geneid | 22796 |
---|---|
ensemblid | ENSG00000135775.14 |
hgncid | 6546 |
symbol | COG2 |
name | component of oligomeric golgi complex 2 |
refseq_nuc | NM_007357.3 |
refseq_prot | NP_031383.1 |
ensembl_nuc | ENST00000366669.9 |
ensembl_prot | ENSP00000355629.4 |
mane_status | MANE Select |
chr | chr1 |
start | 230642481 |
end | 230693982 |
strand | + |
ver | v1.2 |
region | chr1:230642481-230693982 |
region5000 | chr1:230637481-230698982 |
regionname0 | COG2_chr1_230642481_230693982 |
regionname5000 | COG2_chr1_230637481_230698982 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 738 | 320 | 70 | 55 | 149 | 14 | 31 | 113 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002 | 0/0 | 738 | 43 | 3 | 9 | 21 | 4 | 6 | 17 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003 | 0/1 | 738 | 30 | 11 | 2 | 14 | 0 | 2 | 11 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0004 | 0/0 | 738 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0005 | 0/0 | 738 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0006 | 0/0 | 738 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0007 | 0/0 | 738 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0008 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0009 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0010 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0011 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2217 | 156 | 44 | 27 | 53 | 12 | 19 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0002 | 0/0 | 2217 | 147 | 15 | 27 | 93 | 1 | 11 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0003 | 0/0 | 2217 | 33 | 3 | 9 | 11 | 4 | 6 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0004 | 0/0 | 2217 | 26 | 10 | 1 | 14 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0005 | 0/0 | 2217 | 9 | 0 | 0 | 9 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0006 | 0/0 | 2217 | 6 | 5 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0007 | 0/0 | 2217 | 5 | 4 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0008 | 0/1 | 2217 | 3 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0009 | 0/0 | 2217 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0010 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0011 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0012 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0013 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0014 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0015 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0016 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0017 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0018 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0019 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0020 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0021 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0022 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0023 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0024 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0025 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0026 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
c0027 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 716 | 197 | 54 | 40 | 67 | 14 | 21 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0002 | 0/0 | 715 | 74 | 13 | 8 | 38 | 3 | 12 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0003 | 0/1 | 715 | 62 | 6 | 15 | 37 | 0 | 3 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0004 | 0/0 | 714 | 60 | 14 | 5 | 36 | 1 | 4 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0005 | 0/0 | 713 | 7 | 0 | 0 | 7 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0006 | 0/0 | 716 | 3 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0007 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
t0008 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 3 | 2 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0003 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0006 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0013 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0050 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2217 | 156 | 44 | 27 | 53 | 12 | 19 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0002 | 0/0 | 2217 | 147 | 15 | 27 | 93 | 1 | 11 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0006 | 0/0 | 2217 | 6 | 5 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0009 | 0/0 | 2217 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0010 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0012 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0013 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0014 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0018 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0019 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0020 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0021 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002c0003 | 0/0 | 2217 | 33 | 3 | 9 | 11 | 4 | 6 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002c0005 | 0/0 | 2217 | 9 | 0 | 0 | 9 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002c0023 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0004 | 0/0 | 2217 | 26 | 10 | 1 | 14 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0008 | 0/1 | 2217 | 3 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0015 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0004c0007 | 0/0 | 2217 | 5 | 4 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0005c0016 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0005c0017 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0006c0026 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0007c0022 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0008c0011 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0009c0024 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0010c0025 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0011c0027 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2932 | 89 | 27 | 22 | 23 | 9 | 7 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0001t0002 | 0/0 | 2931 | 62 | 13 | 5 | 29 | 3 | 12 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0001t0006 | 0/0 | 2932 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0001t0007 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0001t0008 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0002t0001 | 0/0 | 2932 | 27 | 0 | 8 | 14 | 0 | 5 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0002t0002 | 0/0 | 2931 | 8 | 0 | 1 | 7 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0002t0003 | 0/0 | 2931 | 53 | 1 | 13 | 36 | 0 | 3 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0002t0004 | 0/0 | 2930 | 59 | 14 | 5 | 36 | 1 | 3 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0006t0001 | 0/0 | 2932 | 6 | 5 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0009t0001 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0009t0002 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0010t0001 | 0/0 | 2932 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0012t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0013t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0014t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0018t0001 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0019t0002 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0020t0004 | 0/0 | 2930 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0001c0021t0006 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002c0003t0001 | 0/0 | 2932 | 33 | 3 | 9 | 11 | 4 | 6 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002c0005t0001 | 0/0 | 2932 | 9 | 0 | 0 | 9 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0002c0023t0003 | 0/0 | 2931 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0004t0001 | 0/0 | 2932 | 19 | 10 | 0 | 8 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0004t0002 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0004t0005 | 0/0 | 2929 | 6 | 0 | 0 | 6 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0008t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0008t0003 | 0/1 | 2931 | 2 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0003c0015t0001 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0004c0007t0003 | 0/0 | 2931 | 5 | 4 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0005c0016t0005 | 0/0 | 2929 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0005c0017t0001 | 0/0 | 2932 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0006c0026t0001 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0007c0022t0002 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0008c0011t0003 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0009c0024t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0010c0025t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
a0011c0027t0001 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | copy fasta | chr1 | 230637481 | 230698982 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0001 | 0/0 | 7 | 0 | 3 | 2 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0003 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0006 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0013 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0006t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0006t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0006t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0006t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0009t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0009t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0010t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0010t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0012t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0013t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0014t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0018t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0019t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0020t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0001c0021t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0005t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0005t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0005t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0002c0023t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0005g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0004t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0008t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0008t0003g0050 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0003c0015t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0007t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0007t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0007t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0007t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0004c0007t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0005c0016t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0005c0017t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0006c0026t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0007c0022t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0008c0011t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0009c0024t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0010c0025t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
