0001c0001t0001g0051a0002c0002t0001g0002others(50): Show | 86 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.232+3925dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97679837 | |||||
chr2:97679858
|
A | G | 1 | a0003c0003t0003g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.232+3930A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679858 | ||||||
chr2:97679901
|
A | G | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | NA18951.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.232+3973A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679901 | ||||||
chr2:97679936
|
C | T | 3 | a0003c0003t0004g0100a0003c0003t0004g0101a0003c0003t0004g0102 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.232+4008C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97679936 | ||||||
chr2:97680018
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.232+4090G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680018 | ||||||
chr2:97680083
|
T | G | 1 | a0002c0002t0001g0015 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.232+4155T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680083 | ||||||
chr2:97680159
|
C | T | 1 | a0002c0002t0001g0068 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.232+4231C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680159 | ||||||
chr2:97680198
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232+4270C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680198 | ||||||
chr2:97680251
|
A | T | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.232+4323A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680251 | ||||||
chr2:97680539
|
T | A | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.232+4611T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680539 | ||||||
chr2:97680594
|
T | C | 13 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(10): Show | 14 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.232+4666T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680594 | ||||||
chr2:97680692
|
C | T | 10 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(7): Show | 11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.232+4764C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680692 | ||||||
chr2:97680853
|
G | T | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.232+4925G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680853 | ||||||
chr2:97680923
|
C | CT | 3 | a0003c0003t0004g0100a0003c0003t0004g0101a0003c0003t0004g0102 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.232+4996dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97680923 | |||||
chr2:97680925
|
C | A | 3 | a0003c0003t0004g0100a0003c0003t0004g0101a0003c0003t0004g0102 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.232+4997C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97680925 | ||||||
chr2:97680925
|
C | CA | 4 | a0001c0001t0002g0024a0001c0001t0002g0161a0002c0002t0001g0031others(1): Show | 5 | HG01934.hp1 HG02109.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+5006dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97680925 | |||||
chr2:97681017
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.232+5089G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681017 | ||||||
chr2:97681018
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.232+5090A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681018 | ||||||
chr2:97681090
|
G | A | 2 | a0001c0001t0002g0149a0001c0001t0002g0162 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.232+5162G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681090 | ||||||
chr2:97681106
|
C | CA | 39 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0109others(36): Show | 42 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.232+5205dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | |||||
chr2:97681106
|
C | CAA | 35 | a0001c0001t0001g0021a0001c0001t0001g0077a0001c0001t0001g0106others(32): Show | 37 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.232+5204_232+5205d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | |||||
chr2:97681106
|
C | CAAA | 20 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0139others(17): Show | 24 | HG00597.hp2 HG01175.hp2 HG01981.hp2 others(21): Show |
intron_variant | MODIFIER | c.232+5203_232+5205d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | |||||
chr2:97681106
|
CA | C | 8 | a0001c0001t0001g0030a0001c0001t0002g0207a0001c0001t0002g0208others(5): Show | 8 | HG01070.hp1 HG02896.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+5205delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | |||||
chr2:97681106
|
CAAAAAA | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0108others(1): Show | 7 | HG02257.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.232+5200_232+5205d others(8): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681106 | |||||
chr2:97681165
|
T | TAGA | 235 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(232): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.232+5238_232+5240d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97681165 | |||||
chr2:97681186
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.232+5258A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681186 | ||||||
chr2:97681408
|
A | C | 14 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(11): Show | 14 | HG01099.hp2 HG01123.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.232+5480A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681408 | ||||||
chr2:97681536
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.232+5608C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681536 | ||||||
chr2:97681646
|
C | T | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.232+5718C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681646 | ||||||
chr2:97681675
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0145 | 2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.232+5747G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681675 | ||||||
chr2:97681885
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.232+5957A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681885 | ||||||
chr2:97681930
|
A | C | 1 | a0002c0002t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.232+6002A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681930 | ||||||
chr2:97681962
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0166others(1): Show | 6 | NA18947.hp2 NA18960.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+6034A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97681962 | ||||||
chr2:97682140
|
T | C | 1 | a0002c0002t0001g0073 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.232+6212T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682140 | ||||||
chr2:97682151
|
