geneid | 9648 |
---|---|
ensemblid | ENSG00000135968.22 |
hgncid | 23218 |
symbol | GCC2 |
name | GRIP and coiled-coil domain containing 2 |
refseq_nuc | NM_181453.4 |
refseq_prot | NP_852118.2 |
ensembl_nuc | ENST00000309863.11 |
ensembl_prot | ENSP00000307939.5 |
mane_status | MANE Select |
chr | chr2 |
start | 108449206 |
end | 108509415 |
strand | + |
ver | v1.2 |
region | chr2:108449206-108509415 |
region5000 | chr2:108444206-108514415 |
regionname0 | GCC2_chr2_108449206_108509415 |
regionname5000 | GCC2_chr2_108444206_108514415 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1684 | 252 | 75 | 47 | 71 | 16 | 42 | 64 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0002 | 0/0 | 1684 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0003 | 0/0 | 1684 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0004 | 0/0 | 1684 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0005 | 0/0 | 1684 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0006 | 1/0 | 1684 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0007 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0008 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0009 | 0/0 | 1684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0010 | 0/0 | 1684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 5055 | 150 | 57 | 27 | 26 | 10 | 30 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0002 | 0/1 | 5055 | 84 | 12 | 13 | 41 | 6 | 11 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0003 | 0/0 | 5055 | 7 | 0 | 0 | 7 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0004 | 0/0 | 5055 | 7 | 7 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0005 | 0/0 | 5055 | 5 | 0 | 5 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0006 | 0/0 | 5055 | 4 | 4 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0007 | 0/0 | 5055 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0008 | 0/0 | 5055 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0009 | 0/0 | 5055 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0010 | 0/0 | 5055 | 2 | 1 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0011 | 1/0 | 5055 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0012 | 0/0 | 5055 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0013 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0014 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0015 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0016 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0017 | 0/0 | 5055 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0018 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
c0019 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1853 | 74 | 5 | 15 | 42 | 4 | 8 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0002 | 0/0 | 1856 | 41 | 11 | 7 | 13 | 2 | 8 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0003 | 0/0 | 1856 | 33 | 5 | 6 | 9 | 2 | 11 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0004 | 0/0 | 1856 | 14 | 1 | 6 | 0 | 2 | 5 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0005 | 0/0 | 1856 | 10 | 8 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0006 | 0/0 | 1856 | 9 | 0 | 1 | 6 | 0 | 2 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0007 | 0/0 | 1856 | 7 | 7 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0008 | 0/1 | 1858 | 7 | 0 | 2 | 0 | 2 | 2 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0009 | 0/0 | 1856 | 6 | 5 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0010 | 0/0 | 1856 | 6 | 5 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0011 | 0/0 | 1856 | 5 | 4 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0012 | 0/0 | 1856 | 4 | 4 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0013 | 0/0 | 1851 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0014 | 0/0 | 1856 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0015 | 0/0 | 1856 | 3 | 0 | 3 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0016 | 0/0 | 1856 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0017 | 0/0 | 1856 | 3 | 0 | 0 | 0 | 0 | 3 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0018 | 0/0 | 1856 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0019 | 0/0 | 1856 | 2 | 1 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0020 | 0/0 | 1853 | 2 | 1 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0021 | 0/0 | 1853 | 2 | 1 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0022 | 0/0 | 1856 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0023 | 0/0 | 1851 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0024 | 0/0 | 1856 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0025 | 0/0 | 1858 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0026 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0027 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0028 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0029 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0030 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0031 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0032 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0033 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0034 | 0/0 | 1853 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0035 | 0/0 | 1853 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0036 | 0/0 | 1858 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0037 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0038 | 0/0 | 1858 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0039 | 0/0 | 1856 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0040 | 0/0 | 1856 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0041 | 1/0 | 1855 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0042 | 0/0 | 1856 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0043 | 0/0 | 1856 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0044 | 0/0 | 1856 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0045 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0046 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0047 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0048 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0049 | 0/0 | 1856 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0050 | 0/0 | 1856 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0051 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0052 | 0/0 | 1851 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
t0053 | 0/0 | 1858 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5055 | 150 | 57 | 27 | 26 | 10 | 30 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002 | 0/1 | 5055 | 84 | 12 | 13 | 41 | 6 | 11 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0005 | 0/0 | 5055 | 5 | 0 | 5 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0006 | 0/0 | 5055 | 4 | 4 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0008 | 0/0 | 5055 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0009 | 0/0 | 5055 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0012 | 0/0 | 5055 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0013 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0015 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0019 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0002c0003 | 0/0 | 5055 | 7 | 0 | 0 | 7 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0003c0004 | 0/0 | 5055 | 7 | 7 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0004c0007 | 0/0 | 5055 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0005c0010 | 0/0 | 5055 | 2 | 1 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0006c0011 | 1/0 | 5055 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0007c0014 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0008c0016 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0009c0017 | 0/0 | 5055 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0010c0018 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6910 | 39 | 10 | 7 | 13 | 2 | 7 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0003 | 0/0 | 6910 | 24 | 5 | 4 | 2 | 2 | 11 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0004 | 0/0 | 6910 | 14 | 1 | 6 | 0 | 2 | 5 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0005 | 0/0 | 6910 | 10 | 8 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0006 | 0/0 | 6910 | 9 | 0 | 1 | 6 | 0 | 2 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0007 | 0/0 | 6910 | 7 | 7 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0009 | 0/0 | 6910 | 5 | 4 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0010 | 0/0 | 6910 | 5 | 4 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0011 | 0/0 | 6910 | 5 | 4 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0015 | 0/0 | 6910 | 3 | 0 | 3 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0016 | 0/0 | 6910 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0017 | 0/0 | 6910 | 3 | 0 | 0 | 0 | 0 | 3 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0019 | 0/0 | 6910 | 2 | 1 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0024 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0025 | 0/0 | 6912 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0026 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0027 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0028 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0029 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0033 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0036 | 0/0 | 6912 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0037 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0038 | 0/0 | 6912 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0039 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0040 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0042 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0043 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0044 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0045 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0048 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0049 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0001t0053 | 0/0 | 6912 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0001 | 0/0 | 6907 | 67 | 5 | 10 | 40 | 4 | 8 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0008 | 0/1 | 6912 | 7 | 0 | 2 | 0 | 2 | 2 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0013 | 0/0 | 6905 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0021 | 0/0 | 6907 | 2 | 1 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0023 | 0/0 | 6905 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0034 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0035 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0002t0052 | 0/0 | 6905 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0005t0001 | 0/0 | 6907 | 5 | 0 | 5 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0006t0018 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0006t0032 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0008t0014 | 0/0 | 6910 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0009t0003 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0012t0002 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0013t0046 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0015t0001 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0001c0019t0010 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0002c0003t0003 | 0/0 | 6910 | 7 | 0 | 0 | 7 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0003c0004t0012 | 0/0 | 6910 | 4 | 4 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0003c0004t0030 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0003c0004t0031 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0003c0004t0051 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0004c0007t0022 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0004c0007t0047 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0005c0010t0020 | 0/0 | 6907 | 2 | 1 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0006c0011t0041 | 1/0 | 6909 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0007c0014t0009 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0008c0016t0002 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0009c0017t0050 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
a0010c0018t0001 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | copy fasta | chr2 | 108444206 | 108514415 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0009g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0010g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0015g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0015g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0015g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0016g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0016g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0016g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0017g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0017g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0017g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0019g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0019g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0024g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0024g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0025g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0025g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0026g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0027g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0028g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0029g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0033g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0036g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0037g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0038g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0039g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0040g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0042g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0043g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0044g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0045g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0048g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0049g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0001t0053g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0008g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0021g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0021g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0023g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0023g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0034g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0035g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0002t0052g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0005t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0005t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0006t0018g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0006t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0006t0018g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0006t0032g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0008t0014g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0008t0014g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0008t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0009t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0012t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0013t0046g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0015t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0001c0019t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0002c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0030g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0031g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0003c0004t0051g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0004c0007t0022g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0004c0007t0022g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0004c0007t0047g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0005c0010t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0005c0010t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0006c0011t0041g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0007c0014t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0008c0016t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0009c0017t0050g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
a0010c0018t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0068 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0105 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00323 | hp2 | a0001 | c0002 | t0008 | g0021 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00639 | hp2 | a0001 | c0002 | t0008 | g0018 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00642 | hp1 | a0001 | c0001 | t0015 | g0244 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00642 | hp2 | a0001 | c0001 | t0053 | g0174 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00673 | hp1 | a0001 | c0015 | t0001 | g0069 | EAS | CHS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0093 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0249 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01167 | hp1 | a0001 | c0005 | t0001 | g0029 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01175 | hp1 | a0001 | c0001 | t0009 | g0219 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0245 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01192 | hp1 | a0001 | c0002 | t0034 | g0073 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0139 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01256 | hp1 | a0001 | c0002 | t0008 | g0017 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01257 | hp1 | a0001 | c0001 | t0015 | g0242 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01257 | hp2 | a0001 | c0009 | t0003 | g0005 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01258 | hp1 | a0001 | c0009 | t0003 | g0005 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0239 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01261 | hp1 | a0009 | c0017 | t0050 | g0163 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01261 | hp2 | a0001 | c0001 | t0043 | g0243 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01361 | hp2 | a0001 | c0005 | t0001 | g0053 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01515 | hp1 | a0001 | c0001 | t0042 | g0250 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01515 | hp2 | a0001 | c0001 | t0044 | g0235 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01516 | hp1 | a0001 | c0001 | t0040 | g0173 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01516 | hp2 | a0001 | c0001 | t0038 | g0247 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01884 | hp1 | a0001 | c0001 | t0025 | g0095 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0262 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01928 | hp2 | a0001 | c0005 | t0001 | g0052 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01981 | hp1 | a0001 | c0005 | t0001 | g0034 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02040 | hp2 | a0005 | c0010 | t0020 | g0159 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02055 | hp2 | a0001 | c0001 | t0024 | g0257 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02148 | hp1 | a0001 | c0005 | t0001 | g0051 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02257 | hp1 | a0001 | c0001 | t0029 | g0217 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02257 | hp2 | a0001 | c0001 | t0033 | g0261 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02258 | hp2 | a0003 | c0004 | t0012 | g0167 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02280 | hp1 | a0001 | c0001 | t0026 | g0007 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0265 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02572 | hp2 | a0001 | c0001 | t0045 | g0153 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02622 | hp1 | a0001 | c0001 | t0048 | g0144 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02630 | hp2 | a0001 | c0006 | t0032 | g0147 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02647 | hp1 | a0004 | c0007 | t0022 | g0234 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02647 | hp2 | a0001 | c0006 | t0018 | g0149 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02698 | hp2 | a0001 | c0001 | t0019 | g0164 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0198 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0251 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0236 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0183 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02886 | hp1 | a0001 | c0001 | t0011 | g0151 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02895 | hp1 | a0001 | c0002 | t0023 | g0157 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02897 | hp1 | a0001 | c0002 | t0023 | g0155 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02922 | hp1 | a0003 | c0004 | t0012 | g0170 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02965 | hp1 | a0008 | c0016 | t0002 | g0188 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02976 | hp1 | a0001 | c0001 | t0025 | g0100 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03041 | hp1 | a0001 | c0002 | t0052 | g0156 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03041 | hp2 | a0001 | c0001 | t0036 | g0115 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0267 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0263 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03130 | hp2 | a0001 | c0001 | t0024 | g0266 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03195 | hp1 | a0001 | c0006 | t0018 | g0146 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03195 | hp2 | a0003 | c0004 | t0012 | g0168 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0130 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03225 | hp1 | a0001 | c0001 | t0027 | g0216 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03225 | hp2 | a0003 | c0004 | t0051 | g0169 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0237 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03453 | hp1 | a0003 | c0004 | t0012 | g0171 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03453 | hp2 | a0001 | c0019 | t0010 | g0154 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03486 | hp1 | a0003 | c0004 | t0031 | g0172 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03486 | hp2 | a0004 | c0007 | t0022 | g0233 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03491 | hp2 | a0001 | c0001 | t0017 | g0097 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03492 | hp2 | a0001 | c0001 | t0017 | g0098 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03516 | hp1 | a0001 | c0001 | t0037 | g0134 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03704 | hp1 | a0001 | c0001 | t0006 | g0213 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03710 | hp1 | a0001 | c0002 | t0008 | g0085 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03927 | hp1 | a0001 | c0002 | t0021 | g0087 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04184 | hp1 | a0001 | c0001 | t0017 | g0126 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04228 | hp1 | a0001 | c0002 | t0008 | g0020 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG04228 | hp2 | a0001 | c0012 | t0002 | g0203 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18522 | hp1 | a0007 | c0014 | t0009 | g0218 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | CHB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | CHB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18940 | hp2 | a0001 | c0001 | t0049 | g0122 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18947 | hp1 | a0002 | c0003 | t0003 | g0107 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18947 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18954 | hp2 | a0001 | c0008 | t0014 | g0161 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18960 | hp1 | a0002 | c0003 | t0003 | g0110 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18969 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18970 | hp2 | a0001 | c0008 | t0014 | g0162 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18989 | hp2 | a0001 | c0002 | t0035 | g0082 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18994 | hp1 | a0001 | c0001 | t0016 | g0121 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18997 | hp2 | a0010 | c0018 | t0001 | g0063 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19030 | hp1 | a0001 | c0001 | t0028 | g0209 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19030 | hp2 | a0004 | c0007 | t0047 | g0253 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19043 | hp1 | a0001 | c0002 | t0013 | g0090 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19043 | hp2 | a0005 | c0010 | t0020 | g0158 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19056 | hp1 | a0001 | c0001 | t0016 | g0113 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19062 | hp2 | a0002 | c0003 | t0003 | g0111 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19066 | hp2 | a0002 | c0003 | t0003 | g0112 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19067 | hp1 | a0002 | c0003 | t0003 | g0106 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19074 | hp1 | a0002 | c0003 | t0003 | g0108 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19080 | hp2 | a0002 | c0003 | t0003 | g0109 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19081 | hp2 | a0001 | c0001 | t0016 | g0124 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19083 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19088 | hp2 | a0001 | c0008 | t0014 | g0160 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19089 | hp1 | a0001 | c0001 | t0039 | g0137 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20129 | hp1 | a0001 | c0002 | t0021 | g0002 | AFR | ASW | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20129 | hp2 | a0001 | c0002 | t0013 | g0089 | AFR | ASW | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20752 | hp2 | a0001 | c0002 | t0008 | g0084 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | GIH | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | GIH | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02486 | hp2 | a0001 | c0006 | t0018 | g0148 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG02559 | hp2 | a0001 | c0002 | t0013 | g0088 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03471 | hp1 | a0003 | c0004 | t0030 | g0166 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG06807 | hp1 | a0001 | c0013 | t0046 | g0177 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0260 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20300 | hp1 | a0001 | c0001 | t0010 | g0264 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA21309 | hp1 | a0001 | c0001 | t0019 | g0202 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0008 | g0019 | REF | REF | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
homoSapiens_grch38 | hp1 | a0006 | c0011 | t0041 | g0165 | REF | REF | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108452435
|
C | G | 1 | a0003 | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
missense_variant | MODERATE | c.185C>G | p.Pro62Arg | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/23 | 254/6909 | 185/5055 | 62/1684 | chr2 | 108452435 | ||
chr2:108470281
|
A | G | 1 | a0010 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.952A>G | p.Ile318Val | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1021/6909 | 952/5055 | 318/1684 | chr2 | 108470281 | ||
chr2:108470716
|
A | C | 1 | a0009 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.1387A>C | p.Lys463Gln | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1456/6909 | 1387/5055 | 463/1684 | chr2 | 108470716 | ||
chr2:108470867
|
C | T | 1 | a0008 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.1538C>T | p.Ala513Val | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1607/6909 | 1538/5055 | 513/1684 | chr2 | 108470867 | ||
chr2:108471107
|
C | G | 1 | a0005 | 2 | HG02040.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1778C>G | p.Thr593Ser | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1847/6909 | 1778/5055 | 593/1684 | chr2 | 108471107 | ||
chr2:108471875
|
A | G | 1 | a0007 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2546A>G | p.Glu849Gly | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 2615/6909 | 2546/5055 | 849/1684 | chr2 | 108471875 | ||
chr2:108482398
|
A | G | 1 | a0002 | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
missense_variant | MODERATE | c.3292A>G | p.Met1098Val | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/23 | 3361/6909 | 3292/5055 | 1098/1684 | chr2 | 108482398 | ||
chr2:108483075
|
C | G | 1 | a0004 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.3359C>G | p.Thr1120Ser | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/23 | 3428/6909 | 3359/5055 | 1120/1684 | chr2 | 108483075 | ||
chr2:108483116
|
C | G | 9 | a0001a0002a0003others(6): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
missense_variant | MODERATE | c.3400C>G | p.Gln1134Glu | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/23 | 3469/6909 | 3400/5055 | 1134/1684 | chr2 | 108483116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108470109
|
A | G | 1 | a0001c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.780A>G | p.Glu260Glu | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 849/6909 | 780/5055 | 260/1684 | chr2 | 108470109 | ||
chr2:108470358
|
A | G | 2 | a0001c0008a0009c0017 | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
synonymous_variant | LOW | c.1029A>G | p.Glu343Glu | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1098/6909 | 1029/5055 | 343/1684 | chr2 | 108470358 | ||
chr2:108471240
|
C | T | 1 | a0001c0006 | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.1911C>T | p.Tyr637Tyr | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1980/6909 | 1911/5055 | 637/1684 | chr2 | 108471240 | ||
chr2:108471471
|
A | G | 1 | a0001c0015 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.2142A>G | p.Gln714Gln | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 2211/6909 | 2142/5055 | 714/1684 | chr2 | 108471471 | ||
chr2:108471819
|
G | A | 1 | a0001c0005 | 5 | HG01167.hp1 HG01361.hp2 HG01928.hp2 others(2): Show |
synonymous_variant | LOW | c.2490G>A | p.Lys830Lys | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 2559/6909 | 2490/5055 | 830/1684 | chr2 | 108471819 | ||
chr2:108489925
|
A | G | 5 | a0001c0002a0001c0005a0001c0015others(2): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
synonymous_variant | LOW | c.4140A>G | p.Gln1380Gln | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/23 | 4209/6909 | 4140/5055 | 1380/1684 | chr2 | 108489925 | ||
chr2:108492627
|
T | A | 1 | a0001c0012 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.4284T>A | p.Thr1428Thr | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/23 | 4353/6909 | 4284/5055 | 1428/1684 | chr2 | 108492627 | ||
chr2:108492780
|
G | T | 1 | a0003c0004 | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.4437G>T | p.Pro1479Pro | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/23 | 4506/6909 | 4437/5055 | 1479/1684 | chr2 | 108492780 | ||
chr2:108495412
|
G | A | 1 | a0001c0009 | 2 | HG01257.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.4569G>A | p.Thr1523Thr | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/23 | 4638/6909 | 4569/5055 | 1523/1684 | chr2 | 108495412 | ||
chr2:108497028
|
C | T | 1 | a0001c0013 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.4701C>T | p.Ser1567Ser | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/23 | 4770/6909 | 4701/5055 | 1567/1684 | chr2 | 108497028 | ||
chr2:108499744
|
G | A | 1 | a0005c0010 | 2 | HG02040.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.4974G>A | p.Ala1658Ala | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/23 | 5043/6909 | 4974/5055 | 1658/1684 | chr2 | 108499744 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108507786
|
T | A | 11 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(8): Show | 62 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*156T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 156 | chr2 | 108507786 | |||||
chr2:108507816
|
G | A | 1 | a0001c0001t0026 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 186 | chr2 | 108507816 | |||||
chr2:108507823
|
G | C | 13 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(10): Show | 64 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*193G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 193 | chr2 | 108507823 | |||||
chr2:108507852
|
T | C | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0033others(4): Show | 22 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*222T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 222 | chr2 | 108507852 | |||||
chr2:108507900
|
C | A | 10 | a0001c0002t0001a0001c0002t0008a0001c0002t0013others(7): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 270 | chr2 | 108507900 | |||||
chr2:108507919
|
G | A | 3 | a0001c0001t0011a0001c0001t0036a0001c0001t0037 | 7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*289G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 289 | chr2 | 108507919 | |||||
chr2:108508056
|
T | G | 1 | a0001c0001t0038 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 426 | chr2 | 108508056 | |||||
chr2:108508066
|
A | C | 2 | a0001c0001t0038a0003c0004t0031 | 2 | HG01516.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*436A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 436 | chr2 | 108508066 | |||||
chr2:108508068
|
G | C | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 438 | chr2 | 108508068 | |||||
chr2:108508069
|
C | G | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 439 | chr2 | 108508069 | |||||
chr2:108508078
|
T | C | 9 | a0001c0001t0036a0001c0002t0001a0001c0002t0008others(6): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 448 | chr2 | 108508078 | |||||
chr2:108508080
|
C | T | 8 | a0001c0002t0001a0001c0002t0008a0001c0002t0021others(5): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 450 | chr2 | 108508080 | |||||
chr2:108508100
|
A | ATT | 13 | a0001c0001t0025a0001c0001t0036a0001c0001t0038others(10): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*470_*471insTT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 471 | chr2 | 108508100 | |||||
chr2:108508101
|
C | G | 13 | a0001c0001t0025a0001c0001t0036a0001c0001t0038others(10): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*471C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 471 | chr2 | 108508101 | |||||
chr2:108508103
|
C | A | 13 | a0001c0001t0025a0001c0001t0036a0001c0001t0038others(10): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*473C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 473 | chr2 | 108508103 | |||||
chr2:108508157
|
G | A | 2 | a0001c0001t0038a0001c0001t0053 | 2 | HG00642.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*527G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 527 | chr2 | 108508157 | |||||
chr2:108508160
|
A | G | 2 | a0001c0001t0038a0001c0001t0053 | 2 | HG00642.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*530A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 530 | chr2 | 108508160 | |||||
chr2:108508176
|
G | A | 1 | a0001c0001t0038 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 546 | chr2 | 108508176 | |||||
chr2:108508205
|
G | T | 2 | a0001c0001t0038a0001c0001t0053 | 2 | HG00642.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 575 | chr2 | 108508205 | |||||
chr2:108508207
|
T | C | 1 | a0001c0001t0040 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 577 | chr2 | 108508207 | |||||
chr2:108508267
|
G | A | 1 | a0001c0001t0038 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 637 | chr2 | 108508267 | |||||
chr2:108508321
|
A | G | 35 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(32): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*691A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 691 | chr2 | 108508321 | |||||
chr2:108508381
|
A | T | 1 | a0001c0001t0044 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 751 | chr2 | 108508381 | |||||
chr2:108508392
|
T | C | 2 | a0001c0001t0019a0001c0001t0027 | 3 | HG02698.hp2 HG03225.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*762T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 762 | chr2 | 108508392 | |||||
chr2:108508447
|
A | C | 2 | a0001c0002t0023a0001c0002t0052 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*817A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 817 | chr2 | 108508447 | |||||
chr2:108508451
|
G | A | 1 | a0001c0001t0024 | 2 | HG02055.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 821 | chr2 | 108508451 | |||||
chr2:108508463
|
A | AC | 49 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(46): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*834dupC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 835 | INFO_REALIGN_3_PRIME | chr2 | 108508463 | ||||
chr2:108508464
|
CACTT | C | 12 | a0001c0002t0001a0001c0002t0008a0001c0002t0013others(9): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*835_*838delACTT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 835 | chr2 | 108508464 | |||||
chr2:108508469
|
G | C | 12 | a0001c0002t0001a0001c0002t0008a0001c0002t0013others(9): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*839G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 839 | chr2 | 108508469 | |||||
chr2:108508471
|
G | C | 12 | a0001c0002t0001a0001c0002t0008a0001c0002t0013others(9): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 841 | chr2 | 108508471 | |||||
chr2:108508519
|
T | TGCATG | 1 | a0001c0002t0008 | 7 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*890_*894dupGCATG | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 895 | INFO_REALIGN_3_PRIME | chr2 | 108508519 | ||||
chr2:108508526
|
A | G | 4 | a0003c0004t0012a0003c0004t0030a0003c0004t0031others(1): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*896A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 896 | chr2 | 108508526 | |||||
chr2:108508580
|
A | C | 9 | a0001c0001t0017a0001c0001t0033a0001c0001t0038others(6): Show | 14 | HG01261.hp1 HG01261.hp2 HG01516.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*950A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 950 | chr2 | 108508580 | |||||
chr2:108508662
|
G | C | 1 | a0001c0002t0034 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1032 | chr2 | 108508662 | |||||
chr2:108508708
|
A | G | 12 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(9): Show | 60 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1078 | chr2 | 108508708 | |||||
chr2:108508711
|
G | T | 6 | a0001c0001t0015a0001c0001t0027a0001c0001t0044others(3): Show | 10 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1081G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1081 | chr2 | 108508711 | |||||
chr2:108508724
|
C | T | 5 | a0001c0001t0015a0001c0001t0027a0001c0001t0029others(2): Show | 8 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1094 | chr2 | 108508724 | |||||
chr2:108508764
|
T | G | 2 | a0001c0001t0048a0004c0007t0022 | 3 | HG02622.hp1 HG02647.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1134T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1134 | chr2 | 108508764 | |||||
chr2:108508765
|
C | G | 5 | a0001c0001t0016a0001c0001t0042a0001c0001t0049others(2): Show | 13 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1135C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1135 | chr2 | 108508765 | |||||
chr2:108508799
|
T | G | 2 | a0003c0004t0030a0003c0004t0031 | 2 | HG03471.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1169T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1169 | chr2 | 108508799 | |||||
chr2:108508813
|
A | G | 1 | a0001c0013t0046 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1183 | chr2 | 108508813 | |||||
chr2:108508857
|
G | A | 1 | a0001c0002t0035 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1227G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1227 | chr2 | 108508857 | |||||
chr2:108509026
|
A | T | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1396A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1396 | chr2 | 108509026 | |||||
chr2:108509050
|
A | C | 1 | a0001c0002t0052 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1420 | chr2 | 108509050 | |||||
chr2:108509117
|
T | C | 1 | a0001c0002t0052 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1487T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1487 | chr2 | 108509117 | |||||
chr2:108509164
|
A | G | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1534A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1534 | chr2 | 108509164 | |||||
chr2:108509206
|
T | C | 2 | a0001c0006t0018a0001c0006t0032 | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1576T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1576 | chr2 | 108509206 | |||||
chr2:108509230
|
T | C | 1 | a0003c0004t0051 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1600 | chr2 | 108509230 | |||||
chr2:108509322
|
A | G | 1 | a0001c0001t0045 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1692 | chr2 | 108509322 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108449402
|
T | C | 162 | a0001c0001t0002g0152a0001c0001t0003g0004a0001c0001t0003g0096others(159): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.6+122T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449402 | ||||||
chr2:108449434
|
C | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+154C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449434 | ||||||
chr2:108449463
|
T | C | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.7-170T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449463 | ||||||
chr2:108449492
|
CCGTCCGC others(7): Show |
C | 1 | a0001c0001t0004g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7-139_7-126delGTCC others(10): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 108449492 | |||||
chr2:108449517
|
C | A | 1 | a0001c0001t0019g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7-116C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449517 | ||||||
chr2:108449554
|
C | T | 1 | a0001c0001t0004g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7-79C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449554 | ||||||
chr2:108449598
|
T | A | 1 | a0001c0001t0004g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7-35T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449598 | ||||||
chr2:108449722
|
A | G | 1 | a0001c0001t0004g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+33A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449722 | ||||||
chr2:108449778
|
AT | A | 68 | a0001c0001t0002g0152a0001c0001t0003g0004a0001c0001t0003g0096others(65): Show | 70 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.63+102delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 108449778 | |||||
chr2:108449792
|
A | T | 1 | a0001c0001t0004g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+103A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449792 | ||||||
chr2:108449798
|
C | T | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+109C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449798 | ||||||
chr2:108449810
|
G | T | 2 | a0001c0002t0001g0091a0001c0002t0001g0092 | 2 | HG01123.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+121G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449810 | ||||||
chr2:108449832
|
A | G | 269 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.63+143A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449832 | ||||||
chr2:108449855
|
C | T | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+166C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449855 | ||||||
chr2:108449874
|
AAG | A | 16 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(13): Show | 17 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+187_63+188delGA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 108449874 | |||||
chr2:108449888
|
G | A | 168 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+199G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449888 | ||||||
chr2:108449968
|
G | A | 84 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.63+279G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449968 | ||||||
chr2:108450003
|
C | A | 1 | a0003c0004t0030g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+314C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450003 | ||||||
chr2:108450030
|
T | C | 1 | a0001c0001t0040g0173 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.63+341T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450030 | ||||||