a0011c0027t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0098 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0105 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00140 | hp1 | a0001 | c0018 | t0001 | g0065 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0215 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00408 | hp1 | a0003 | c0004 | t0001 | g0259 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00408 | hp2 | a0001 | c0002 | t0004 | g0167 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00438 | hp1 | a0001 | c0002 | t0004 | g0205 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00438 | hp2 | a0003 | c0004 | t0001 | g0273 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00544 | hp2 | a0003 | c0004 | t0001 | g0270 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0224 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00597 | hp2 | a0002 | c0005 | t0001 | g0010 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00609 | hp1 | a0001 | c0002 | t0004 | g0154 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0166 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00639 | hp1 | a0003 | c0008 | t0003 | g0050 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00639 | hp2 | a0001 | c0002 | t0004 | g0014 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | CHS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0301 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0086 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0033 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01074 | hp1 | a0001 | c0002 | t0004 | g0247 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01074 | hp2 | a0001 | c0002 | t0004 | g0013 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0035 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01106 | hp2 | a0007 | c0022 | t0002 | g0186 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01109 | hp1 | a0001 | c0006 | t0001 | g0047 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01109 | hp2 | a0003 | c0004 | t0002 | g0201 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0037 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01256 | hp1 | a0002 | c0003 | t0001 | g0112 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01257 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01261 | hp1 | a0004 | c0007 | t0003 | g0268 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01261 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01358 | hp1 | a0001 | c0002 | t0003 | g0029 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0037 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0104 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01515 | hp2 | a0002 | c0003 | t0001 | g0132 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0131 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01934 | hp1 | a0001 | c0002 | t0004 | g0040 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01934 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0082 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0081 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02027 | hp2 | a0002 | c0005 | t0001 | g0113 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02040 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02071 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02129 | hp2 | a0005 | c0017 | t0001 | g0087 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02135 | hp2 | a0001 | c0002 | t0004 | g0146 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0228 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | CDX | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0033 | AMR | PEL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02280 | hp1 | a0001 | c0013 | t0001 | g0048 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02280 | hp2 | a0001 | c0002 | t0004 | g0246 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0277 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02572 | hp2 | a0001 | c0012 | t0001 | g0090 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02615 | hp1 | a0003 | c0004 | t0001 | g0263 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02615 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02622 | hp1 | a0004 | c0007 | t0003 | g0264 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0108 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02717 | hp2 | a0002 | c0003 | t0001 | g0106 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02723 | hp2 | a0002 | c0003 | t0001 | g0114 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0097 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02818 | hp1 | a0001 | c0002 | t0004 | g0160 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0269 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02895 | hp1 | a0001 | c0021 | t0006 | g0116 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02896 | hp1 | a0003 | c0004 | t0001 | g0275 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0158 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02922 | hp1 | a0003 | c0004 | t0001 | g0267 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02965 | hp2 | a0003 | c0004 | t0001 | g0051 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02970 | hp1 | a0010 | c0025 | t0001 | g0092 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02970 | hp2 | a0003 | c0004 | t0001 | g0051 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03041 | hp1 | a0009 | c0024 | t0001 | g0091 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0177 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0048 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03139 | hp1 | a0001 | c0014 | t0001 | g0093 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0262 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03209 | hp2 | a0001 | c0006 | t0001 | g0244 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03225 | hp1 | a0011 | c0027 | t0001 | g0241 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03239 | hp1 | a0006 | c0026 | t0001 | g0297 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03453 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03486 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03490 | hp1 | a0002 | c0003 | t0001 | g0102 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0101 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0103 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03516 | hp2 | a0004 | c0007 | t0003 | g0251 | AFR | ESN | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0196 | AFR | GWD | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0305 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0144 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03669 | hp2 | a0001 | c0020 | t0004 | g0203 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03688 | hp1 | a0001 | c0002 | t0004 | g0176 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03704 | hp1 | a0003 | c0004 | t0001 | g0257 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0007 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03834 | hp2 | a0001 | c0002 | t0004 | g0242 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0095 | SAS | BEB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04199 | hp1 | a0003 | c0015 | t0001 | g0258 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0234 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0217 | SAS | STU | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18522 | hp2 | a0001 | c0006 | t0001 | g0245 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0107 | EAS | CHB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18747 | hp2 | a0001 | c0002 | t0004 | g0151 | EAS | CHB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0178 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18906 | hp2 | a0004 | c0007 | t0003 | g0265 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18942 | hp2 | a0003 | c0004 | t0001 | g0271 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0172 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18945 | hp2 | a0001 | c0002 | t0004 | g0206 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18948 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18949 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18950 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18951 | hp1 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18954 | hp1 | a0002 | c0023 | t0003 | g0111 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18954 | hp2 | a0001 | c0002 | t0004 | g0126 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18956 | hp1 | a0001 | c0009 | t0002 | g0208 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18956 | hp2 | a0001 | c0002 | t0004 | g0204 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18957 | hp2 | a0003 | c0004 | t0001 | g0276 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18959 | hp1 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18960 | hp1 | a0003 | c0004 | t0001 | g0261 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18964 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18967 | hp2 | a0003 | c0004 | t0005 | g0049 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18972 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18974 | hp1 | a0003 | c0004 | t0005 | g0254 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18979 | hp1 | a0002 | c0005 | t0001 | g0038 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18979 | hp2 | a0005 | c0016 | t0005 | g0252 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18981 | hp1 | a0002 | c0005 | t0001 | g0011 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18983 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18984 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18985 | hp2 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18988 | hp1 | a0001 | c0002 | t0004 | g0153 