TAGAA | T | 5 | a0001c0001t0002g0026a0001c0001t0002g0204a0001c0001t0002g0217others(2): Show | 6 | NA18943.hp1 NA18972.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+6226_232+6229d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97682151 | |||||
chr2:97682158
|
C | T | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.232+6230C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682158 | ||||||
chr2:97682567
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-6328A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682567 | ||||||
chr2:97682643
|
A | ATAAAT | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6252_233-6251i others(7): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682643 | ||||||
chr2:97682644
|
G | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6251G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682644 | ||||||
chr2:97682645
|
G | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6250G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682645 | ||||||
chr2:97682648
|
G | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6247G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682648 | ||||||
chr2:97682649
|
G | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6246G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682649 | ||||||
chr2:97682650
|
T | C | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-6245T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682650 | ||||||
chr2:97682667
|
C | T | 1 | a0004c0004t0001g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.233-6228C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682667 | ||||||
chr2:97682769
|
GA | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-6116delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97682769 | |||||
chr2:97682824
|
G | A | 4 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-6071G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682824 | ||||||
chr2:97682861
|
C | T | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.233-6034C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97682861 | ||||||
chr2:97683076
|
C | A | 1 | a0004c0004t0001g0081 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.233-5819C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683076 | ||||||
chr2:97683076
|
C | CCA | 25 | a0001c0001t0001g0077a0001c0001t0001g0122a0001c0001t0001g0123others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.233-5782_233-5781d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
C | CCACA | 33 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(30): Show | 35 | HG01099.hp2 HG01175.hp2 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.233-5784_233-5781d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
C | CCACACA | 64 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(61): Show | 92 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-5786_233-5781d others(8): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
C | CCACACAC others(1): Show |
30 | a0001c0001t0001g0131a0001c0001t0001g0143a0001c0001t0001g0158others(27): Show | 38 | HG01106.hp2 HG01123.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.233-5788_233-5781d others(10): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
C | CCACACAC others(3): Show |
5 | a0001c0001t0001g0140a0001c0001t0001g0144a0002c0002t0001g0066others(2): Show | 5 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-5790_233-5781d others(12): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
C | CCACACAC others(5): Show |
4 | a0003c0003t0003g0223a0003c0003t0003g0232a0004c0004t0001g0092others(1): Show | 4 | HG01243.hp1 NA18951.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.233-5792_233-5781d others(14): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
C | CCACACAC others(7): Show |
1 | a0003c0003t0004g0099 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.233-5794_233-5781d others(16): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683076
|
CCA | C | 9 | a0001c0001t0001g0093a0001c0001t0002g0155a0001c0001t0002g0168others(6): Show | 16 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.233-5782_233-5781d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683076 | |||||
chr2:97683097
|
C | T | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.233-5798C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683097 | ||||||
chr2:97683115
|
A | C | 1 | a0003c0003t0004g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.233-5780A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683115 | ||||||
chr2:97683282
|
A | G | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.233-5613A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683282 | ||||||
chr2:97683319
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.233-5576C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683319 | ||||||
chr2:97683520
|
A | G | 141 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(138): Show | 178 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.233-5375A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683520 | ||||||
chr2:97683538
|
T | TA | 60 | a0001c0001t0001g0093a0001c0001t0002g0150a0002c0002t0001g0002others(57): Show | 86 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.233-5341dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683538 | |||||
chr2:97683538
|
TA | T | 8 | a0002c0002t0001g0078a0003c0003t0004g0097a0003c0003t0004g0098others(5): Show | 8 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.233-5341delA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97683538 | |||||
chr2:97683548
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.233-5347A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683548 | ||||||
chr2:97683704
|
G | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.233-5191G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683704 | ||||||
chr2:97683883
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.233-5012G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683883 | ||||||
chr2:97683926
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.233-4969G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683926 | ||||||
chr2:97683927
|
C | T | 1 | a0002c0002t0001g0061 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.233-4968C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683927 | ||||||
chr2:97683967
|
C | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0125 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.233-4928C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97683967 | ||||||
chr2:97684031
|
A | AT | 40 | a0001c0001t0001g0116a0001c0001t0001g0140a0001c0001t0002g0023others(37): Show | 45 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.233-4842dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684031 | |||||