chr2:108450076
|
T | C | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+387T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450076 | ||||||
chr2:108450115
|
T | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+426T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450115 | ||||||
chr2:108450132
|
T | C | 1 | a0001c0001t0053g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.63+443T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450132 | ||||||
chr2:108450196
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+507A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450196 | ||||||
chr2:108450237
|
G | C | 1 | a0001c0002t0001g0011 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.63+548G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450237 | ||||||
chr2:108450340
|
T | C | 1 | a0001c0001t0006g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.63+651T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450340 | ||||||
chr2:108450343
|
G | T | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.63+654G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450343 | ||||||
chr2:108450610
|
G | A | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.64-418G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450610 | ||||||
chr2:108450647
|
C | T | 84 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.64-381C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450647 | ||||||
chr2:108450663
|
C | T | 1 | a0004c0007t0047g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-365C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450663 | ||||||
chr2:108450774
|
T | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-254T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450774 | ||||||
chr2:108450805
|
T | C | 247 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(244): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.64-223T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450805 | ||||||
chr2:108450881
|
C | T | 88 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0010others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.64-147C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450881 | ||||||
chr2:108450882
|
A | T | 1 | a0001c0002t0001g0009 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.64-146A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450882 | ||||||
chr2:108450903
|
G | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.64-125G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450903 | ||||||
chr2:108450904
|
T | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.64-124T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450904 | ||||||
chr2:108451169
|
G | A | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+57G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451169 | ||||||
chr2:108451232
|
T | G | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.148+120T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451232 | ||||||
chr2:108451320
|
T | G | 1 | a0002c0003t0003g0106 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.148+208T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451320 | ||||||
chr2:108451329
|
A | G | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.148+217A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451329 | ||||||
chr2:108451396
|
G | C | 1 | a0001c0001t0002g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.148+284G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451396 | ||||||
chr2:108451454
|
G | A | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+342G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451454 | ||||||
chr2:108451519
|
C | T | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.148+407C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451519 | ||||||
chr2:108451606
|
CT | C | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.148+504delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451606 | |||||
chr2:108451827
|
T | TTCTCTC | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-562_149-557dup others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451827 | |||||
chr2:108451841
|
C | CT | 17 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232others(14): Show | 18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-540dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451841 | |||||
chr2:108451841
|
C | CTT | 7 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(4): Show | 7 | HG01261.hp1 HG02647.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-541_149-540dup others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451841 | |||||
chr2:108451841
|
CT | C | 90 | a0001c0001t0016g0113a0001c0001t0044g0235a0001c0002t0001g0002others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.149-540delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451841 | |||||
chr2:108451859
|
T | C | 1 | a0001c0002t0008g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.149-540T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451859 | ||||||
chr2:108451936
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.149-463C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451936 | ||||||
chr2:108452032
|
C | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.149-367C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108452032 | ||||||
chr2:108452052
|
C | G | 6 | a0001c0001t0045g0153a0001c0006t0018g0146a0001c0006t0018g0148others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-347C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108452052 | ||||||
chr2:108452275
|
A | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.149-124A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108452275 | ||||||
chr2:108452552
|
T | C | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.216+86T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452552 | ||||||
chr2:108452691
|
C | CT | 17 | a0001c0001t0002g0176a0001c0001t0006g0228a0001c0001t0006g0229others(14): Show | 18 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.216+246dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | |||||
chr2:108452691
|
CT | C | 10 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(7): Show | 10 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+246delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | |||||
chr2:108452691
|
CTT | C | 7 | a0001c0001t0003g0105a0001c0001t0003g0145a0001c0002t0001g0083others(4): Show | 7 | HG00323.hp1 HG02559.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.216+245_216+246del others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | |||||
chr2:108452691
|
CTTT | C | 141 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(138): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.216+244_216+246del others(3): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | |||||
chr2:108452746
|
T | G | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+280T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452746 | ||||||
chr2:108452839
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.216+373G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452839 | ||||||
chr2:108452898
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.216+432T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452898 | ||||||
chr2:108452934
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.216+468C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452934 | ||||||
chr2:108452976
|
G | A | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.216+510G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452976 | ||||||
chr2:108452984
|
G | A | 1 | a0001c0001t0009g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.216+518G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452984 | ||||||
chr2:108453033
|
C | T | 1 | a0001c0001t0010g0251 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.216+567C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453033 | ||||||
chr2:108453073
|
T | C | 1 | a0001c0013t0046g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.216+607T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453073 | ||||||
chr2:108453100
|
A | G | 1 | a0003c0004t0031g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.216+634A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453100 | ||||||
chr2:108453109
|
T | C | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+643T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453109 | ||||||
chr2:108453482
|
C | T | 1 | a0001c0002t0001g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.216+1016C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453482 | ||||||
chr2:108453508
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.216+1042A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453508 | ||||||
chr2:108453645
|
C | T | 2 | a0001c0001t0004g0249a0001c0001t0042g0250 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.216+1179C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453645 | ||||||
chr2:108453785
|
T | TA | 9 | a0001c0001t0002g0152a0001c0001t0002g0185a0001c0001t0002g0254others(6): Show | 9 | HG01167.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.216+1336dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108453785 | |||||
chr2:108453785
|
TA | T | 137 | a0001c0001t0002g0226a0001c0001t0003g0114a0001c0001t0003g0116others(134): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.216+1336delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108453785 | |||||
chr2:108453785
|
TAA | T | 18 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(15): Show | 19 | HG00323.hp1 HG01074.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.216+1335_216+1336d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108453785 | |||||
chr2:108454009
|
G | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+1543G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454009 | ||||||
chr2:108454062
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+1596C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454062 | ||||||
chr2:108454100
|
C | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+1634C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454100 | ||||||
chr2:108454178
|
A | G | 168 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.216+1712A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454178 | ||||||
chr2:108454242
|
G | A | 14 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(11): Show | 15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+1776G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454242 | ||||||
chr2:108454437
|
G | T | 1 | a0001c0002t0001g0009 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.216+1971G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454437 | ||||||
chr2:108454670
|
C | G | 1 | a0001c0002t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.216+2204C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454670 | ||||||
chr2:108454714
|
C | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+2248C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454714 | ||||||
chr2:108454731
|
T | C | 2 | a0001c0002t0001g0012a0001c0002t0001g0013 | 2 | HG01928.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.216+2265T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454731 | ||||||
chr2:108454896
|
AT | A | 44 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(41): Show | 44 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.216+2441delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108454896 | |||||
chr2:108454963
|
G | A | 1 | a0001c0002t0001g0014 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.216+2497G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454963 | ||||||
chr2:108454977
|
CTA | C | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.216+2514_216+2515d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108454977 | |||||
chr2:108455017
|
A | G | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+2551A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455017 | ||||||
chr2:108455168
|
G | A | 1 | a0001c0001t0024g0257 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.216+2702G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455168 | ||||||
chr2:108455219
|
C | A | 13 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+2753C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455219 | ||||||
chr2:108455285
|
C | G | 1 | a0001c0001t0010g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.216+2819C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455285 | ||||||
chr2:108455366
|
G | A | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+2900G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455366 | ||||||
chr2:108455456
|
C | A | 1 | a0001c0001t0036g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.216+2990C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455456 | ||||||
chr2:108455475
|
ACCTTTAA others(3): Show |
A | 1 | a0001c0001t0002g0232 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.216+3010_216+3019d others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455475 | ||||||
chr2:108455518
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+3052C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455518 | ||||||
chr2:108455591
|
CAG | C | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+3128_216+3129d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108455591 | |||||
chr2:108455616
|
G | T | 6 | a0001c0001t0010g0256a0001c0001t0010g0264a0001c0001t0010g0265others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+3150G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455616 | ||||||
chr2:108455662
|
A | G | 1 | a0001c0002t0001g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.216+3196A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455662 | ||||||
chr2:108455720
|
G | A | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+3254G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455720 | ||||||
chr2:108455950
|
T | C | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.216+3484T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455950 | ||||||
chr2:108455958
|
C | G | 1 | a0002c0003t0003g0112 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.216+3492C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455958 | ||||||
chr2:108456007
|
C | T | 1 | a0001c0001t0010g0256 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.216+3541C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456007 | ||||||
chr2:108456025
|
C | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+3559C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456025 | ||||||
chr2:108456129
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.216+3663C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456129 | ||||||
chr2:108456237
|
G | A | 1 | a0001c0002t0001g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.216+3771G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456237 | ||||||
chr2:108456274
|
C | T | 1 | a0001c0008t0014g0160 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.216+3808C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456274 | ||||||
chr2:108456374
|
A | T | 1 | a0001c0001t0048g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.216+3908A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456374 | ||||||
chr2:108456673
|
A | G | 1 | a0001c0001t0004g0248 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.216+4207A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456673 | ||||||
chr2:108456720
|
G | A | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+4254G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456720 | ||||||
chr2:108456766
|
CAT | C | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+4302_216+4303d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456766 | |||||
chr2:108456948
|
T | TA | 40 | a0001c0001t0002g0186a0001c0001t0003g0004a0001c0001t0003g0096others(37): Show | 42 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.216+4501dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456948 | |||||
chr2:108456948
|
T | TAA | 21 | a0001c0001t0003g0114a0001c0001t0003g0116a0001c0001t0003g0117others(18): Show | 21 | HG01891.hp2 HG02602.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.216+4500_216+4501d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456948 | |||||
chr2:108456948
|
TA | T | 92 | a0001c0001t0002g0214a0001c0001t0006g0213a0001c0001t0045g0153others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.216+4501delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456948 | |||||
chr2:108456973
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.216+4507G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456973 | ||||||
chr2:108457061
|
A | G | 10 | a0001c0001t0045g0153a0001c0006t0018g0146a0001c0006t0018g0148others(7): Show | 10 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.216+4595A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457061 | ||||||
chr2:108457119
|
TATA | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+4657_216+4659d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108457119 | |||||
chr2:108457125
|
A | G | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+4659A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457125 | ||||||
chr2:108457248
|
G | A | 3 | a0001c0001t0002g0215a0001c0001t0027g0216a0001c0001t0029g0217 | 3 | HG02257.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.216+4782G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457248 | ||||||
chr2:108457390
|
G | T | 1 | a0004c0007t0047g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.216+4924G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457390 | ||||||
chr2:108457430
|
C | T | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+4964C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457430 | ||||||
chr2:108457545
|
G | C | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+5079G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457545 | ||||||
chr2:108457587
|
T | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+5121T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457587 | ||||||
chr2:108457587
|
T | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+5121T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457587 | ||||||
chr2:108457745
|
T | C | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+5279T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457745 | ||||||
chr2:108457908
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.216+5442C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457908 | ||||||
chr2:108458057
|
T | C | 7 | a0001c0002t0008g0017a0001c0002t0008g0018a0001c0002t0008g0019others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+5591T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458057 | ||||||
chr2:108458069
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.216+5603C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458069 | ||||||
chr2:108458181
|
C | T | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.216+5715C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458181 | ||||||
chr2:108458182
|
G | A | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+5716G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458182 | ||||||
chr2:108458238
|
A | T | 1 | a0001c0001t0002g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.216+5772A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458238 | ||||||
chr2:108458374
|
C | CT | 11 | a0001c0001t0003g0116a0001c0002t0001g0072a0001c0002t0001g0074others(8): Show | 11 | HG01192.hp1 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.216+5928dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | |||||
chr2:108458374
|
C | CTT | 53 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(50): Show | 54 | HG00323.hp1 HG01074.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.216+5927_216+5928d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | |||||
chr2:108458374
|
C | CTTT | 10 | a0001c0001t0003g0103a0001c0001t0003g0141a0001c0001t0003g0145others(7): Show | 11 | HG00639.hp1 HG01243.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+5926_216+5928d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | |||||
chr2:108458374
|
CT | C | 89 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0178others(86): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.216+5928delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | |||||
chr2:108458379
|
T | C | 3 | a0001c0001t0002g0187a0001c0002t0052g0156a0008c0016t0002g0188 | 3 | HG02965.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.216+5913T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458379 | ||||||
chr2:108458430
|
A | C | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+5964A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458430 | ||||||
chr2:108458446
|
G | A | 1 | a0001c0002t0001g0022 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.216+5980G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458446 | ||||||
chr2:108458521
|
T | C | 1 | a0001c0002t0001g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.216+6055T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458521 | ||||||
chr2:108458680
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.216+6214A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458680 | ||||||
chr2:108458904
|
C | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+6438C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458904 | ||||||
chr2:108459114
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.216+6648A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459114 | ||||||
chr2:108459245
|
G | T | 2 | a0003c0004t0030g0166a0003c0004t0031g0172 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.216+6779G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459245 | ||||||
chr2:108459252
|
G | A | 1 | a0001c0002t0001g0023 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.216+6786G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459252 | ||||||
chr2:108459276
|
G | A | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+6810G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459276 | ||||||
chr2:108459352
|
T | A | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+6886T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459352 | ||||||
chr2:108459481
|
C | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+7015C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459481 | ||||||