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18988 | hp2 | a0002 | c0005 | t0001 | g0010 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18989 | hp1 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18990 | hp1 | a0003 | c0004 | t0005 | g0255 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0169 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18991 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18991 | hp2 | a0001 | c0019 | t0002 | g0161 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0130 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18992 | hp2 | a0001 | c0002 | t0004 | g0162 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18994 | hp1 | a0003 | c0004 | t0005 | g0274 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18994 | hp2 | a0001 | c0002 | t0004 | g0128 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19000 | hp2 | a0003 | c0004 | t0005 | g0253 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19002 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19002 | hp2 | a0001 | c0009 | t0001 | g0046 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19003 | hp2 | a0002 | c0005 | t0001 | g0010 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19004 | hp2 | a0003 | c0004 | t0001 | g0272 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19006 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19007 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19010 | hp1 | a0003 | c0004 | t0005 | g0049 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19010 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19011 | hp1 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19030 | hp1 | a0003 | c0008 | t0001 | g0266 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19043 | hp2 | a0001 | c0010 | t0001 | g0279 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19054 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19056 | hp2 | a0001 | c0002 | t0004 | g0163 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19065 | hp1 | a0001 | c0002 | t0004 | g0159 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19065 | hp2 | a0002 | c0005 | t0001 | g0011 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19068 | hp1 | a0001 | c0001 | t0008 | g0221 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19070 | hp1 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19072 | hp1 | a0002 | c0003 | t0001 | g0096 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19072 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19076 | hp1 | a0003 | c0004 | t0001 | g0260 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19076 | hp2 | a0001 | c0002 | t0004 | g0148 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19077 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19078 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19079 | hp1 | a0002 | c0005 | t0001 | g0011 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19081 | hp2 | a0001 | c0002 | t0004 | g0152 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0195 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19085 | hp1 | a0001 | c0002 | t0004 | g0147 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19087 | hp1 | a0001 | c0002 | t0004 | g0123 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19088 | hp1 | a0001 | c0002 | t0004 | g0016 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19091 | hp1 | a0002 | c0005 | t0001 | g0038 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0170 | AFR | YRI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20129 | hp1 | a0001 | c0010 | t0001 | g0278 | AFR | ASW | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20129 | hp2 | a0001 | c0006 | t0001 | g0047 | AFR | ASW | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0013 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01123 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0129 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
HG06807 | hp2 | a0008 | c0011 | t0003 | g0089 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0243 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0003 | AFR | USA | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
NA21309 | hp2 | a0004 | c0007 | t0003 | g0256 | AFR | LWK | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
homoSapiens_chm13v2 | hp1 | a0003 | c0008 | t0003 | g0050 | REF | REF | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | COG2_chr1_230637481_230698982 | COG2 | chr1 | 230637481 | 230698982 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230659609
|
A | G | 1 | a0011 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.218A>G | p.Asn73Ser | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/18 | 344/2932 | 218/2217 | 73/738 | chr1 | 230659609 | ||
chr1:230663213
|
A | G | 1 | a0006 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.373A>G | p.Lys125Glu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/18 | 499/2932 | 373/2217 | 125/738 | chr1 | 230663213 | ||
chr1:230671550
|
A | G | 1 | a0010 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.809A>G | p.Asn270Ser | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/18 | 935/2932 | 809/2217 | 270/738 | chr1 | 230671550 | ||
chr1:230675010
|
T | A | 4 | a0003a0004a0005others(1): Show | 38 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(35): Show |
missense_variant | MODERATE | c.912T>A | p.Asn304Lys | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/18 | 1038/2932 | 912/2217 | 304/738 | chr1 | 230675010 | ||
chr1:230678922
|
A | G | 3 | a0002a0005a0009 | 46 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(43): Show |
missense_variant | MODERATE | c.1036A>G | p.Ile346Val | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/18 | 1162/2932 | 1036/2217 | 346/738 | chr1 | 230678922 | ||
chr1:230687082
|
C | T | 1 | a0009 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1528C>T | p.Arg510Cys | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/18 | 1654/2932 | 1528/2217 | 510/738 | chr1 | 230687082 | ||
chr1:230687086
|
C | G | 1 | a0007 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1532C>G | p.Thr511Ser | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/18 | 1658/2932 | 1532/2217 | 511/738 | chr1 | 230687086 | ||
chr1:230688533
|
G | A | 2 | a0004a0008 | 6 | HG01261.hp1 HG02622.hp1 HG03516.hp2 others(3): Show |
missense_variant | MODERATE | c.1765G>A | p.Val589Ile | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/18 | 1891/2932 | 1765/2217 | 589/738 | chr1 | 230688533 | ||
chr1:230693393
|
A | G | 5 | a0001a0002a0003others(2): Show | 160 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
stop_retained_variant | LOW | c.2217A>G | p.Ter739Ter | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 2343/2932 | 2217/2217 | 739/738 | chr1 | 230693393 | ||
chr1:230693981
|
CA | C | 5 | a0001a0002a0003others(2): Show | 122 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(119): Show |
splice_region_variant | LOW | c.*589delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | chr1 | 230693981 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230659574
|
C | T | 1 | a0001c0010 | 2 | NA19043.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.183C>T | p.Val61Val | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/18 | 309/2932 | 183/2217 | 61/738 | chr1 | 230659574 | ||
chr1:230660787
|
T | G | 4 | a0001c0006a0001c0012a0001c0013others(1): Show | 9 | HG01109.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.264T>G | p.Leu88Leu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/18 | 390/2932 | 264/2217 | 88/738 | chr1 | 230660787 | ||
chr1:230668757
|
C | T | 1 | a0001c0010 | 2 | NA19043.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.567C>T | p.Gly189Gly | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/18 | 693/2932 | 567/2217 | 189/738 | chr1 | 230668757 | ||
chr1:230671587
|
T | C | 1 | a0001c0014 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.846T>C | p.Phe282Phe | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/18 | 972/2932 | 846/2217 | 282/738 | chr1 | 230671587 | ||
chr1:230688469
|
G | A | 1 | a0001c0009 | 2 | NA18956.hp1 NA19002.hp2 |
synonymous_variant | LOW | c.1701G>A | p.Leu567Leu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/18 | 1827/2932 | 1701/2217 | 567/738 | chr1 | 230688469 | ||
chr1:230688508
|
C | T | 1 | a0001c0021 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1740C>T | p.Phe580Phe | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/18 | 1866/2932 | 1740/2217 | 580/738 | chr1 | 230688508 | ||
chr1:230690130
|
C | T | 1 | a0001c0013 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1911C>T | p.Gly637Gly | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/18 | 2037/2932 | 1911/2217 | 637/738 | chr1 | 230690130 | ||
chr1:230691426
|
G | A | 1 | a0001c0018 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.1977G>A | p.Lys659Lys | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/18 | 2103/2932 | 1977/2217 | 659/738 | chr1 | 230691426 | ||
chr1:230691483
|
C | T | 1 | a0001c0020 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.2034C>T | p.Pro678Pro | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/18 | 2160/2932 | 2034/2217 | 678/738 | chr1 | 230691483 | ||
chr1:230691486
|
C | T | 1 | a0003c0015 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.2037C>T | p.Val679Val | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/18 | 2163/2932 | 2037/2217 | 679/738 | chr1 | 230691486 | ||
chr1:230693342
|
C | T | 3 | a0001c0019a0002c0005a0005c0017 | 11 | HG00597.hp2 HG02027.hp2 HG02129.hp2 others(8): Show |
synonymous_variant | LOW | c.2166C>T | p.Leu722Leu | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 2292/2932 | 2166/2217 | 722/738 | chr1 | 230693342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230642497
|
AC | A | 9 | a0001c0001t0002a0001c0001t0007a0001c0002t0002others(6): Show | 136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
5_prime_UTR_variant | MODIFIER | c.-104delC | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/18 | 104 | INFO_REALIGN_3_PRIME | chr1 | 230642497 | ||||
chr1:230642499
|
C | T | 1 | a0001c0001t0008 | 1 | NA19068.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/18 | 108 | chr1 | 230642499 | |||||
chr1:230693530
|
C | T | 2 | a0001c0001t0006a0001c0021t0006 | 3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*137C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 137 | chr1 | 230693530 | |||||
chr1:230693551
|
C | T | 1 | a0001c0001t0007 | 2 | HG02976.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*158C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 158 | chr1 | 230693551 | |||||
chr1:230693951
|