chr2:97684031
|
A | ATT | 6 | a0001c0001t0002g0157a0001c0001t0002g0189a0001c0001t0002g0203others(3): Show | 6 | HG00140.hp2 HG01175.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-4843_233-4842d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684031 | |||||
chr2:97684031
|
AT | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0030others(21): Show | 26 | HG01243.hp1 HG01358.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.233-4842delT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684031 | |||||
chr2:97684454
|
C | T | 1 | a0002c0002t0001g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.233-4441C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684454 | ||||||
chr2:97684514
|
T | G | 1 | a0001c0001t0002g0025 | 2 | HG00558.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.233-4381T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684514 | ||||||
chr2:97684582
|
T | A | 1 | a0001c0001t0002g0216 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.233-4313T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684582 | ||||||
chr2:97684783
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-4112A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684783 | ||||||
chr2:97684851
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-4044A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684851 | ||||||
chr2:97684924
|
T | A | 1 | a0002c0002t0001g0045 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.233-3971T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684924 | ||||||
chr2:97684936
|
A | AT | 61 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(58): Show | 93 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.233-3954dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97684936 | |||||
chr2:97684936
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233-3959A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684936 | ||||||
chr2:97684942
|
A | T | 144 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(141): Show | 188 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.233-3953A>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97684942 | ||||||
chr2:97685008
|
C | T | 2 | a0004c0004t0001g0091a0004c0004t0001g0092 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.233-3887C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685008 | ||||||
chr2:97685141
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-3754G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685141 | ||||||
chr2:97685195
|
T | C | 38 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(35): Show | 43 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.233-3700T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685195 | ||||||
chr2:97685269
|
C | CT | 10 | a0001c0001t0002g0196a0002c0002t0001g0040a0002c0002t0001g0045others(7): Show | 11 | HG04115.hp2 NA18941.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-3612dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97685269 | |||||
chr2:97685269
|
CT | C | 15 | a0001c0001t0001g0127a0001c0001t0002g0171a0003c0003t0005g0096others(12): Show | 16 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.233-3612delT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 97685269 | |||||
chr2:97685366
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233-3529C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685366 | ||||||
chr2:97685512
|
G | A | 10 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(7): Show | 11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-3383G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685512 | ||||||
chr2:97685673
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.233-3222C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685673 | ||||||
chr2:97685674
|
T | C | 14 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(11): Show | 18 | HG00597.hp2 NA18940.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.233-3221T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685674 | ||||||
chr2:97685701
|
T | A | 1 | a0002c0002t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-3194T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685701 | ||||||
chr2:97685784
|
A | G | 38 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(35): Show | 43 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.233-3111A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685784 | ||||||
chr2:97685824
|
A | G | 5 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG01884.hp1 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-3071A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685824 | ||||||
chr2:97685878
|
T | C | 1 | a0002c0002t0001g0007 | 3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.233-3017T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97685878 | ||||||
chr2:97686315
|
C | A | 1 | a0002c0002t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-2580C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97686315 | ||||||
chr2:97686422
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.233-2473T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97686422 | ||||||
chr2:97686749
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.233-2146C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97686749 | ||||||
chr2:97687144
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233-1751C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687144 | ||||||
chr2:97687148
|
TGAGG | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-1746_233-1743d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687148 | ||||||
chr2:97687153
|
C | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-1742C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687153 | ||||||
chr2:97687272
|
C | T | 22 | a0002c0002t0001g0059a0003c0003t0003g0006a0003c0003t0003g0012others(19): Show | 26 | HG00597.hp2 HG01943.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.233-1623C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687272 | ||||||
chr2:97687673
|
G | A | 1 | a0003c0003t0003g0228 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.233-1222G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687673 | ||||||
chr2:97687736
|
G | A | 1 | a0002c0002t0001g0053 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.233-1159G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687736 | ||||||
chr2:97687752
|
G | A | 1 | a0006c0010t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.233-1143G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687752 | ||||||
chr2:97687851
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.233-1044G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687851 | ||||||
chr2:97687875
|