chr2:108459578
|
G | A | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.216+7112G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459578 | ||||||
chr2:108459649
|
A | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+7183A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459649 | ||||||
chr2:108459669
|
G | A | 11 | a0001c0001t0004g0001a0001c0001t0004g0237a0001c0001t0004g0238others(8): Show | 13 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+7203G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459669 | ||||||
chr2:108459745
|
C | CT | 28 | a0001c0001t0002g0007a0001c0001t0002g0176a0001c0001t0002g0178others(25): Show | 30 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.216+7312dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTT | 18 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0199others(15): Show | 18 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.216+7311_216+7312d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTT | 17 | a0001c0001t0002g0152a0001c0001t0002g0181a0001c0001t0002g0182others(14): Show | 17 | HG01109.hp2 HG01167.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.216+7310_216+7312d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTT | 9 | a0001c0001t0002g0207a0001c0001t0002g0214a0001c0001t0002g0224others(6): Show | 9 | HG00741.hp2 HG01993.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+7309_216+7312d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTT | 7 | a0001c0001t0002g0208a0001c0001t0028g0209a0001c0002t0001g0030others(4): Show | 7 | HG01167.hp1 HG01243.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+7308_216+7312d others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTT | 37 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(34): Show | 38 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.216+7307_216+7312d others(8): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT | 33 | a0001c0002t0001g0012a0001c0002t0001g0015a0001c0002t0001g0050others(30): Show | 33 | HG00323.hp2 HG01071.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+7306_216+7312d others(9): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(1): Show |
9 | a0001c0002t0001g0013a0001c0002t0001g0068a0001c0002t0001g0070others(6): Show | 9 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.216+7305_216+7312d others(10): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0013g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+7303_216+7312d others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(4): Show |
2 | a0001c0006t0018g0146a0001c0006t0032g0147 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.216+7302_216+7312d others(13): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0003g0119a0001c0001t0039g0137a0001c0002t0001g0071 | 3 | HG03654.hp2 NA18998.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.216+7301_216+7312d others(14): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(6): Show |
8 | a0001c0001t0003g0120a0001c0001t0003g0123a0001c0001t0005g0138others(5): Show | 8 | HG02486.hp2 HG02622.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+7300_216+7312d others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(9): Show |
1 | a0001c0006t0018g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.216+7297_216+7312d others(18): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(10): Show |
2 | a0002c0003t0003g0106a0002c0003t0003g0108 | 2 | NA19067.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.216+7296_216+7312d others(19): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0003g0125a0002c0003t0003g0109a0002c0003t0003g0111 | 3 | HG03491.hp1 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.216+7295_216+7312d others(20): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0017g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.216+7294_216+7312d others(21): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.216+7293_216+7312d others(22): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0116a0002c0003t0003g0110 | 2 | HG03239.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.216+7290_216+7312d others(25): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CT | C | 7 | a0001c0001t0002g0189a0001c0001t0002g0215a0001c0001t0027g0216others(4): Show | 7 | HG00642.hp2 HG01515.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+7312delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTT | C | 11 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(8): Show | 12 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.216+7310_216+7312d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTT | C | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0139others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+7309_216+7312d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTT | C | 6 | a0001c0001t0045g0153a0001c0002t0001g0023a0001c0002t0001g0024others(3): Show | 6 | HG02572.hp2 NA18747.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+7307_216+7312d others(8): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0003g0103a0001c0013t0046g0177a0003c0004t0031g0172 | 3 | HG02056.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.216+7300_216+7312d others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTTT others(7): Show |
C | 14 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(11): Show | 15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+7299_216+7312d others(16): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTTT others(9): Show |
C | 1 | a0005c0010t0020g0159 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.216+7297_216+7312d others(18): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTTT others(10): Show |
C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216+7296_216+7312d others(19): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+7294_216+7312d others(21): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459745
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+7293_216+7312d others(22): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | |||||
chr2:108459854
|
T | C | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+7388T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459854 | ||||||
chr2:108459889
|
C | T | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.216+7423C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459889 | ||||||
chr2:108459921
|
T | C | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.216+7455T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459921 | ||||||
chr2:108460001
|
T | C | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.216+7535T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460001 | ||||||
chr2:108460098
|
A | G | 246 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(243): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.216+7632A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460098 | ||||||
chr2:108460387
|
TC | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+7922delC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460387 | ||||||
chr2:108460400
|
C | T | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.216+7934C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460400 | ||||||
chr2:108460523
|
C | A | 1 | a0001c0001t0002g0187 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216+8057C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460523 | ||||||
chr2:108460524
|
C | T | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.216+8058C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460524 | ||||||
chr2:108460649
|
C | G | 1 | a0001c0001t0038g0247 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.216+8183C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460649 | ||||||
chr2:108460822
|
A | G | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.217-8158A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460822 | ||||||
chr2:108460860
|
C | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-8120C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460860 | ||||||
chr2:108460904
|
C | T | 1 | a0008c0016t0002g0188 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.217-8076C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460904 | ||||||
chr2:108460976
|
A | T | 8 | a0001c0001t0002g0007a0001c0001t0002g0176a0001c0001t0002g0225others(5): Show | 8 | HG01175.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-8004A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460976 | ||||||
chr2:108460994
|
C | A | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.217-7986C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460994 | ||||||
chr2:108461248
|
G | T | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-7732G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461248 | ||||||
chr2:108461291
|
AT | A | 72 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(69): Show | 74 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(71): Show |
intron_variant | MODIFIER | c.217-7678delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461291 | |||||
chr2:108461302
|
T | C | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-7678T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461302 | ||||||
chr2:108461348
|
G | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(6): Show | 9 | HG01167.hp2 HG01175.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-7632G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461348 | ||||||
chr2:108461460
|
A | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-7520A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461460 | ||||||
chr2:108461616
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.217-7364C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461616 | ||||||
chr2:108461658
|
A | G | 1 | a0001c0001t0003g0127 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.217-7322A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461658 | ||||||
chr2:108461693
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.217-7287G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461693 | ||||||
chr2:108461778
|
G | A | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-7202G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461778 | ||||||
chr2:108461830
|
C | CTTT | 54 | a0001c0001t0003g0004a0001c0001t0003g0099a0001c0001t0003g0102others(51): Show | 56 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.217-7147_217-7145d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461830 | |||||
chr2:108461830
|
C | CTTTTT | 5 | a0001c0001t0045g0153a0001c0006t0018g0148a0001c0006t0018g0149others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-7149_217-7145d others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461830 | |||||
chr2:108461836
|
C | CT | 11 | a0001c0001t0015g0244a0001c0002t0013g0088a0001c0002t0052g0156others(8): Show | 11 | HG00642.hp1 HG02040.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.217-7129dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461836 | |||||
chr2:108461836
|
C | T | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.217-7144C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461836 | ||||||
chr2:108461864
|
C | T | 3 | a0001c0001t0045g0153a0001c0019t0010g0154a0003c0004t0031g0172 | 3 | HG02572.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.217-7116C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461864 | ||||||
chr2:108461885
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.217-7095C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461885 | ||||||
chr2:108461999
|
A | AT | 90 | a0001c0001t0004g0255a0001c0001t0028g0209a0001c0002t0001g0002others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.217-6969dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461999 | |||||
chr2:108461999
|
A | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-6981A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461999 | ||||||
chr2:108462004
|
T | A | 1 | a0001c0001t0004g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.217-6976T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462004 | ||||||
chr2:108462073
|
G | A | 5 | a0001c0005t0001g0029a0001c0005t0001g0034a0001c0005t0001g0051others(2): Show | 5 | HG01167.hp1 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-6907G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462073 | ||||||
chr2:108462083
|
C | T | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.217-6897C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462083 | ||||||
chr2:108462084
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.217-6896G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462084 | ||||||
chr2:108462160
|
C | T | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.217-6820C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462160 | ||||||
chr2:108462241
|
C | G | 1 | a0001c0001t0002g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.217-6739C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462241 | ||||||
chr2:108462264
|
G | A | 13 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.217-6716G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462264 | ||||||
chr2:108462294
|
C | T | 1 | a0001c0001t0019g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.217-6686C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462294 | ||||||
chr2:108462336
|
A | T | 1 | a0001c0002t0001g0067 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.217-6644A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462336 | ||||||
chr2:108462411
|
G | A | 1 | a0001c0001t0053g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.217-6569G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462411 | ||||||
chr2:108462494
|
A | AAAAT | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-6468_217-6465d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462494 | |||||
chr2:108462524
|
C | G | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-6456C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462524 | ||||||
chr2:108462540
|
A | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-6440A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462540 | ||||||
chr2:108462541
|
TGTCACAA others(7): Show |
T | 86 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.217-6437_217-6424d others(16): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462541 | |||||
chr2:108462542
|
GTCACAAA others(2): Show |
G | 3 | a0001c0002t0001g0049a0001c0002t0001g0066a0001c0002t0008g0021 | 3 | HG00323.hp2 NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.217-6437_217-6429d others(11): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462542 | ||||||
chr2:108462555
|
CGCTT | C | 3 | a0001c0002t0001g0049a0001c0002t0001g0066a0001c0002t0008g0021 | 3 | HG00323.hp2 NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.217-6424_217-6421d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462555 | ||||||
chr2:108462560
|
C | CT | 9 | a0001c0001t0002g0189a0001c0001t0002g0232a0001c0001t0003g0120others(6): Show | 9 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-6400dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | |||||
chr2:108462560
|
C | CTT | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-6401_217-6400d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | |||||
chr2:108462560
|
C | CTTT | 5 | a0001c0001t0011g0129a0001c0001t0011g0151a0001c0001t0016g0124others(2): Show | 5 | HG02055.hp1 HG02886.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-6402_217-6400d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | |||||
chr2:108462560
|
C | T | 3 | a0001c0002t0001g0049a0001c0002t0001g0066a0001c0002t0008g0021 | 3 | HG00323.hp2 NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.217-6420C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462560 | ||||||
chr2:108462560
|
CT | C | 6 | a0001c0001t0006g0228a0001c0001t0010g0251a0001c0002t0008g0017others(3): Show | 6 | HG01167.hp1 HG01256.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-6400delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | |||||
chr2:108462597
|
C | T | 15 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(12): Show | 16 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.217-6383C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462597 | ||||||
chr2:108462624
|
G | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.217-6356G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462624 | ||||||
chr2:108462649
|
A | G | 1 | a0001c0001t0004g0237 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.217-6331A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462649 | ||||||
chr2:108462656
|
G | C | 3 | a0001c0002t0013g0088a0001c0002t0013g0089a0001c0002t0013g0090 | 3 | HG02559.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-6324G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462656 | ||||||
chr2:108462692
|
A | G | 1 | a0001c0019t0010g0154 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.217-6288A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462692 | ||||||
chr2:108462789
|
A | G | 1 | a0001c0002t0001g0079 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.217-6191A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462789 | ||||||
chr2:108462789
|
A | T | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.217-6191A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462789 | ||||||
chr2:108462838
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.217-6142C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462838 | ||||||
chr2:108462897
|
AT | A | 269 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(266): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.217-6072delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462897 | |||||
chr2:108462950
|
T | G | 1 | a0001c0001t0009g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.217-6030T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462950 | ||||||
chr2:108463438
|
A | G | 265 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.217-5542A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463438 | ||||||
chr2:108463446
|
G | A | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.217-5534G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463446 | ||||||
chr2:108463481
|
T | G | 1 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.217-5499T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463481 | ||||||
chr2:108463553
|
G | T | 3 | a0003c0004t0012g0168a0003c0004t0012g0171a0003c0004t0051g0169 | 3 | HG03195.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.217-5427G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463553 | ||||||
chr2:108463655
|
A | C | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.217-5325A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463655 | ||||||
chr2:108463745
|
G | T | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.217-5235G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463745 | ||||||
chr2:108463776
|
C | T | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-5204C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463776 | ||||||
chr2:108463959
|
T | G | 1 | a0001c0013t0046g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.217-5021T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463959 | ||||||
chr2:108463987
|
A | G | 1 | a0001c0001t0048g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.217-4993A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463987 | ||||||
chr2:108464010
|
G | A | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.217-4970G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464010 | ||||||
chr2:108464167
|
A | G | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-4813A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464167 | ||||||
chr2:108464282
|
G | C | 1 | a0001c0002t0001g0035 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.217-4698G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464282 | ||||||
chr2:108464286
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217-4694C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464286 | ||||||
chr2:108464367
|
G | C | 2 | a0001c0002t0013g0089a0001c0002t0013g0090 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-4613G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464367 | ||||||
chr2:108464458
|
G | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-4522G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464458 | ||||||
chr2:108464610
|
G | T | 65 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(62): Show | 67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-4370G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464610 | ||||||
chr2:108464643
|
G | T | 65 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(62): Show | 67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-4337G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464643 | ||||||
chr2:108464690
|
T | C | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.217-4290T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464690 | ||||||
chr2:108464740
|
A | C | 1 | a0001c0001t0002g0194 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.217-4240A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464740 | ||||||
chr2:108464745
|
A | T | 65 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(62): Show | 67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-4235A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464745 | ||||||
chr2:108464793
|
G | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.217-4187G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464793 | ||||||
chr2:108464899
|
T | G | 3 | a0004c0007t0022g0233a0004c0007t0022g0234a0004c0007t0047g0253 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.217-4081T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464899 | ||||||
chr2:108464930
|
C | T | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.217-4050C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464930 | ||||||
chr2:108465012
|
C | G | 40 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(37): Show | 41 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-3968C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465012 | ||||||
chr2:108465154
|
A | G | 1 | a0001c0002t0021g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.217-3826A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465154 | ||||||
chr2:108465232
|