ACCT | A | 2 | a0003c0004t0005a0005c0016t0005 | 7 | NA18967.hp2 NA18974.hp1 NA18979.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*562_*564delCCT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 18/18 | 562 | INFO_REALIGN_3_PRIME | chr1 | 230693951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:230642700
|
C | T | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72+22C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642700 | ||||||
chr1:230642745
|
G | C | 275 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(272): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.72+67G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642745 | ||||||
chr1:230642770
|
C | T | 1 | a0001c0002t0001g0281 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.72+92C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642770 | ||||||
chr1:230642785
|
G | T | 1 | a0001c0002t0004g0280 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.72+107G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642785 | ||||||
chr1:230642799
|
C | G | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+121C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230642799 | ||||||
chr1:230643085
|
C | T | 1 | a0001c0002t0003g0277 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.72+407C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643085 | ||||||
chr1:230643133
|
G | A | 42 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(39): Show | 56 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.72+455G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643133 | ||||||
chr1:230643327
|
T | G | 43 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(40): Show | 57 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.72+649T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643327 | ||||||
chr1:230643520
|
G | T | 73 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(70): Show | 90 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.72+842G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643520 | ||||||
chr1:230643589
|
G | GTTTTCTA others(1): Show |
269 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(266): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.72+918_72+919insTT others(6): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230643589 | |||||
chr1:230643664
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.72+986T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230643664 | ||||||
chr1:230644008
|
G | A | 45 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(42): Show | 59 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.72+1330G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644008 | ||||||
chr1:230644175
|
G | A | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72+1497G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644175 | ||||||
chr1:230644229
|
G | C | 71 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(68): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.72+1551G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644229 | ||||||
chr1:230644242
|
G | T | 1 | a0001c0001t0002g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72+1564G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644242 | ||||||
chr1:230644248
|
A | G | 73 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(70): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+1570A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644248 | ||||||
chr1:230644262
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.72+1584A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644262 | ||||||
chr1:230644489
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+1811G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644489 | ||||||
chr1:230644493
|
G | T | 1 | a0001c0002t0004g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+1815G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644493 | ||||||
chr1:230644589
|
C | T | 1 | a0001c0002t0004g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.72+1911C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644589 | ||||||
chr1:230644783
|
T | G | 1 | a0002c0003t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72+2105T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644783 | ||||||
chr1:230644802
|
A | G | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+2124A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644802 | ||||||
chr1:230644825
|
G | A | 268 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(265): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.72+2147G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644825 | ||||||
chr1:230644851
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72+2173G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644851 | ||||||
chr1:230644859
|
G | T | 1 | a0001c0002t0004g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.72+2181G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644859 | ||||||
chr1:230644978
|
T | G | 1 | a0001c0001t0002g0121 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.72+2300T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644978 | ||||||
chr1:230644997
|
A | G | 31 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(28): Show | 34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.72+2319A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230644997 | ||||||
chr1:230645233
|
CA | C | 127 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(124): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.72+2578delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230645233 | |||||
chr1:230645233
|
CAA | C | 167 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(164): Show | 218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.72+2577_72+2578del others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230645233 | |||||
chr1:230645252
|
A | G | 3 | a0002c0005t0001g0011a0002c0005t0001g0038a0002c0005t0001g0113 | 6 | HG02027.hp2 NA18979.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2574A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645252 | ||||||
chr1:230645253
|
A | G | 165 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(162): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.72+2575A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645253 | ||||||
chr1:230645482
|
C | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+2804C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645482 | ||||||
chr1:230645512
|
T | G | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72+2834T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645512 | ||||||
chr1:230645669
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(24): Show | 41 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+2991T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645669 | ||||||
chr1:230645700
|
C | T | 6 | a0003c0004t0001g0270a0003c0004t0001g0271a0003c0004t0001g0272others(3): Show | 6 | HG00438.hp2 HG00544.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3022C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645700 | ||||||
chr1:230645728
|
C | A | 1 | a0001c0002t0003g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.72+3050C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645728 | ||||||
chr1:230645728
|
C | G | 270 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(267): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.72+3050C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645728 | ||||||
chr1:230645763
|
G | A | 1 | a0005c0016t0005g0252 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.72+3085G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645763 | ||||||
chr1:230645792
|
A | G | 307 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(304): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.72+3114A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645792 | ||||||
chr1:230645861
|
C | T | 8 | a0003c0004t0001g0051a0003c0004t0001g0263a0003c0004t0001g0267others(5): Show | 9 | HG01261.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+3183C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645861 | ||||||
chr1:230645881
|
T | C | 275 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(272): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.72+3203T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645881 | ||||||
chr1:230645903
|
G | A | 1 | a0001c0002t0003g0130 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.72+3225G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645903 | ||||||
chr1:230645961
|
G | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0002c0003t0001g0131others(1): Show | 4 | HG00642.hp2 HG00741.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+3283G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645961 | ||||||
chr1:230645984
|
C | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0298others(3): Show | 9 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+3306C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645984 | ||||||
chr1:230645995
|
G | A | 117 | a0001c0001t0001g0061a0001c0001t0001g0127a0001c0001t0001g0171others(114): Show | 151 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.72+3317G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230645995 | ||||||
chr1:230646056
|
C | T | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+3378C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646056 | ||||||
chr1:230646069
|
T | G | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+3391T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646069 | ||||||
chr1:230646090
|
T | C | 1 | a0001c0002t0003g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.72+3412T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646090 | ||||||
chr1:230646248
|
C | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0216 | 3 | HG01192.hp2 HG01516.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.72+3570C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646248 | ||||||
chr1:230646309
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.72+3631G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646309 | ||||||
chr1:230646624
|
C | T | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72+3946C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646624 | ||||||
chr1:230646666
|
C | T | 112 | a0001c0001t0001g0127a0001c0001t0001g0171a0001c0001t0001g0213others(109): Show | 145 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.72+3988C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646666 | ||||||
chr1:230646701
|
GA | G | 70 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(67): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.72+4030delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230646701 | |||||