T | C | 43 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0002g0173others(40): Show | 48 | HG00597.hp2 HG01168.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.233-1020T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687875 | ||||||
chr2:97687900
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.233-995G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687900 | ||||||
chr2:97687977
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.233-918T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97687977 | ||||||
chr2:97688046
|
C | G | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.233-849C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688046 | ||||||
chr2:97688095
|
T | C | 1 | a0007c0008t0002g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.233-800T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688095 | ||||||
chr2:97688213
|
A | G | 39 | a0001c0001t0001g0105a0003c0003t0003g0006a0003c0003t0003g0012others(36): Show | 44 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.233-682A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688213 | ||||||
chr2:97688257
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233-638C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688257 | ||||||
chr2:97688334
|
A | C | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-561A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688334 | ||||||
chr2:97688409
|
G | A | 6 | a0001c0001t0002g0026a0001c0001t0002g0204a0001c0001t0002g0217others(3): Show | 7 | HG01192.hp1 NA18943.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.233-486G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688409 | ||||||
chr2:97688455
|
G | A | 3 | a0002c0005t0001g0035a0002c0005t0001g0036a0002c0005t0001g0062 | 3 | NA18947.hp1 NA18960.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.233-440G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688455 | ||||||
chr2:97688649
|
G | A | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.233-246G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688649 | ||||||
chr2:97688785
|
C | T | 1 | a0002c0002t0001g0017 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.233-110C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688785 | ||||||
chr2:97688786
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.233-109G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688786 | ||||||
chr2:97688792
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.233-103G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688792 | ||||||
chr2:97688857
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.233-38G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688857 | ||||||
chr2:97688878
|
T | G | 1 | a0002c0002t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-17T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688878 | ||||||
chr2:97688879
|
G | T | 1 | a0002c0002t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.233-16G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 3/7 | chr2 | 97688879 | ||||||
chr2:97689339
|
C | G | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.331+346C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689339 | ||||||
chr2:97689470
|
A | C | 26 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(23): Show | 30 | HG00597.hp2 HG01346.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.331+477A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689470 | ||||||
chr2:97689601
|
G | A | 3 | a0003c0003t0005g0095a0003c0003t0005g0096a0003c0003t0005g0234 | 3 | HG02040.hp2 HG03486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.331+608G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689601 | ||||||
chr2:97689758
|
G | A | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-498G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689758 | ||||||
chr2:97689950
|
G | A | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.332-306G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97689950 | ||||||
chr2:97690005
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.332-251C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690005 | ||||||
chr2:97690031
|
T | C | 4 | a0001c0001t0001g0089a0001c0001t0002g0005a0001c0001t0002g0212others(1): Show | 7 | HG01261.hp1 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.332-225T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690031 | ||||||
chr2:97690072
|
C | A | 39 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(36): Show | 44 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.332-184C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690072 | ||||||
chr2:97690145
|
C | A | 49 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0007others(46): Show | 75 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.332-111C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690145 | ||||||
chr2:97690147
|
A | G | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.332-109A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690147 | ||||||
chr2:97690157
|
C | A | 1 | a0003c0003t0003g0231 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.332-99C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690157 | ||||||
chr2:97690157
|
C | G | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.332-99C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 4/7 | chr2 | 97690157 | ||||||
chr2:97690454
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+127C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690454 | ||||||
chr2:97690537
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.403+210C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690537 | ||||||
chr2:97690563
|
A | G | 1 | a0002c0002t0001g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.403+236A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690563 | ||||||
chr2:97690571
|
C | T | 1 | a0002c0002t0001g0065 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.403+244C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690571 | ||||||
chr2:97690772
|
G | GT | 12 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(9): Show | 16 | HG01496.hp2 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.403+458dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97690772 | |||||
chr2:97690781
|
T | G | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.403+454T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690781 | ||||||
chr2:97690786
|
G | T | 1 | a0002c0002t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403+459G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690786 | ||||||
chr2:97690790
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+463T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690790 | ||||||
chr2:97690791
|