T | G | 4 | a0001c0001t0003g0099a0001c0001t0003g0103a0001c0001t0017g0097others(1): Show | 4 | HG02056.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3748T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465232 | ||||||
chr2:108465293
|
C | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3687C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465293 | ||||||
chr2:108465356
|
CTT | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-3620_217-3619d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108465356 | |||||
chr2:108465461
|
A | G | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3519A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465461 | ||||||
chr2:108465596
|
A | T | 50 | a0001c0002t0001g0003a0001c0002t0001g0009a0001c0002t0001g0010others(47): Show | 51 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.217-3384A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465596 | ||||||
chr2:108465768
|
C | T | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.217-3212C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465768 | ||||||
chr2:108465919
|
A | C | 1 | a0001c0001t0009g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.217-3061A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465919 | ||||||
chr2:108465928
|
C | T | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3052C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465928 | ||||||
chr2:108466064
|
G | T | 1 | a0001c0001t0009g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.217-2916G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466064 | ||||||
chr2:108466185
|
C | G | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.217-2795C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466185 | ||||||
chr2:108466209
|
G | A | 65 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(62): Show | 67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-2771G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466209 | ||||||
chr2:108466249
|
G | A | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.217-2731G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466249 | ||||||
chr2:108466263
|
G | C | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.217-2717G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466263 | ||||||
chr2:108466343
|
C | T | 11 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(8): Show | 12 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-2637C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466343 | ||||||
chr2:108466464
|
T | TTTTA | 53 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(50): Show | 55 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.217-2496_217-2493d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108466464 | |||||
chr2:108466673
|
T | C | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.217-2307T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466673 | ||||||
chr2:108466757
|
C | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-2223C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466757 | ||||||
chr2:108466760
|
C | T | 1 | a0003c0004t0031g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.217-2220C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466760 | ||||||
chr2:108466935
|
T | A | 2 | a0001c0002t0013g0089a0001c0002t0013g0090 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-2045T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466935 | ||||||
chr2:108466943
|
T | A | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.217-2037T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466943 | ||||||
chr2:108466943
|
T | G | 1 | a0001c0002t0001g0058 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.217-2037T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466943 | ||||||
chr2:108467035
|
G | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-1945G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467035 | ||||||
chr2:108467361
|
A | G | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.217-1619A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467361 | ||||||
chr2:108467444
|
A | C | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-1536A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467444 | ||||||
chr2:108467651
|
G | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-1329G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467651 | ||||||
chr2:108467821
|
A | G | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-1159A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467821 | ||||||
chr2:108468067
|
CT | C | 165 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(162): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.217-901delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108468067 | |||||
chr2:108468145
|
C | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-835C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468145 | ||||||
chr2:108468369
|
A | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-611A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468369 | ||||||
chr2:108468375
|
A | G | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-605A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468375 | ||||||
chr2:108468486
|
A | AT | 7 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0139others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-485dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108468486 | |||||
chr2:108468651
|
A | C | 3 | a0001c0001t0002g0201a0001c0001t0002g0207a0001c0001t0002g0214 | 3 | HG00738.hp1 HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.217-329A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468651 | ||||||
chr2:108468756
|
C | T | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.217-224C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468756 | ||||||
chr2:108468852
|
A | AATGTGTT others(306): Show |
1 | a0001c0002t0001g0065 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.217-112_217-111ins others(313): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108468852 | |||||
chr2:108468852
|
A | G | 3 | a0001c0002t0001g0031a0001c0002t0001g0057a0001c0002t0001g0075 | 3 | HG03669.hp1 NA18955.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.217-128A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468852 | ||||||
chr2:108468917
|
A | G | 84 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.217-63A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468917 | ||||||
chr2:108469106
|
C | A | 1 | a0001c0002t0001g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.321+22C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 5/22 | chr2 | 108469106 | ||||||
chr2:108469198
|
CAAAG | C | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.321+118_321+121del others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 108469198 | |||||
chr2:108469532
|
A | G | 1 | a0001c0002t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.322-119A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 5/22 | chr2 | 108469532 | ||||||
chr2:108472137
|
A | G | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2787+21A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472137 | ||||||
chr2:108472179
|
G | A | 1 | a0001c0001t0004g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2787+63G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472179 | ||||||
chr2:108472222
|
A | AT | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+109dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 108472222 | |||||
chr2:108472256
|
A | G | 7 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0139others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2787+140A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472256 | ||||||
chr2:108472350
|
G | T | 65 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(62): Show | 67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.2787+234G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472350 | ||||||
chr2:108472412
|
G | A | 168 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.2787+296G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472412 | ||||||
chr2:108472540
|
A | G | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.2788-287A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472540 | ||||||
chr2:108472542
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-285T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472542 | ||||||
chr2:108472548
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-279T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472548 | ||||||
chr2:108472575
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-252T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472575 | ||||||
chr2:108472607
|
CT | C | 5 | a0001c0001t0045g0153a0001c0002t0023g0155a0001c0002t0023g0157others(2): Show | 5 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2788-207delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 108472607 | |||||
chr2:108472612
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-215T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472612 | ||||||
chr2:108472620
|
T | A | 1 | a0001c0001t0015g0245 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2788-207T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472620 | ||||||
chr2:108472644
|
T | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2788-183T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472644 | ||||||
chr2:108472803
|
T | G | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2788-24T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472803 | ||||||
chr2:108472948
|
C | G | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.2860+49C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108472948 | ||||||
chr2:108472954
|
G | A | 1 | a0004c0007t0047g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2860+55G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108472954 | ||||||
chr2:108473010
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2860+111C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473010 | ||||||
chr2:108473154
|
A | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+255A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473154 | ||||||
chr2:108473211
|
A | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2860+312A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473211 | ||||||
chr2:108473239
|
G | A | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860+340G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473239 | ||||||
chr2:108473289
|
A | G | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860+390A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473289 | ||||||
chr2:108473312
|
T | TA | 7 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0032g0147others(4): Show | 7 | HG01261.hp1 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+429dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 108473312 | |||||
chr2:108473312
|
TA | T | 132 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2860+429delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 108473312 | |||||
chr2:108473439
|
C | A | 2 | a0001c0002t0001g0041a0001c0002t0001g0074 | 2 | NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2860+540C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473439 | ||||||
chr2:108473483
|
C | A | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2860+584C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473483 | ||||||
chr2:108473496
|
A | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.2860+597A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473496 | ||||||
chr2:108473555
|
C | T | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2860+656C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473555 | ||||||
chr2:108473655
|
G | A | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.2860+756G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473655 | ||||||
chr2:108473730
|
G | T | 2 | a0001c0002t0008g0017a0001c0002t0008g0020 | 2 | HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2860+831G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473730 | ||||||
chr2:108473811
|
G | C | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860+912G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473811 | ||||||
chr2:108473882
|
G | A | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+983G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473882 | ||||||
chr2:108473891
|
C | T | 5 | a0001c0001t0003g0123a0001c0006t0018g0146a0001c0006t0018g0148others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+992C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473891 | ||||||
chr2:108473904
|
A | T | 44 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(41): Show | 44 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.2860+1005A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473904 | ||||||
chr2:108473928
|
C | T | 1 | a0001c0002t0001g0064 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2860+1029C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473928 | ||||||
chr2:108473954
|
C | T | 1 | a0001c0002t0035g0082 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2860+1055C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473954 | ||||||
chr2:108473982
|
T | C | 1 | a0001c0001t0003g0125 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2860+1083T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473982 | ||||||
chr2:108473996
|
C | CA | 90 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.2860+1109dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 108473996 | |||||
chr2:108474027
|
G | A | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2860+1128G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474027 | ||||||
chr2:108474051
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2860+1152G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474051 | ||||||
chr2:108474083
|
G | A | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.2860+1184G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474083 | ||||||
chr2:108474152
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2860+1253C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474152 | ||||||
chr2:108474190
|
A | G | 1 | a0003c0004t0012g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2860+1291A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474190 | ||||||
chr2:108474357
|
G | C | 2 | a0001c0002t0013g0089a0001c0002t0013g0090 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2861-1178G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474357 | ||||||
chr2:108474537
|
C | T | 1 | a0001c0001t0039g0137 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2861-998C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474537 | ||||||
chr2:108474538
|
A | G | 1 | a0001c0002t0001g0014 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2861-997A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474538 | ||||||
chr2:108474769
|
G | A | 1 | a0001c0001t0003g0131 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2861-766G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474769 | ||||||
chr2:108475023
|
C | G | 91 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.2861-512C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475023 | ||||||
chr2:108475099
|
G | C | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2861-436G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475099 | ||||||
chr2:108475313
|
A | C | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2861-222A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475313 | ||||||
chr2:108475353
|
A | G | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-182A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475353 | ||||||
chr2:108475360
|
G | A | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.2861-175G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475360 | ||||||
chr2:108475377
|
A | C | 14 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(11): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2861-158A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475377 | ||||||
chr2:108475458
|
C | T | 1 | a0001c0002t0001g0047 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2861-77C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475458 | ||||||
chr2:108475504
|
C | T | 1 | a0001c0001t0003g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2861-31C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475504 | ||||||
chr2:108475505
|
G | A | 1 | a0001c0001t0043g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2861-30G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475505 | ||||||
chr2:108475657
|
A | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2961+22A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 8/22 | chr2 | 108475657 | ||||||
chr2:108475665
|
G | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.2961+30G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 8/22 | chr2 | 108475665 | ||||||
chr2:108475689
|
A | G | 1 | a0003c0004t0030g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2961+54A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 8/22 | chr2 | 108475689 | ||||||
chr2:108475902
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3060+52C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108475902 | ||||||
chr2:108476023
|
C | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+173C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476023 | ||||||
chr2:108476054
|
C | CT | 34 | a0001c0001t0002g0182a0001c0001t0002g0189a0001c0001t0002g0190others(31): Show | 34 | HG00741.hp1 HG01106.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3060+230dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | |||||
chr2:108476054
|
C | CTTTTTTT others(4): Show |
2 | a0001c0008t0014g0160a0001c0008t0014g0161 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3060+220_3060+230d others(13): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | |||||
chr2:108476054
|
C | CTTTTTTT others(5): Show |
1 | a0001c0008t0014g0162 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3060+219_3060+230d others(14): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | |||||
chr2:108476054
|
C | CTTTTTTT others(6): Show |
1 | a0009c0017t0050g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3060+218_3060+230d others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | |||||
chr2:108476054
|
CT | C | 82 | a0001c0001t0002g0224a0001c0001t0006g0229a0001c0001t0045g0153others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.3060+230delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | |||||
chr2:108476054
|
CTTTTTTT others(3): Show |
C | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3060+221_3060+230d others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | |||||
chr2:108476055
|
T | C | 8 | a0001c0002t0001g0056a0001c0002t0001g0072a0001c0002t0001g0074others(5): Show | 8 | HG01361.hp2 HG01981.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.3060+205T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476055 | ||||||
chr2:108476056
|
T | C | 78 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.3060+206T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476056 | ||||||
chr2:108476090
|
T | G | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+240T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476090 | ||||||
chr2:108476125
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3060+275A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476125 | ||||||
chr2:108476206
|
C | T | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.3060+356C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476206 | ||||||
chr2:108476341
|
C | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+491C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476341 | ||||||
chr2:108476406
|
G | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.3060+556G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476406 | ||||||
chr2:108477047
|
T | C | 4 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0036others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3060+1197T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477047 | ||||||
chr2:108477063
|
A | C | 1 | a0001c0001t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3060+1213A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477063 | ||||||
chr2:108477214
|
C | T | 1 | a0001c0002t0035g0082 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3060+1364C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477214 | ||||||
chr2:108477360
|
C | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+1510C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477360 | ||||||
chr2:108477380
|
A | G | 70 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(67): Show | 72 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.3060+1530A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477380 | ||||||
chr2:108477392
|
C | T | 3 | a0001c0002t0001g0065a0001c0002t0001g0070a0010c0018t0001g0063 | 3 | HG00673.hp2 NA18997.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3060+1542C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477392 | ||||||
chr2:108477395
|
G | A | 1 | a0001c0002t0001g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3060+1545G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477395 | ||||||
chr2:108477405
|
T | C | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+1555T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477405 | ||||||
chr2:108477416
|
T | C | 7 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0139others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3060+1566T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477416 | ||||||
chr2:108477507
|
C | G | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3060+1657C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477507 | ||||||
chr2:108477764
|
G | A | 11 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(8): Show | 12 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.3060+1914G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477764 | ||||||
chr2:108477825
|
C | G | 1 | a0001c0001t0002g0208 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3060+1975C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477825 | ||||||
chr2:108477921
|
C | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3060+2071C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477921 | ||||||
chr2:108478070
|