chr1:230646708
|
A | G | 1 | a0001c0002t0003g0085 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.72+4030A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646708 | ||||||
chr1:230646894
|
A | G | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.72+4216A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646894 | ||||||
chr1:230646988
|
G | A | 70 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(67): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.72+4310G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230646988 | ||||||
chr1:230647027
|
T | A | 1 | a0001c0002t0004g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+4349T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647027 | ||||||
chr1:230647070
|
G | A | 2 | a0002c0003t0001g0035a0009c0024t0001g0091 | 3 | HG01106.hp1 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.72+4392G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647070 | ||||||
chr1:230647245
|
C | T | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72+4567C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647245 | ||||||
chr1:230647331
|
C | T | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+4653C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647331 | ||||||
chr1:230647436
|
T | A | 1 | a0001c0001t0002g0136 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.72+4758T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647436 | ||||||
chr1:230647456
|
T | C | 37 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0046others(34): Show | 50 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.72+4778T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647456 | ||||||
chr1:230647522
|
A | C | 200 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0034others(197): Show | 255 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.72+4844A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647522 | ||||||
chr1:230647630
|
G | A | 30 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.72+4952G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647630 | ||||||
chr1:230647638
|
T | C | 8 | a0001c0001t0002g0012a0001c0001t0002g0137a0001c0001t0002g0138others(5): Show | 10 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+4960T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647638 | ||||||
chr1:230647700
|
C | T | 1 | a0004c0007t0003g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.72+5022C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647700 | ||||||
chr1:230647776
|
T | C | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5098T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647776 | ||||||
chr1:230647845
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.72+5167A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647845 | ||||||
chr1:230647857
|
ACT | A | 166 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(163): Show | 217 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.72+5182_72+5183del others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230647857 | |||||
chr1:230647903
|
C | T | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5225C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230647903 | ||||||
chr1:230648364
|
T | C | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5686T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648364 | ||||||
chr1:230648429
|
A | G | 1 | a0001c0002t0003g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.72+5751A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648429 | ||||||
chr1:230648460
|
A | G | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+5782A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648460 | ||||||
chr1:230648488
|
C | T | 2 | a0002c0005t0001g0011a0002c0005t0001g0038 | 5 | NA18979.hp1 NA18981.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+5810C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648488 | ||||||
chr1:230648529
|
C | A | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+5851C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648529 | ||||||
chr1:230648761
|
C | A | 17 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0120others(14): Show | 22 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+6083C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648761 | ||||||
chr1:230648820
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.72+6142C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648820 | ||||||
chr1:230648827
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72+6149C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648827 | ||||||
chr1:230648954
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+6276A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230648954 | ||||||
chr1:230649043
|
G | C | 28 | a0001c0001t0001g0100a0002c0003t0001g0004a0002c0003t0001g0036others(25): Show | 39 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.72+6365G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649043 | ||||||
chr1:230649059
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+6381C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649059 | ||||||
chr1:230649136
|
A | T | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+6458A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649136 | ||||||
chr1:230649156
|
C | T | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72+6478C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649156 | ||||||
chr1:230649198
|
C | T | 8 | a0001c0001t0002g0012a0001c0001t0002g0137a0001c0001t0002g0138others(5): Show | 10 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+6520C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649198 | ||||||
chr1:230649218
|
G | A | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+6540G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649218 | ||||||
chr1:230649535
|
T | G | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.72+6857T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649535 | ||||||
chr1:230649759
|
C | T | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+7081C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230649759 | ||||||
chr1:230650159
|
A | G | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+7481A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650159 | ||||||
chr1:230650425
|
A | G | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+7747A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650425 | ||||||
chr1:230650701
|
G | T | 2 | a0003c0004t0001g0262a0003c0004t0001g0275 | 2 | HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.72+8023G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650701 | ||||||
chr1:230650752
|
G | A | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+8074G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650752 | ||||||
chr1:230650869
|
T | G | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72+8191T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230650869 | ||||||
chr1:230651202
|
G | A | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-8262G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651202 | ||||||
chr1:230651221
|
T | C | 271 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(268): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.73-8243T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651221 | ||||||
chr1:230651222
|
G | A | 27 | a0001c0001t0001g0100a0002c0003t0001g0004a0002c0003t0001g0036others(24): Show | 38 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.73-8242G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651222 | ||||||
chr1:230651684
|
G | A | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-7780G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651684 | ||||||
chr1:230651701
|
C | A | 30 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-7763C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651701 | ||||||
chr1:230651849
|
T | C | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.73-7615T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230651849 | ||||||
chr1:230652190
|
G | A | 6 | a0003c0004t0005g0049a0003c0004t0005g0253a0003c0004t0005g0254others(3): Show | 7 | NA18967.hp2 NA18974.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-7274G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652190 | ||||||
chr1:230652207
|
C | CAGG | 275 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(272): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.73-7256_73-7255ins others(3): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230652207 | |||||
chr1:230652237
|
C | T | 1 | a0001c0002t0002g0212 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.73-7227C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652237 | ||||||
chr1:230652238
|
G | A | 1 | a0010c0025t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.73-7226G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652238 | ||||||
chr1:230652348
|
C | T | 1 | a0003c0004t0005g0255 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.73-7116C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652348 | ||||||
chr1:230652349
|
G | A | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-7115G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652349 | ||||||
chr1:230652431
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.73-7033C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652431 | ||||||
chr1:230652447
|
A | G | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-7017A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652447 | ||||||
chr1:230652470
|
A | G | 31 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(28): Show | 34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-6994A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652470 | ||||||
chr1:230652569
|
G | A | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(22): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.73-6895G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652569 | ||||||
chr1:230652755
|
T | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0094others(15): Show | 23 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-6709T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652755 | ||||||
chr1:230652804
|
C | T | 223 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0034others(220): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.73-6660C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230652804 | ||||||
chr1:230653013
|
G | A | 30 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-6451G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653013 | ||||||
chr1:230653073
|