T | G | 6 | a0001c0001t0002g0190a0003c0003t0001g0038a0003c0003t0001g0039others(3): Show | 6 | HG00408.hp2 HG01346.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+464T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97690791 | ||||||
chr2:97691241
|
T | C | 1 | a0002c0002t0001g0007 | 3 | HG01123.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.403+914T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691241 | ||||||
chr2:97691249
|
C | T | 21 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(18): Show | 25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.403+922C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691249 | ||||||
chr2:97691360
|
C | T | 49 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0007others(46): Show | 75 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.403+1033C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691360 | ||||||
chr2:97691397
|
C | T | 1 | a0008c0009t0002g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403+1070C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691397 | ||||||
chr2:97691532
|
A | C | 1 | a0002c0002t0001g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.403+1205A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691532 | ||||||
chr2:97691620
|
C | A | 7 | a0003c0003t0004g0097a0003c0003t0004g0098a0003c0003t0004g0099others(4): Show | 7 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+1293C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691620 | ||||||
chr2:97691665
|
C | T | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.403+1338C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691665 | ||||||
chr2:97691831
|
C | T | 40 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(37): Show | 45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.403+1504C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97691831 | ||||||
chr2:97692025
|
T | C | 1 | a0004c0004t0001g0084 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.403+1698T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692025 | ||||||
chr2:97692203
|
T | C | 2 | a0001c0001t0002g0149a0001c0001t0002g0162 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.403+1876T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692203 | ||||||
chr2:97692323
|
G | C | 1 | a0001c0001t0002g0160 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.403+1996G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692323 | ||||||
chr2:97692407
|
C | CT | 21 | a0001c0001t0001g0093a0001c0001t0001g0133a0001c0001t0001g0139others(18): Show | 22 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.403+2100dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97692407 | |||||
chr2:97692407
|
CT | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 29 | HG01070.hp1 HG01243.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.403+2100delT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97692407 | |||||
chr2:97692701
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.403+2374T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692701 | ||||||
chr2:97692726
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.403+2399C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692726 | ||||||
chr2:97692943
|
A | C | 10 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(7): Show | 11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.403+2616A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97692943 | ||||||
chr2:97693002
|
G | A | 40 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(37): Show | 45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.403+2675G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693002 | ||||||
chr2:97693011
|
T | G | 1 | a0003c0003t0003g0231 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.403+2684T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693011 | ||||||
chr2:97693323
|
A | G | 13 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0112others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.403+2996A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693323 | ||||||
chr2:97693367
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.403+3040G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693367 | ||||||
chr2:97693419
|
C | T | 49 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0007others(46): Show | 75 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.403+3092C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97693419 | ||||||
chr2:97694036
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0158 | 3 | HG02055.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+3709A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694036 | ||||||
chr2:97694139
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(2): Show | 5 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+3812C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694139 | ||||||
chr2:97694214
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.403+3887G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694214 | ||||||
chr2:97694248
|
C | CT | 5 | a0002c0002t0001g0014a0002c0002t0001g0031a0002c0002t0001g0032others(2): Show | 6 | HG02109.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+3935dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694248 | |||||
chr2:97694284
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+3957G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694284 | ||||||
chr2:97694300
|
C | T | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.403+3973C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694300 | ||||||
chr2:97694302
|
C | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 52 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(49): Show |
intron_variant | MODIFIER | c.403+3975C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694302 | ||||||
chr2:97694409
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0138 | 3 | HG01261.hp2 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.403+4082C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694409 | ||||||
chr2:97694415
|
A | AT | 27 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 32 | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.403+4106dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | |||||
chr2:97694415
|
A | ATTT | 19 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(16): Show | 24 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.403+4104_403+4106d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | |||||
chr2:97694415
|
A | ATTTT | 8 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0225others(5): Show | 8 | HG01346.hp1 HG01361.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+4103_403+4106d others(6): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | |||||
chr2:97694415
|