G | GA | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+2221dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108478070 | |||||
chr2:108478127
|
A | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+2277A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478127 | ||||||
chr2:108478169
|
C | A | 2 | a0001c0002t0008g0017a0001c0002t0008g0020 | 2 | HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.3060+2319C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478169 | ||||||
chr2:108478201
|
G | A | 1 | a0001c0002t0001g0077 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3060+2351G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478201 | ||||||
chr2:108478237
|
T | TTGTATAA others(3): Show |
69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+2388_3060+238 others(14): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108478237 | |||||
chr2:108478240
|
G | GTATAATT others(6): Show |
69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+2391_3060+239 others(17): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108478240 | |||||
chr2:108478303
|
G | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(10): Show | 14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3060+2453G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478303 | ||||||
chr2:108478430
|
C | A | 1 | a0001c0001t0002g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3060+2580C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478430 | ||||||
chr2:108478491
|
T | C | 1 | a0002c0003t0003g0111 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3060+2641T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478491 | ||||||
chr2:108479100
|
G | C | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-2597G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479100 | ||||||
chr2:108479138
|
T | G | 2 | a0001c0001t0025g0095a0001c0001t0025g0100 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3061-2559T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479138 | ||||||
chr2:108479157
|
C | T | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3061-2540C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479157 | ||||||
chr2:108479180
|
A | G | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.3061-2517A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479180 | ||||||
chr2:108479261
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3061-2436G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479261 | ||||||
chr2:108479430
|
T | C | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.3061-2267T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479430 | ||||||
chr2:108479556
|
G | A | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3061-2141G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479556 | ||||||
chr2:108479635
|
T | C | 2 | a0004c0007t0022g0233a0004c0007t0022g0234 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3061-2062T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479635 | ||||||
chr2:108479663
|
G | A | 1 | a0002c0003t0003g0110 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3061-2034G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479663 | ||||||
chr2:108479816
|
T | C | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3061-1881T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479816 | ||||||
chr2:108479930
|
C | T | 14 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(11): Show | 15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.3061-1767C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479930 | ||||||
chr2:108479980
|
C | CA | 46 | a0001c0001t0002g0152a0001c0001t0002g0179a0001c0001t0002g0181others(43): Show | 46 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.3061-1688dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108479980
|
C | CAA | 15 | a0001c0001t0002g0007a0001c0001t0002g0176a0001c0001t0002g0223others(12): Show | 15 | HG01109.hp2 HG01175.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.3061-1689_3061-168 others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108479980
|
C | CAAA | 8 | a0001c0001t0002g0215a0001c0001t0007g0008a0001c0001t0007g0258others(5): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3061-1690_3061-168 others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108479980
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0011g0129a0001c0001t0011g0139a0001c0001t0016g0121others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3061-1698_3061-168 others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108479980
|
CAAAAAAA others(5): Show |
C | 62 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(59): Show | 64 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.3061-1699_3061-168 others(16): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108479980
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0002t0001g0042a0001c0002t0001g0048a0001c0002t0001g0049others(1): Show | 4 | HG02056.hp2 HG03927.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-1703_3061-168 others(20): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108479980
|
CAAAAAAA others(10): Show |
C | 83 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.3061-1704_3061-168 others(21): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | |||||
chr2:108480006
|
A | AC | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3061-1691_3061-169 others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480006 | ||||||
chr2:108480009
|
A | C | 69 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(66): Show | 71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3061-1688A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480009 | ||||||
chr2:108480211
|
C | A | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3061-1486C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480211 | ||||||
chr2:108480214
|
C | A | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3061-1483C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480214 | ||||||
chr2:108480448
|
C | A | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-1249C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480448 | ||||||
chr2:108480487
|
C | T | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.3061-1210C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480487 | ||||||
chr2:108480500
|
G | A | 1 | a0001c0001t0040g0173 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3061-1197G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480500 | ||||||
chr2:108480558
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0005g0136 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3061-1139A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480558 | ||||||
chr2:108480674
|
C | T | 1 | a0001c0001t0009g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3061-1023C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480674 | ||||||
chr2:108480678
|
C | T | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3061-1019C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480678 | ||||||
chr2:108480758
|
AG | A | 158 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(155): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.3061-935delG | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108480758 | |||||
chr2:108480845
|
C | T | 1 | a0001c0002t0008g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3061-852C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480845 | ||||||
chr2:108480870
|
TAAC | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.3061-824_3061-822d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108480870 | |||||
chr2:108480904
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3061-793G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480904 | ||||||
chr2:108480912
|
A | T | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3061-785A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480912 | ||||||
chr2:108481564
|
G | A | 7 | a0001c0002t0008g0017a0001c0002t0008g0018a0001c0002t0008g0019others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.3061-133G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108481564 | ||||||
chr2:108481928
|
C | A | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3180+112C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 10/22 | chr2 | 108481928 | ||||||
chr2:108482023
|
GTTGT | G | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3180+219_3180+222d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr2 | 108482023 | |||||
chr2:108482461
|
A | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3345+10A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482461 | ||||||
chr2:108482538
|
T | C | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.3345+87T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482538 | ||||||
chr2:108482542
|
A | G | 60 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(57): Show | 62 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.3345+91A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482542 | ||||||
chr2:108482700
|
G | A | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3345+249G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482700 | ||||||
chr2:108482780
|
C | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3346-282C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482780 | ||||||
chr2:108482870
|
C | T | 3 | a0004c0007t0022g0233a0004c0007t0022g0234a0004c0007t0047g0253 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3346-192C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482870 | ||||||
chr2:108482929
|
C | T | 52 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(49): Show | 54 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.3346-133C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482929 | ||||||
chr2:108482999
|
C | G | 1 | a0001c0001t0042g0250 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3346-63C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482999 | ||||||
chr2:108483021
|
A | G | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.3346-41A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108483021 | ||||||
chr2:108483250
|
A | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.3450+84A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483250 | ||||||
chr2:108483322
|
C | G | 2 | a0001c0001t0003g0119a0001c0001t0003g0123 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3450+156C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483322 | ||||||
chr2:108483369
|
A | G | 1 | a0001c0001t0005g0094 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3450+203A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483369 | ||||||
chr2:108483409
|
G | A | 101 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.3450+243G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483409 | ||||||
chr2:108483440
|
G | C | 1 | a0001c0002t0001g0091 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3450+274G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483440 | ||||||
chr2:108483484
|
C | A | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3450+318C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483484 | ||||||
chr2:108483621
|
A | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3450+455A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483621 | ||||||
chr2:108483882
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3451-267G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483882 | ||||||
chr2:108483926
|
A | T | 1 | a0001c0002t0008g0019 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3451-223A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483926 | ||||||
chr2:108484108
|
G | C | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3451-41G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108484108 | ||||||
chr2:108484354
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3613+43A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108484354 | ||||||
chr2:108485169
|
G | A | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3614-467G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485169 | ||||||
chr2:108485199
|
A | T | 1 | a0001c0001t0003g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3614-437A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485199 | ||||||
chr2:108485260
|
A | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3614-376A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485260 | ||||||
chr2:108485322
|
T | TA | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614-302dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 108485322 | |||||
chr2:108485574
|
T | C | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3614-62T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485574 | ||||||
chr2:108486035
|
C | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.3792+127C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486035 | ||||||
chr2:108486078
|
G | A | 185 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.3792+170G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486078 | ||||||
chr2:108486189
|
A | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3792+281A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486189 | ||||||
chr2:108486488
|
T | C | 1 | a0001c0001t0011g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3793-23T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486488 | ||||||
chr2:108486652
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
splice_region_variant&intron_variant | LOW | c.3930+4C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486652 | ||||||
chr2:108486808
|
A | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3930+160A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486808 | ||||||
chr2:108486822
|
C | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0075 | 2 | HG03669.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.3930+174C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486822 | ||||||
chr2:108486827
|
G | A | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3930+179G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486827 | ||||||
chr2:108487053
|
G | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.3930+405G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487053 | ||||||
chr2:108487166
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0005g0136 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3930+518A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487166 | ||||||
chr2:108487204
|
A | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3931-495A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487204 | ||||||
chr2:108487324
|
T | A | 14 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(11): Show | 15 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3931-375T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487324 | ||||||
chr2:108487381
|
A | G | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3931-318A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487381 | ||||||
chr2:108487900
|
A | AT | 11 | a0001c0001t0002g0201a0001c0001t0002g0205a0001c0001t0006g0229others(8): Show | 11 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.4052+103dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108487900 | |||||
chr2:108487900
|
AT | A | 56 | a0001c0001t0002g0215a0001c0001t0003g0004a0001c0001t0003g0096others(53): Show | 58 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.4052+103delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108487900 | |||||
chr2:108487900
|
ATT | A | 8 | a0001c0001t0003g0105a0001c0001t0011g0129a0001c0001t0011g0130others(5): Show | 8 | HG00323.hp1 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.4052+102_4052+103d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108487900 | |||||
chr2:108487901
|
T | A | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4052+81T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108487901 | ||||||
chr2:108487956
|
G | C | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4052+136G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108487956 | ||||||
chr2:108487992
|
G | A | 3 | a0001c0001t0002g0186a0001c0001t0002g0227a0001c0001t0019g0202 | 3 | HG02723.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4052+172G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108487992 | ||||||
chr2:108488008
|
G | C | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.4052+188G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488008 | ||||||
chr2:108488051
|
G | A | 1 | a0001c0001t0002g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4052+231G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488051 | ||||||
chr2:108488187
|
G | A | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4052+367G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488187 | ||||||
chr2:108488195
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4052+375C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488195 | ||||||
chr2:108488203
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4052+383G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488203 | ||||||
chr2:108488311
|
C | A | 1 | a0001c0001t0002g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4052+491C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488311 | ||||||
chr2:108488411
|
T | A | 1 | a0001c0001t0004g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4052+591T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488411 | ||||||
chr2:108488488
|
A | C | 1 | a0001c0001t0003g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4052+668A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488488 | ||||||
chr2:108488738
|
A | G | 245 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.4052+918A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488738 | ||||||
chr2:108488921
|
T | C | 1 | a0001c0002t0001g0030 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4053-917T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488921 | ||||||
chr2:108489146
|
A | C | 1 | a0001c0001t0010g0265 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4053-692A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489146 | ||||||
chr2:108489155
|
C | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4053-683C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489155 | ||||||
chr2:108489205
|
A | G | 32 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(29): Show | 32 | HG00099.hp2 HG00738.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.4053-633A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489205 | ||||||
chr2:108489376
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4053-462G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489376 | ||||||
chr2:108489395
|
G | A | 1 | a0001c0002t0001g0010 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4053-443G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489395 | ||||||
chr2:108489471
|
C | T | 8 | a0001c0002t0001g0033a0003c0004t0012g0167a0003c0004t0012g0168others(5): Show | 8 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.4053-367C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489471 | ||||||
chr2:108489514
|
C | CA | 6 | a0001c0001t0002g0199a0001c0001t0045g0153a0001c0002t0023g0155others(3): Show | 6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4053-311dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108489514 | |||||
chr2:108489678
|
T | TG | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4053-160_4053-159i others(3): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489678 | ||||||
chr2:108490037
|
C | T | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4229+23C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490037 | ||||||
chr2:108490222
|
A | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4229+208A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490222 | ||||||
chr2:108490585
|
T | TAA | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.4229+571_4229+572i others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490585 | ||||||
chr2:108490632
|
T | C | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4229+618T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490632 | ||||||
chr2:108490635
|
T | C | 1 | a0001c0001t0003g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4229+621T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490635 | ||||||
chr2:108490709
|
T | C | 1 | a0001c0001t0011g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4229+695T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490709 | ||||||
chr2:108490994
|
T | C | 1 | a0003c0004t0012g0171 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4229+980T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490994 | ||||||
chr2:108491067
|
T | C | 6 | a0001c0001t0010g0256a0001c0001t0010g0264a0001c0001t0010g0265others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4229+1053T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491067 | ||||||
chr2:108491093
|
T | TTATC | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4229+1083_4229+108 others(8): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 108491093 | |||||
chr2:108491198
|
A | T | 1 | a0004c0007t0047g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4229+1184A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491198 | ||||||
chr2:108491618
|
A | T | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4230-955A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491618 | ||||||
chr2:108491619
|
A | G | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4230-954A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491619 | ||||||
chr2:108491777
|
A | AT | 6 | a0001c0001t0003g0141a0001c0001t0003g0145a0001c0001t0005g0006others(3): Show | 7 | HG00639.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.4230-793dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 108491777 | |||||
chr2:108491780
|
T | A | 1 | a0001c0002t0023g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4230-793T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491780 | ||||||
chr2:108491781
|
A | T | 26 | a0001c0001t0003g0099a0001c0001t0003g0102a0001c0001t0003g0103others(23): Show | 28 | HG00323.hp1 HG00639.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4230-792A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491781 | ||||||
chr2:108491785
|
A | T | 126 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(123): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.4230-788A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491785 | ||||||
chr2:108491789
|