C | T | 3 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG02258.hp1 HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.73-6391C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653073 | ||||||
chr1:230653148
|
G | A | 2 | a0002c0003t0001g0248a0002c0003t0001g0249 | 2 | NA18948.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.73-6316G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653148 | ||||||
chr1:230653221
|
G | GT | 65 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0094others(62): Show | 79 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.73-6229dupT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653221 | |||||
chr1:230653221
|
G | GTT | 10 | a0001c0001t0001g0232a0001c0001t0002g0211a0001c0002t0001g0229others(7): Show | 10 | HG00438.hp2 HG02083.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-6230_73-6229dup others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653221 | |||||
chr1:230653221
|
GT | G | 28 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(25): Show | 38 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.73-6229delT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653221 | |||||
chr1:230653234
|
T | G | 2 | a0001c0006t0001g0243a0001c0006t0001g0244 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.73-6230T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653234 | ||||||
chr1:230653235
|
T | G | 47 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(44): Show | 62 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.73-6229T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653235 | ||||||
chr1:230653325
|
A | G | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-6139A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653325 | ||||||
chr1:230653525
|
T | TTTGATTC others(30): Show |
1 | a0003c0004t0001g0275 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.73-5917_73-5881dup others(37): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653525 | |||||
chr1:230653525
|
T | TTTGATTC others(30): Show |
269 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(266): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.73-5915_73-5914ins others(37): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653525 | |||||
chr1:230653525
|
T | TTTGATTC others(30): Show |
1 | a0001c0002t0004g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-5915_73-5914ins others(37): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653525 | |||||
chr1:230653633
|
G | A | 222 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(219): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.73-5831G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653633 | ||||||
chr1:230653661
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.73-5803A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653661 | ||||||
chr1:230653701
|
T | C | 1 | a0001c0002t0003g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.73-5763T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653701 | ||||||
chr1:230653738
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73-5726C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653738 | ||||||
chr1:230653762
|
T | A | 1 | a0002c0003t0001g0096 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.73-5702T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653762 | ||||||
chr1:230653838
|
A | T | 1 | a0001c0002t0001g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.73-5626A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653838 | ||||||
chr1:230653855
|
T | C | 1 | a0001c0002t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.73-5609T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653855 | ||||||
chr1:230653923
|
C | CCTCATGA | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5539_73-5533dup others(7): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230653923 | |||||
chr1:230653946
|
A | C | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5518A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653946 | ||||||
chr1:230653983
|
G | C | 28 | a0001c0001t0001g0100a0002c0003t0001g0004a0002c0003t0001g0036others(25): Show | 39 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-5481G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230653983 | ||||||
chr1:230654038
|
T | C | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5426T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654038 | ||||||
chr1:230654461
|
A | G | 4 | a0001c0002t0003g0033a0001c0002t0003g0081a0001c0002t0003g0082others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-5003A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654461 | ||||||
chr1:230654667
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.73-4797A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654667 | ||||||
chr1:230654836
|
T | G | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-4628T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654836 | ||||||
chr1:230654888
|
C | G | 1 | a0001c0001t0001g0289 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.73-4576C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654888 | ||||||
chr1:230654922
|
C | G | 1 | a0001c0002t0003g0226 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.73-4542C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654922 | ||||||
chr1:230654947
|
G | A | 30 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.73-4517G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230654947 | ||||||
chr1:230655036
|
C | G | 1 | a0001c0001t0001g0026 | 3 | HG00741.hp2 HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.73-4428C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655036 | ||||||
chr1:230655317
|
A | G | 31 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(28): Show | 34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-4147A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655317 | ||||||
chr1:230655345
|
A | G | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.73-4119A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655345 | ||||||
chr1:230655412
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0282 | 5 | HG01069.hp1 HG01175.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-4052G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655412 | ||||||
chr1:230655414
|
G | C | 18 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0094others(15): Show | 23 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-4050G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655414 | ||||||
chr1:230655606
|
G | A | 1 | a0001c0020t0004g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73-3858G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655606 | ||||||
chr1:230655691
|
A | T | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.73-3773A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655691 | ||||||
chr1:230655882
|
G | A | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.73-3582G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655882 | ||||||
chr1:230655891
|
T | G | 40 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0063others(37): Show | 53 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.73-3573T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655891 | ||||||
chr1:230655900
|
T | C | 1 | a0001c0020t0004g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73-3564T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655900 | ||||||
chr1:230655917
|
C | G | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-3547C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230655917 | ||||||
chr1:230656092
|
G | A | 1 | a0008c0011t0003g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-3372G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656092 | ||||||
chr1:230656153
|
T | C | 1 | a0010c0025t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.73-3311T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656153 | ||||||
chr1:230656174
|
C | T | 1 | a0003c0004t0002g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.73-3290C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656174 | ||||||
chr1:230656178
|
A | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0094others(15): Show | 23 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-3286A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656178 | ||||||
chr1:230656286
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73-3178C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656286 | ||||||
chr1:230656312
|
G | A | 1 | a0001c0002t0003g0081 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.73-3152G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656312 | ||||||
chr1:230656431
|
G | T | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-3033G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656431 | ||||||
chr1:230656432
|
G | T | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-3032G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656432 | ||||||
chr1:230656438
|
G | A | 40 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(37): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.73-3026G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656438 | ||||||
chr1:230656496
|
A | G | 40 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(37): Show | 54 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.73-2968A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656496 | ||||||
chr1:230656631
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0006g0115a0001c0001t0006g0118others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-2833T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656631 | ||||||
chr1:230656778
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.73-2686A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230656778 | ||||||
chr1:230657065
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-2399T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657065 | ||||||
chr1:230657165
|
A | G | 1 | a0003c0004t0005g0254 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.73-2299A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657165 | ||||||
chr1:230657201
|
G | GGT | 224 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0034others(221): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.73-2263_73-2262ins others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657201 | ||||||
chr1:230657204
|
T | C | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-2260T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657204 | ||||||
chr1:230657261
|
G | A | 194 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0034others(191): Show | 248 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.73-2203G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657261 | ||||||