ATTT | A | 7 | a0003c0003t0004g0097a0003c0003t0004g0098a0003c0003t0004g0099others(4): Show | 7 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+4104_403+4106d others(5): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97694415 | |||||
chr2:97694583
|
C | T | 7 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(4): Show | 7 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+4256C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694583 | ||||||
chr2:97694802
|
A | C | 147 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(144): Show | 191 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.404-4224A>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694802 | ||||||
chr2:97694803
|
C | G | 1 | a0004c0004t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.404-4223C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97694803 | ||||||
chr2:97695088
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.404-3938T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97695088 | ||||||
chr2:97695141
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.404-3885C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97695141 | ||||||
chr2:97695493
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.404-3533C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97695493 | ||||||
chr2:97695736
|
C | CTTTCT | 5 | a0002c0002t0001g0072a0002c0005t0001g0035a0002c0005t0001g0036others(2): Show | 5 | HG00621.hp2 HG03486.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-3266_404-3262d others(7): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | |||||
chr2:97695736
|
C | CTTTCTTT others(3): Show |
12 | a0003c0003t0005g0095a0003c0003t0005g0234a0004c0004t0001g0018others(9): Show | 13 | HG01358.hp1 HG02040.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.404-3271_404-3262d others(12): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | |||||
chr2:97695736
|
C | CTTTCTTT others(8): Show |
2 | a0004c0004t0001g0084a0004c0004t0001g0092 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.404-3276_404-3262d others(17): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | |||||
chr2:97695736
|
C | CTTTCTTT others(23): Show |
1 | a0006c0010t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.404-3262_404-3261i others(32): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97695736 | |||||
chr2:97696007
|
C | A | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.404-3019C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696007 | ||||||
chr2:97696054
|
T | G | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.404-2972T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696054 | ||||||
chr2:97696199
|
A | G | 1 | a0003c0003t0005g0095 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.404-2827A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696199 | ||||||
chr2:97696436
|
C | CA | 23 | a0001c0001t0002g0167a0001c0001t0002g0177a0003c0003t0003g0006others(20): Show | 27 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.404-2580dupA | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97696436 | |||||
chr2:97696445
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0134 | 2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.404-2581A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696445 | ||||||
chr2:97696534
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 5 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-2492G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696534 | ||||||
chr2:97696667
|
T | C | 40 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(37): Show | 45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.404-2359T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696667 | ||||||
chr2:97696693
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.404-2333G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696693 | ||||||
chr2:97696778
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.404-2248C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696778 | ||||||
chr2:97696873
|
T | C | 1 | a0002c0002t0001g0015 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.404-2153T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97696873 | ||||||
chr2:97697239
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-1787C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697239 | ||||||
chr2:97697295
|
G | A | 1 | a0003c0003t0004g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.404-1731G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697295 | ||||||
chr2:97697351
|
A | G | 4 | a0002c0002t0001g0014a0002c0002t0001g0031a0002c0002t0001g0032others(1): Show | 5 | HG02109.hp2 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-1675A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697351 | ||||||
chr2:97697454
|
G | A | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.404-1572G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697454 | ||||||
chr2:97697982
|
C | T | 5 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0005g0095others(2): Show | 5 | HG01346.hp1 HG01361.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-1044C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97697982 | ||||||
chr2:97697984
|
CTG | C | 5 | a0001c0001t0002g0011a0001c0001t0002g0159a0001c0001t0002g0163others(2): Show | 7 | HG00741.hp1 HG01070.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-1039_404-1038d others(4): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 97697984 | |||||
chr2:97698000
|
G | C | 5 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0005g0095others(2): Show | 5 | HG01346.hp1 HG01361.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-1026G>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698000 | ||||||
chr2:97698059
|
T | G | 21 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(18): Show | 25 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.404-967T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698059 | ||||||
chr2:97698176
|
C | A | 3 | a0001c0001t0002g0167a0001c0001t0002g0178a0001c0001t0002g0185 | 3 | NA18952.hp2 NA18961.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.404-850C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698176 | ||||||
chr2:97698446
|
T | C | 147 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(144): Show | 191 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.404-580T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698446 | ||||||
chr2:97698514
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.404-512G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698514 | ||||||
chr2:97698566
|
A | G | 2 | a0004c0004t0001g0091a0004c0004t0001g0092 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-460A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698566 | ||||||
chr2:97698708