T | A | 1 | a0001c0001t0007g0263 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4230-784T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491789 | ||||||
chr2:108492004
|
T | C | 185 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.4230-569T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108492004 | ||||||
chr2:108492141
|
G | T | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4230-432G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108492141 | ||||||
chr2:108492142
|
T | G | 5 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.4230-431T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108492142 | ||||||
chr2:108492834
|
G | A | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4447+44G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492834 | ||||||
chr2:108492869
|
TAAGA | T | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4447+86_4447+89del others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 108492869 | |||||
chr2:108492887
|
A | G | 1 | a0010c0018t0001g0063 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4447+97A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492887 | ||||||
chr2:108492888
|
G | T | 1 | a0001c0015t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4447+98G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492888 | ||||||
chr2:108492963
|
C | A | 1 | a0002c0003t0003g0109 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.4447+173C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492963 | ||||||
chr2:108493016
|
C | T | 1 | a0001c0002t0021g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4447+226C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493016 | ||||||
chr2:108493085
|
G | A | 1 | a0001c0001t0003g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4447+295G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493085 | ||||||
chr2:108493153
|
G | A | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4447+363G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493153 | ||||||
chr2:108493158
|
C | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4447+368C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493158 | ||||||
chr2:108493241
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4447+451C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493241 | ||||||
chr2:108493264
|
A | G | 1 | a0001c0001t0010g0251 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4447+474A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493264 | ||||||
chr2:108493306
|
T | C | 1 | a0003c0004t0031g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4447+516T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493306 | ||||||
chr2:108493436
|
G | A | 1 | a0001c0001t0017g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4447+646G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493436 | ||||||
chr2:108493503
|
A | T | 1 | a0001c0001t0029g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4447+713A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493503 | ||||||
chr2:108493570
|
T | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4447+780T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493570 | ||||||
chr2:108493729
|
G | A | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4447+939G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493729 | ||||||
chr2:108493774
|
A | T | 1 | a0003c0004t0030g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4447+984A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493774 | ||||||
chr2:108493892
|
CA | C | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4447+1107delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 108493892 | |||||
chr2:108494123
|
C | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4448-1168C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494123 | ||||||
chr2:108494147
|
T | A | 1 | a0001c0001t0002g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4448-1144T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494147 | ||||||
chr2:108494202
|
A | G | 1 | a0001c0001t0005g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4448-1089A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494202 | ||||||
chr2:108494333
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4448-958C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494333 | ||||||
chr2:108494337
|
A | G | 3 | a0001c0001t0002g0215a0001c0001t0027g0216a0001c0001t0029g0217 | 3 | HG02257.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4448-954A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494337 | ||||||
chr2:108494560
|
A | C | 22 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118others(19): Show | 22 | HG02602.hp1 HG03017.hp2 HG03239.hp1 others(19): Show |
intron_variant | MODIFIER | c.4448-731A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494560 | ||||||
chr2:108494568
|
A | G | 1 | a0001c0002t0001g0012 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4448-723A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494568 | ||||||
chr2:108494572
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4448-719G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494572 | ||||||
chr2:108494605
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4448-686A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494605 | ||||||
chr2:108494731
|
A | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-560A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494731 | ||||||
chr2:108494766
|
T | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-525T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494766 | ||||||
chr2:108494779
|
G | C | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-512G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494779 | ||||||
chr2:108494783
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4448-508C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494783 | ||||||
chr2:108494787
|
T | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-504T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494787 | ||||||
chr2:108494801
|
T | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-490T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494801 | ||||||
chr2:108494803
|
C | G | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-488C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494803 | ||||||
chr2:108494807
|
G | C | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4448-484G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494807 | ||||||
chr2:108494813
|
G | T | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-478G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494813 | ||||||
chr2:108494819
|
T | TG | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-472_4448-471i others(3): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494819 | ||||||
chr2:108494821
|
G | T | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-470G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494821 | ||||||
chr2:108494826
|
G | T | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-465G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494826 | ||||||
chr2:108494839
|
A | C | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-452A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494839 | ||||||
chr2:108494845
|
A | G | 9 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(6): Show | 9 | HG02647.hp1 HG03486.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.4448-446A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494845 | ||||||
chr2:108494853
|
G | A | 2 | a0004c0007t0022g0233a0004c0007t0022g0234 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4448-438G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494853 | ||||||
chr2:108494868
|
A | G | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4448-423A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494868 | ||||||
chr2:108494890
|
G | A | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4448-401G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494890 | ||||||
chr2:108494908
|
T | C | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4448-383T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494908 | ||||||
chr2:108494929
|
A | G | 1 | a0001c0001t0045g0153 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4448-362A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494929 | ||||||
chr2:108494966
|
C | T | 10 | a0001c0001t0003g0104a0001c0001t0003g0127a0001c0006t0018g0146others(7): Show | 10 | HG01261.hp1 HG01981.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4448-325C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494966 | ||||||
chr2:108494971
|
C | G | 1 | a0001c0001t0004g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4448-320C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494971 | ||||||
chr2:108494977
|
G | A | 8 | a0001c0001t0004g0236a0001c0001t0011g0130a0001c0001t0011g0139others(5): Show | 8 | HG01243.hp2 HG02572.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.4448-314G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494977 | ||||||
chr2:108495031
|
T | C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4448-260T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495031 | ||||||
chr2:108495107
|
A | G | 7 | a0001c0001t0002g0196a0001c0001t0004g0255a0001c0001t0045g0153others(4): Show | 7 | HG02572.hp2 HG03453.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4448-184A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495107 | ||||||
chr2:108495110
|
T | C | 7 | a0001c0001t0002g0196a0001c0001t0004g0255a0001c0001t0045g0153others(4): Show | 7 | HG02572.hp2 HG03453.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4448-181T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495110 | ||||||
chr2:108495135
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4448-156C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495135 | ||||||
chr2:108495183
|
T | C | 3 | a0001c0001t0006g0175a0001c0001t0006g0184a0001c0001t0006g0228 | 3 | NA18942.hp1 NA18969.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.4448-108T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495183 | ||||||
chr2:108495204
|
T | G | 90 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.4448-87T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495204 | ||||||
chr2:108495224
|
T | C | 1 | a0001c0001t0015g0245 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4448-67T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495224 | ||||||
chr2:108495238
|
A | T | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4448-53A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495238 | ||||||
chr2:108495264
|
A | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4448-27A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495264 | ||||||
chr2:108495710
|
G | A | 2 | a0001c0002t0001g0058a0001c0002t0001g0060 | 2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.4642+225G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495710 | ||||||
chr2:108495741
|
G | A | 1 | a0001c0001t0002g0254 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4642+256G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495741 | ||||||
chr2:108495742
|
T | C | 1 | a0001c0001t0002g0254 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4642+257T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495742 | ||||||
chr2:108495802
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4642+317G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495802 | ||||||
chr2:108495810
|
CA | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4642+326delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495810 | ||||||
chr2:108495828
|
G | C | 2 | a0003c0004t0012g0167a0003c0004t0012g0170 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4642+343G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495828 | ||||||
chr2:108496031
|
A | G | 3 | a0001c0001t0002g0201a0001c0001t0002g0207a0001c0001t0002g0214 | 3 | HG00738.hp1 HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.4642+546A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496031 | ||||||
chr2:108496051
|
T | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4642+566T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496051 | ||||||
chr2:108496147
|
T | C | 1 | a0001c0001t0009g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4642+662T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496147 | ||||||
chr2:108496167
|
G | A | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4642+682G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496167 | ||||||
chr2:108496199
|
G | C | 185 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.4642+714G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496199 | ||||||
chr2:108496233
|
C | G | 2 | a0001c0002t0001g0054a0001c0002t0001g0068 | 2 | HG00099.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4643-737C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496233 | ||||||
chr2:108496244
|
A | T | 1 | a0010c0018t0001g0063 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4643-726A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496244 | ||||||
chr2:108496258
|
G | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4643-712G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496258 | ||||||
chr2:108496332
|
C | T | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4643-638C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496332 | ||||||
chr2:108496637
|
C | A | 1 | a0001c0001t0003g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4643-333C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496637 | ||||||
chr2:108496924
|
T | G | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4643-46T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496924 | ||||||
chr2:108496954
|
GAAC | G | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4643-11_4643-9delA others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 108496954 | |||||
chr2:108497234
|
A | G | 1 | a0004c0007t0047g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4782+125A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108497234 | ||||||
chr2:108497354
|
G | T | 5 | a0001c0002t0008g0018a0001c0002t0008g0019a0001c0002t0008g0021others(2): Show | 5 | HG00323.hp2 HG00639.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.4782+245G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108497354 | ||||||
chr2:108497622
|
T | C | 1 | a0001c0001t0009g0222 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4782+513T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108497622 | ||||||
chr2:108498101
|
T | C | 1 | a0001c0002t0001g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4782+992T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498101 | ||||||
chr2:108498102
|
G | C | 1 | a0001c0002t0001g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4782+993G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498102 | ||||||
chr2:108498121
|
G | A | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4782+1012G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498121 | ||||||
chr2:108498151
|
A | AACCTAAA others(1): Show |
4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4782+1043_4782+105 others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498151 | |||||
chr2:108498183
|
C | CT | 28 | a0001c0001t0002g0152a0001c0001t0002g0196a0001c0001t0002g0197others(25): Show | 28 | HG00673.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.4782+1104dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | |||||
chr2:108498183
|
C | CTT | 8 | a0001c0001t0002g0007a0001c0001t0002g0223a0001c0001t0002g0224others(5): Show | 8 | HG02280.hp1 HG02738.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4782+1103_4782+110 others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | |||||
chr2:108498183
|
C | CTTT | 9 | a0001c0001t0006g0229a0001c0001t0009g0219a0001c0001t0009g0220others(6): Show | 9 | HG01109.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4782+1102_4782+110 others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | |||||
chr2:108498183
|
CT | C | 95 | a0001c0001t0002g0199a0001c0001t0003g0116a0001c0001t0003g0117others(92): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.4782+1104delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | |||||
chr2:108498183
|
CTT | C | 9 | a0001c0001t0007g0008a0001c0001t0007g0258a0001c0001t0007g0259others(6): Show | 10 | HG01071.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.4782+1103_4782+110 others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | |||||
chr2:108498227
|
G | A | 1 | a0001c0001t0003g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4782+1118G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498227 | ||||||
chr2:108498235
|
T | A | 168 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.4782+1126T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498235 | ||||||
chr2:108498260
|
A | G | 2 | a0001c0002t0001g0011a0001c0002t0001g0022 | 2 | HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4782+1151A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498260 | ||||||
chr2:108498276
|
A | G | 1 | a0001c0001t0002g0196 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4782+1167A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498276 | ||||||
chr2:108498356
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4783-1197C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498356 | ||||||
chr2:108498485
|
C | T | 1 | a0001c0001t0006g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4783-1068C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498485 | ||||||
chr2:108498545
|
T | C | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4783-1008T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498545 | ||||||
chr2:108498651
|
C | T | 1 | a0001c0001t0011g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4783-902C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498651 | ||||||
chr2:108498736
|
A | G | 247 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(244): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4783-817A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498736 | ||||||
chr2:108498973
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4783-580C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498973 | ||||||
chr2:108499082
|
C | CTT | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.4783-471_4783-470i others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499082 | ||||||
chr2:108499194
|
C | G | 44 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(41): Show | 45 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.4783-359C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499194 | ||||||
chr2:108499210
|
A | G | 1 | a0003c0004t0051g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4783-343A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499210 | ||||||
chr2:108499278
|
C | T | 2 | a0004c0007t0022g0233a0004c0007t0022g0234 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4783-275C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499278 | ||||||
chr2:108499336
|
C | T | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4783-217C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499336 | ||||||
chr2:108499337
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4783-216G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499337 | ||||||
chr2:108499363
|
C | T | 1 | a0003c0004t0012g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4783-190C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499363 | ||||||
chr2:108499399
|
G | A | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4783-154G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499399 | ||||||
chr2:108499549
|
C | A | 1 | a0004c0007t0022g0234 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.4783-4C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499549 | ||||||
chr2:108499970
|
G | A | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4984+216G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108499970 | ||||||
chr2:108500157
|
CAT | C | 155 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.4984+409_4984+410d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108500157 | |||||
chr2:108500177
|
G | A | 7 | a0002c0003t0003g0106a0002c0003t0003g0107a0002c0003t0003g0108others(4): Show | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4984+423G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500177 | ||||||
chr2:108500243
|
G | A | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4984+489G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500243 | ||||||
chr2:108500329
|
A | G | 1 | a0001c0001t0002g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4984+575A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500329 | ||||||
chr2:108500390
|
A | G | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.4984+636A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500390 | ||||||
chr2:108500412
|
T | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4984+658T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500412 | ||||||
chr2:108500488
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4984+734G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500488 | ||||||
chr2:108500540
|
A | G | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4984+786A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500540 | ||||||
chr2:108500658
|
G | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4984+904G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500658 | ||||||
chr2:108500664
|
T | C | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4984+910T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500664 | ||||||
chr2:108500705
|
G | T | 91 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4984+951G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500705 | ||||||
chr2:108500768
|
T | G | 3 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162 | 3 | NA18954.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4984+1014T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500768 | ||||||
chr2:108500798
|
A | C | 7 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0001t0011g0139others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4984+1044A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500798 | ||||||
chr2:108500906
|
G | C | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4984+1152G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500906 | ||||||