chr1:230657426
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-2038G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657426 | ||||||
chr1:230657641
|
G | C | 28 | a0001c0001t0001g0100a0002c0003t0001g0004a0002c0003t0001g0036others(25): Show | 39 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-1823G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657641 | ||||||
chr1:230657686
|
G | A | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1778G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657686 | ||||||
chr1:230657693
|
T | C | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1771T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657693 | ||||||
chr1:230657707
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0287a0001c0001t0001g0288 | 5 | HG00140.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-1757C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657707 | ||||||
chr1:230657768
|
T | C | 31 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(28): Show | 34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-1696T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657768 | ||||||
chr1:230657844
|
C | T | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1620C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657844 | ||||||
chr1:230657860
|
C | T | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1604C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657860 | ||||||
chr1:230657884
|
C | G | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1580C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657884 | ||||||
chr1:230657914
|
G | A | 22 | a0003c0004t0001g0257a0003c0004t0001g0259a0003c0004t0001g0260others(19): Show | 24 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.73-1550G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230657914 | ||||||
chr1:230658103
|
TC | T | 39 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0063others(36): Show | 52 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.73-1358delC | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr1 | 230658103 | |||||
chr1:230658208
|
T | C | 1 | a0001c0002t0001g0028 | 2 | NA18978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.73-1256T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658208 | ||||||
chr1:230658290
|
T | C | 1 | a0001c0001t0001g0023 | 3 | HG01243.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.73-1174T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658290 | ||||||
chr1:230658355
|
T | C | 1 | a0002c0003t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-1109T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658355 | ||||||
chr1:230658408
|
G | C | 30 | a0001c0001t0001g0100a0001c0010t0001g0278a0001c0010t0001g0279others(27): Show | 41 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-1056G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658408 | ||||||
chr1:230658433
|
C | T | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.73-1031C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658433 | ||||||
chr1:230658479
|
T | C | 2 | a0002c0003t0001g0036a0002c0003t0001g0098 | 3 | HG00099.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.73-985T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658479 | ||||||
chr1:230658480
|
G | A | 223 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(220): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.73-984G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658480 | ||||||
chr1:230658504
|
G | T | 1 | a0002c0003t0001g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.73-960G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658504 | ||||||
chr1:230658517
|
G | T | 1 | a0004c0007t0003g0268 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.73-947G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658517 | ||||||
chr1:230658683
|
C | T | 2 | a0001c0002t0003g0224a0001c0002t0003g0225 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.73-781C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658683 | ||||||
chr1:230658835
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.73-629A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230658835 | ||||||
chr1:230659038
|
A | G | 2 | a0003c0004t0001g0260a0003c0004t0001g0261 | 2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.73-426A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659038 | ||||||
chr1:230659090
|
A | T | 1 | a0008c0011t0003g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-374A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659090 | ||||||
chr1:230659156
|
T | A | 3 | a0002c0003t0001g0096a0002c0003t0001g0099a0002c0003t0001g0109 | 3 | NA18961.hp1 NA18964.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.73-308T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659156 | ||||||
chr1:230659431
|
T | C | 243 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(240): Show | 311 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.73-33T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 1/17 | chr1 | 230659431 | ||||||
chr1:230659795
|
A | G | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+170A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230659795 | ||||||
chr1:230659895
|
A | G | 196 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0034others(193): Show | 250 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.234+270A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230659895 | ||||||
chr1:230660212
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235-546G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660212 | ||||||
chr1:230660227
|
G | A | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-531G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660227 | ||||||
chr1:230660267
|
A | G | 2 | a0001c0001t0002g0198a0001c0001t0007g0042 | 3 | HG02976.hp2 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.235-491A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660267 | ||||||
chr1:230660382
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-376T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660382 | ||||||
chr1:230660468
|
A | G | 1 | a0001c0002t0003g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.235-290A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660468 | ||||||
chr1:230660494
|
C | T | 30 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.235-264C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660494 | ||||||
chr1:230660580
|
A | G | 41 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(38): Show | 55 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.235-178A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660580 | ||||||
chr1:230660629
|
A | C | 113 | a0001c0001t0001g0127a0001c0001t0001g0171a0001c0001t0001g0213others(110): Show | 146 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.235-129A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660629 | ||||||
chr1:230660633
|
A | G | 1 | a0003c0004t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235-125A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 2/17 | chr1 | 230660633 | ||||||
chr1:230660995
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.300+172G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230660995 | ||||||
chr1:230661126
|
CAT | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0282 | 5 | HG01069.hp1 HG01175.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.300+306_300+307del others(2): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr1 | 230661126 | |||||
chr1:230661320
|
G | A | 273 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(270): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.300+497G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661320 | ||||||
chr1:230661354
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.300+531A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661354 | ||||||
chr1:230661386
|
C | T | 2 | a0003c0004t0002g0201a0004c0007t0003g0268 | 2 | HG01109.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.300+563C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661386 | ||||||
chr1:230661490
|
C | T | 1 | a0001c0002t0003g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.300+667C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661490 | ||||||
chr1:230661579
|
C | A | 24 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(21): Show | 35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.300+756C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661579 | ||||||
chr1:230661758
|
A | G | 2 | a0001c0001t0002g0197a0001c0001t0002g0210 | 2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.300+935A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661758 | ||||||
chr1:230661794
|
A | G | 1 | a0001c0002t0004g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.300+971A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661794 | ||||||
chr1:230661872
|
A | T | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.300+1049A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661872 | ||||||
chr1:230661944
|
T | C | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.300+1121T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230661944 | ||||||
chr1:230662064
|
A | G | 1 | a0001c0002t0003g0125 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.301-1077A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662064 | ||||||
chr1:230662209
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0302 | 3 | HG02818.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.301-932C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662209 | ||||||
chr1:230662245
|
C | A | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.301-896C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662245 | ||||||
chr1:230662350
|
A | G | 1 | a0001c0002t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.301-791A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662350 | ||||||
chr1:230662509
|
C | A | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.301-632C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230662509 | ||||||
chr1:230663017
|
A | G | 1 | a0009c0024t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-124A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230663017 | ||||||
chr1:230663060
|
C | T | 1 | a0001c0001t0007g0042 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.301-81C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230663060 | ||||||
chr1:230663062
|
G | A | 24 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(21): Show | 35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.301-79G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 3/17 | chr1 | 230663062 | ||||||