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.404-318T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 5/7 | chr2 | 97698708 | ||||||
chr2:97699345
|
C | T | 1 | a0006c0010t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.514+209C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699345 | ||||||
chr2:97699495
|
G | A | 27 | a0001c0001t0002g0164a0001c0001t0002g0175a0001c0001t0002g0179others(24): Show | 31 | HG00597.hp2 HG01106.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.514+359G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699495 | ||||||
chr2:97699515
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.514+379G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699515 | ||||||
chr2:97699612
|
T | A | 2 | a0001c0001t0002g0168a0003c0003t0003g0229 | 2 | HG01993.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.514+476T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699612 | ||||||
chr2:97699933
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.514+797C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97699933 | ||||||
chr2:97700028
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0002g0175 | 2 | HG01106.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.514+892G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700028 | ||||||
chr2:97700331
|
G | A | 2 | a0001c0001t0002g0187a0001c0001t0002g0189 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.515-823G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700331 | ||||||
chr2:97700609
|
C | G | 2 | a0001c0001t0001g0126a0001c0001t0002g0207 | 2 | NA18906.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.515-545C>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700609 | ||||||
chr2:97700629
|
C | T | 1 | a0002c0002t0001g0044 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.515-525C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700629 | ||||||
chr2:97700729
|
TG | T | 19 | a0003c0003t0003g0006a0003c0003t0003g0012a0003c0003t0003g0223others(16): Show | 23 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.515-424delG | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700729 | ||||||
chr2:97700730
|
G | GT | 51 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0004others(48): Show | 84 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.515-413dupT | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 97700730 | |||||
chr2:97700730
|
G | T | 2 | a0003c0003t0003g0225a0003c0003t0004g0101 | 2 | HG04115.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.515-424G>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700730 | ||||||
chr2:97700787
|
G | A | 14 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(11): Show | 15 | HG01243.hp1 HG01358.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.515-367G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700787 | ||||||
chr2:97700791
|
T | G | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.515-363T>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700791 | ||||||
chr2:97700800
|
G | A | 10 | a0004c0004t0001g0018a0004c0004t0001g0080a0004c0004t0001g0081others(7): Show | 11 | HG01358.hp1 HG02451.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.515-354G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700800 | ||||||
chr2:97700891
|
G | A | 3 | a0001c0001t0002g0165a0001c0001t0002g0192a0001c0001t0002g0194 | 3 | HG02055.hp1 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.515-263G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700891 | ||||||
chr2:97700953
|
G | A | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.515-201G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700953 | ||||||
chr2:97700977
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.515-177C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700977 | ||||||
chr2:97700983
|
A | G | 40 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(37): Show | 45 | HG00597.hp2 HG01243.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.515-171A>G | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97700983 | ||||||
chr2:97701027
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0158 | 3 | HG02055.hp2 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.515-127G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 6/7 | chr2 | 97701027 | ||||||
chr2:97701308
|
C | A | 147 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(144): Show | 191 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(188): Show |
splice_region_variant&intron_variant | LOW | c.665+4C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701308 | ||||||
chr2:97701483
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.665+179G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701483 | ||||||
chr2:97701494
|
G | A | 1 | a0007c0008t0002g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665+190G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701494 | ||||||
chr2:97701503
|
G | A | 1 | a0004c0004t0001g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.665+199G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701503 | ||||||
chr2:97701514
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.665+210G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701514 | ||||||
chr2:97701736
|
T | C | 235 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0019others(232): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.665+432T>C | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701736 | ||||||
chr2:97701888
|
T | A | 1 | a0001c0001t0002g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.665+584T>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97701888 | ||||||
chr2:97701888
|
TGTCTACA others(5): Show |
T | 1 | a0001c0001t0001g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.665+594_665+605del others(12): Show |
C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 97701888 | |||||
chr2:97702181
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(43): Show | 51 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.666-488G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702181 | ||||||
chr2:97702572
|
C | A | 1 | a0002c0002t0001g0047 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.666-97C>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702572 | ||||||
chr2:97702572
|
C | T | 26 | a0003c0003t0001g0038a0003c0003t0001g0039a0003c0003t0003g0006others(23): Show | 30 | HG00597.hp2 HG01346.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.666-97C>T | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702572 | ||||||
chr2:97702618
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(3): Show | 10 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.666-51G>A | C2orf92 | ENSG00000228486.11 | transcript | ENST00000627399.4 | protein_coding | 7/7 | chr2 | 97702618 |