chr2:108500997
|
C | T | 2 | a0001c0002t0001g0076a0009c0017t0050g0163 | 2 | HG01261.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.4984+1243C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500997 | ||||||
chr2:108501019
|
A | G | 5 | a0001c0002t0001g0028a0001c0002t0023g0155a0001c0002t0023g0157others(2): Show | 5 | HG01261.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4984+1265A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501019 | ||||||
chr2:108501059
|
G | A | 50 | a0001c0002t0001g0003a0001c0002t0001g0009a0001c0002t0001g0010others(47): Show | 51 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.4984+1305G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501059 | ||||||
chr2:108501082
|
G | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.4984+1328G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501082 | ||||||
chr2:108501087
|
C | T | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4984+1333C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501087 | ||||||
chr2:108501089
|
A | G | 1 | a0001c0002t0001g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4984+1335A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501089 | ||||||
chr2:108501098
|
C | T | 1 | a0001c0002t0001g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4984+1344C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501098 | ||||||
chr2:108501105
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4984+1351C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501105 | ||||||
chr2:108501113
|
A | G | 1 | a0001c0002t0001g0028 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4984+1359A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501113 | ||||||
chr2:108501121
|
C | A | 12 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(9): Show | 12 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.4984+1367C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501121 | ||||||
chr2:108501124
|
C | T | 12 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(9): Show | 12 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.4984+1370C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501124 | ||||||
chr2:108501130
|
G | A | 10 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(7): Show | 10 | HG01167.hp2 HG01175.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.4984+1376G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501130 | ||||||
chr2:108501145
|
G | A | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4984+1391G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501145 | ||||||
chr2:108501165
|
T | G | 1 | a0003c0004t0012g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4984+1411T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501165 | ||||||
chr2:108501175
|
C | T | 196 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(193): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.4984+1421C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501175 | ||||||
chr2:108501189
|
G | A | 201 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.4984+1435G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501189 | ||||||
chr2:108501217
|
C | T | 1 | a0001c0001t0017g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4984+1463C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501217 | ||||||
chr2:108501231
|
C | T | 1 | a0001c0001t0005g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4984+1477C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501231 | ||||||
chr2:108501232
|
G | A | 67 | a0001c0001t0002g0195a0001c0001t0007g0008a0001c0001t0007g0258others(64): Show | 69 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.4984+1478G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501232 | ||||||
chr2:108501270
|
C | A | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4984+1516C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501270 | ||||||
chr2:108501277
|
G | A | 150 | a0001c0001t0002g0186a0001c0001t0002g0191a0001c0001t0002g0227others(147): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.4984+1523G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501277 | ||||||
chr2:108501281
|
A | G | 4 | a0001c0001t0002g0205a0001c0002t0001g0014a0001c0002t0001g0040others(1): Show | 4 | HG02602.hp2 HG03834.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+1527A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501281 | ||||||
chr2:108501481
|
C | T | 5 | a0001c0001t0003g0132a0001c0008t0014g0160a0001c0008t0014g0161others(2): Show | 5 | HG01261.hp1 HG03710.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.4984+1727C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501481 | ||||||
chr2:108501519
|
A | G | 179 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(176): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.4984+1765A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501519 | ||||||
chr2:108501541
|
T | A | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4984+1787T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501541 | ||||||
chr2:108501582
|
T | C | 1 | a0001c0006t0018g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4984+1828T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501582 | ||||||
chr2:108501594
|
C | T | 4 | a0001c0001t0015g0242a0001c0001t0015g0244a0001c0001t0015g0245others(1): Show | 4 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4984+1840C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501594 | ||||||
chr2:108501676
|
G | C | 168 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.4984+1922G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501676 | ||||||
chr2:108501687
|
A | G | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+1933A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501687 | ||||||
chr2:108501771
|
A | T | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4984+2017A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501771 | ||||||
chr2:108501935
|
A | G | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4984+2181A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501935 | ||||||
chr2:108502204
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4984+2450A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502204 | ||||||
chr2:108502264
|
C | G | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.4984+2510C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502264 | ||||||
chr2:108502328
|
G | A | 63 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(60): Show | 65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.4984+2574G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502328 | ||||||
chr2:108502395
|
A | G | 52 | a0001c0002t0001g0003a0001c0002t0001g0009a0001c0002t0001g0010others(49): Show | 53 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.4984+2641A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502395 | ||||||
chr2:108502469
|
C | G | 2 | a0001c0002t0001g0044a0001c0002t0001g0048 | 2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.4984+2715C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502469 | ||||||
chr2:108502618
|
TACATTCT others(14): Show |
T | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4984+2865_4984+288 others(25): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502618 | ||||||
chr2:108502655
|
C | T | 158 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(155): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.4984+2901C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502655 | ||||||
chr2:108502656
|
A | G | 158 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(155): Show | 161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.4984+2902A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502656 | ||||||
chr2:108502721
|
T | C | 1 | a0010c0018t0001g0063 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4984+2967T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502721 | ||||||
chr2:108502749
|
C | T | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4984+2995C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502749 | ||||||
chr2:108502779
|
C | T | 1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4984+3025C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502779 | ||||||
chr2:108502811
|
T | A | 1 | a0001c0001t0002g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4984+3057T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502811 | ||||||
chr2:108502848
|
G | A | 5 | a0001c0001t0004g0238a0001c0001t0004g0240a0001c0001t0004g0246others(2): Show | 5 | HG00741.hp1 HG01106.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.4984+3094G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502848 | ||||||
chr2:108502897
|
C | T | 1 | a0001c0002t0001g0064 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4984+3143C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502897 | ||||||
chr2:108502898
|
G | A | 3 | a0001c0001t0002g0232a0001c0001t0002g0254a0001c0001t0011g0130 | 3 | HG03209.hp1 NA18997.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.4984+3144G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502898 | ||||||
chr2:108502911
|
A | G | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+3157A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502911 | ||||||
chr2:108502923
|
CA | C | 153 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(150): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.4984+3185delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108502923 | |||||
chr2:108502939
|
AG | A | 30 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(27): Show | 30 | HG00099.hp2 HG00738.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.4984+3186delG | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502939 | ||||||
chr2:108502940
|
G | A | 2 | a0001c0001t0006g0175a0001c0001t0006g0211 | 2 | NA18947.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.4984+3186G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502940 | ||||||
chr2:108502956
|
A | G | 4 | a0001c0008t0014g0160a0001c0008t0014g0161a0001c0008t0014g0162others(1): Show | 4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+3202A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502956 | ||||||
chr2:108503003
|
A | C | 4 | a0001c0006t0018g0146a0001c0006t0018g0148a0001c0006t0018g0149others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+3249A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503003 | ||||||
chr2:108503175
|
A | AG | 88 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.4984+3421_4984+342 others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503175 | ||||||
chr2:108503175
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4984+3421A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503175 | ||||||
chr2:108503178
|
G | A | 1 | a0001c0001t0029g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4984+3424G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503178 | ||||||
chr2:108503425
|
C | G | 4 | a0001c0001t0015g0242a0001c0001t0015g0244a0001c0001t0015g0245others(1): Show | 4 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4984+3671C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503425 | ||||||
chr2:108503627
|
G | A | 1 | a0001c0001t0028g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4984+3873G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503627 | ||||||
chr2:108503913
|
A | G | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0002t0052g0156 | 3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4985-3647A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503913 | ||||||
chr2:108503962
|
C | G | 161 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(158): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.4985-3598C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503962 | ||||||
chr2:108504020
|
A | T | 3 | a0001c0001t0002g0215a0001c0001t0027g0216a0001c0001t0029g0217 | 3 | HG02257.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4985-3540A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504020 | ||||||
chr2:108504099
|
A | G | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4985-3461A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504099 | ||||||
chr2:108504119
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4985-3441C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504119 | ||||||
chr2:108504123
|
A | T | 4 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0061others(1): Show | 4 | HG03669.hp1 HG03710.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.4985-3437A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504123 | ||||||
chr2:108504482
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4985-3078T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504482 | ||||||
chr2:108504585
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4985-2975C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504585 | ||||||
chr2:108504590
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4985-2970C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504590 | ||||||
chr2:108504759
|
T | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0200 | 2 | NA18940.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.4985-2801T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504759 | ||||||
chr2:108504789
|
T | G | 2 | a0005c0010t0020g0158a0005c0010t0020g0159 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4985-2771T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504789 | ||||||
chr2:108504951
|
C | A | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-2609C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504951 | ||||||
chr2:108504994
|
T | A | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-2566T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504994 | ||||||
chr2:108505027
|
C | T | 1 | a0001c0013t0046g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4985-2533C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505027 | ||||||
chr2:108505132
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4985-2428G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505132 | ||||||
chr2:108505138
|
C | G | 2 | a0004c0007t0022g0233a0004c0007t0022g0234 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4985-2422C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505138 | ||||||
chr2:108505160
|
A | C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4985-2400A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505160 | ||||||
chr2:108505187
|
T | G | 1 | a0001c0001t0038g0247 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4985-2373T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505187 | ||||||
chr2:108505261
|
C | T | 3 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0204 | 3 | HG01346.hp2 HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4985-2299C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505261 | ||||||
chr2:108505338
|
G | A | 1 | a0001c0001t0005g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4985-2222G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505338 | ||||||
chr2:108505451
|
G | C | 10 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(7): Show | 10 | HG01167.hp2 HG01175.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.4985-2109G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505451 | ||||||
chr2:108505629
|
G | A | 5 | a0001c0001t0019g0164a0001c0001t0045g0153a0001c0002t0013g0089others(2): Show | 5 | HG02572.hp2 HG02698.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4985-1931G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505629 | ||||||
chr2:108505643
|
A | G | 15 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(12): Show | 15 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.4985-1917A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505643 | ||||||
chr2:108505702
|
A | G | 2 | a0001c0001t0003g0119a0001c0001t0003g0123 | 2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4985-1858A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505702 | ||||||
chr2:108505708
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4985-1852C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505708 | ||||||
chr2:108505748
|
T | A | 168 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(165): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.4985-1812T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505748 | ||||||
chr2:108505770
|
G | C | 7 | a0003c0004t0012g0167a0003c0004t0012g0168a0003c0004t0012g0170others(4): Show | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4985-1790G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505770 | ||||||
chr2:108505879
|
G | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-1681G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505879 | ||||||
chr2:108505953
|
A | G | 1 | a0001c0001t0048g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4985-1607A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505953 | ||||||
chr2:108505958
|
A | T | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-1602A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505958 | ||||||
chr2:108506107
|
T | A | 1 | a0003c0004t0012g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4985-1453T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506107 | ||||||
chr2:108506330
|
C | G | 1 | a0001c0002t0001g0067 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4985-1230C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506330 | ||||||
chr2:108506406
|
G | GA | 23 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118others(20): Show | 23 | HG02602.hp1 HG02622.hp2 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.4985-1148dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108506406 | |||||
chr2:108506453
|
G | A | 1 | a0001c0013t0046g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4985-1107G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506453 | ||||||
chr2:108506578
|
C | T | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4985-982C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506578 | ||||||
chr2:108506654
|
T | C | 87 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4985-906T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506654 | ||||||
chr2:108506664
|
A | C | 2 | a0001c0001t0045g0153a0001c0019t0010g0154 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4985-896A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506664 | ||||||
chr2:108506737
|
T | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-823T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506737 | ||||||
chr2:108506775
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4985-785A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506775 | ||||||
chr2:108506814
|
G | A | 2 | a0001c0002t0023g0155a0001c0002t0023g0157 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4985-746G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506814 | ||||||
chr2:108506871
|
A | ATAGAGGA others(323): Show |
1 | a0001c0002t0052g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4985-685_4985-684i others(332): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108506871 | |||||
chr2:108506876
|
A | G | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-684A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506876 | ||||||
chr2:108507030
|
C | G | 2 | a0001c0002t0001g0041a0001c0002t0001g0074 | 2 | NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.4985-530C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507030 | ||||||
chr2:108507031
|
T | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4985-529T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507031 | ||||||
chr2:108507089
|
T | C | 4 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0180others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.4985-471T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507089 | ||||||
chr2:108507219
|
G | A | 1 | a0003c0004t0012g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4985-341G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507219 | ||||||
chr2:108507228
|
CA | C | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-324delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507228 | |||||
chr2:108507336
|
T | C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4985-224T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507336 | ||||||
chr2:108507404
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4985-156A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507404 | ||||||
chr2:108507405
|
A | AC | 92 | a0001c0001t0002g0192a0001c0001t0002g0214a0001c0001t0003g0103others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-144dupC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507405 | |||||
chr2:108507405
|
A | ACC | 28 | a0001c0001t0003g0118a0001c0001t0005g0138a0001c0002t0001g0012others(25): Show | 28 | HG01109.hp1 HG01192.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.4985-145_4985-144d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507405 | |||||
chr2:108507405
|
AC | A | 29 | a0001c0001t0002g0007a0001c0001t0002g0152a0001c0001t0002g0176others(26): Show | 29 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.4985-144delC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507405 | |||||
chr2:108507417
|
A | C | 3 | a0001c0002t0023g0155a0001c0002t0023g0157a0001c0012t0002g0203 | 3 | HG02895.hp1 HG02897.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.4985-143A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507417 | ||||||
chr2:108507494
|
T | A | 92 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0009others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4985-66T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507494 | ||||||
chr2:108507532
|
C | CT | 87 | a0001c0001t0027g0216a0001c0002t0001g0002a0001c0002t0001g0003others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4985-17dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507532 | |||||
chr2:108507532
|
C | CTT | 5 | a0001c0002t0008g0085a0001c0008t0014g0160a0001c0008t0014g0161others(2): Show | 5 | HG01261.hp1 HG03710.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.4985-18_4985-17dup others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507532 | |||||
chr2:108507540
|
T | G | 59 | a0001c0001t0003g0004a0001c0001t0003g0096a0001c0001t0003g0099others(56): Show | 61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4985-20T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507540 |