chr1:230663537
|
T | G | 1 | a0002c0003t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.381+316T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230663537 | ||||||
chr1:230663752
|
G | A | 7 | a0003c0004t0005g0049a0003c0004t0005g0253a0003c0004t0005g0254others(4): Show | 8 | NA18967.hp2 NA18974.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+531G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230663752 | ||||||
chr1:230663797
|
A | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02080.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.381+576A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230663797 | ||||||
chr1:230664087
|
G | A | 1 | a0003c0004t0001g0129 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382-397G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664087 | ||||||
chr1:230664238
|
C | CA | 8 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-235dupA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr1 | 230664238 | |||||
chr1:230664371
|
T | C | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-113T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664371 | ||||||
chr1:230664384
|
G | A | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-100G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664384 | ||||||
chr1:230664448
|
A | G | 2 | a0001c0002t0003g0224a0001c0002t0003g0225 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.382-36A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 4/17 | chr1 | 230664448 | ||||||
chr1:230664710
|
T | C | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+123T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230664710 | ||||||
chr1:230665013
|
T | C | 1 | a0001c0001t0001g0023 | 3 | HG01243.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.485+426T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665013 | ||||||
chr1:230665119
|
C | T | 1 | a0003c0004t0005g0254 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.485+532C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665119 | ||||||
chr1:230665130
|
T | C | 1 | a0003c0004t0001g0270 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.485+543T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665130 | ||||||
chr1:230665201
|
A | G | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(22): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.485+614A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665201 | ||||||
chr1:230665247
|
G | A | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+660G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665247 | ||||||
chr1:230665283
|
C | T | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+696C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665283 | ||||||
chr1:230665301
|
A | G | 1 | a0003c0004t0002g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.485+714A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665301 | ||||||
chr1:230665444
|
A | C | 1 | a0001c0002t0003g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.485+857A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665444 | ||||||
chr1:230665475
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+888G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665475 | ||||||
chr1:230665494
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.485+907G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665494 | ||||||
chr1:230665784
|
A | G | 307 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(304): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.485+1197A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665784 | ||||||
chr1:230665795
|
C | T | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+1208C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665795 | ||||||
chr1:230665797
|
A | T | 2 | a0001c0002t0004g0128a0001c0002t0004g0195 | 2 | NA18994.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.485+1210A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665797 | ||||||
chr1:230665988
|
G | A | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+1401G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230665988 | ||||||
chr1:230666269
|
C | T | 32 | a0001c0001t0002g0005a0001c0001t0002g0017a0001c0001t0002g0018others(29): Show | 43 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+1682C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666269 | ||||||
chr1:230666613
|
T | G | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.485+2026T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666613 | ||||||
chr1:230666691
|
A | G | 1 | a0001c0002t0002g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486-1985A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666691 | ||||||
chr1:230666796
|
A | G | 1 | a0003c0004t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-1880A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230666796 | ||||||
chr1:230667116
|
G | C | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-1560G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667116 | ||||||
chr1:230667125
|
G | C | 1 | a0001c0002t0004g0204 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.486-1551G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667125 | ||||||
chr1:230667134
|
G | T | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.486-1542G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667134 | ||||||
chr1:230667179
|
G | A | 4 | a0001c0002t0004g0128a0001c0002t0004g0146a0001c0002t0004g0147others(1): Show | 4 | HG02135.hp2 NA18994.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-1497G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667179 | ||||||
chr1:230667206
|
C | T | 1 | a0002c0003t0001g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.486-1470C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667206 | ||||||
chr1:230667226
|
C | T | 24 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(21): Show | 35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.486-1450C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667226 | ||||||
chr1:230667328
|
G | C | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.486-1348G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667328 | ||||||
chr1:230667478
|
G | A | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.486-1198G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667478 | ||||||
chr1:230667534
|
A | G | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-1142A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667534 | ||||||
chr1:230667716
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486-960G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230667716 | ||||||
chr1:230667786
|
AGGGACAT others(15): Show |
A | 2 | a0001c0001t0001g0079a0001c0002t0001g0078 | 2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.486-887_486-866del others(22): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 230667786 | |||||
chr1:230668072
|
A | G | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.486-604A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668072 | ||||||
chr1:230668288
|
T | A | 10 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(7): Show | 11 | HG01109.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-388T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668288 | ||||||
chr1:230668297
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.486-379G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668297 | ||||||
chr1:230668334
|
T | A | 1 | a0001c0002t0004g0148 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.486-342T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668334 | ||||||
chr1:230668409
|
G | A | 1 | a0001c0002t0004g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.486-267G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668409 | ||||||
chr1:230668426
|
T | G | 1 | a0001c0001t0002g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.486-250T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668426 | ||||||
chr1:230668453
|
C | T | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.486-223C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668453 | ||||||
chr1:230668453
|
CG | C | 30 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.486-221delG | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr1 | 230668453 | |||||
chr1:230668607
|
G | T | 1 | a0001c0001t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486-69G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 5/17 | chr1 | 230668607 | ||||||
chr1:230668855
|
A | G | 1 | a0001c0002t0003g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.594+71A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230668855 | ||||||
chr1:230668873
|
G | A | 1 | a0003c0004t0002g0201 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.594+89G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230668873 | ||||||
chr1:230669027
|
C | T | 57 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0039others(54): Show | 76 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.594+243C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669027 | ||||||
chr1:230669076
|
A | C | 6 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 8 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-280A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669076 | ||||||
chr1:230669112
|
T | C | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.595-244T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669112 | ||||||
chr1:230669318
|
C | G | 1 | a0001c0002t0003g0077 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.595-38C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 6/17 | chr1 | 230669318 | ||||||
chr1:230669736
|
C | T | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+201C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230669736 | ||||||
chr1:230669768
|
G | A | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+233G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230669768 | ||||||
chr1:230669917
|
G | A | 1 | a0003c0004t0005g0255 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.774+382G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230669917 | ||||||
chr1:230670040
|
G | A | 31 | a0003c0004t0001g0051a0003c0004t0001g0257a0003c0004t0001g0259others(28): Show | 34 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.774+505G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670040 | ||||||
chr1:230670212
|
A | G | 2 | a0001c0002t0003g0007a0001c0002t0003g0230 | 5 | HG02083.hp1 HG02165.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+677A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670212 | ||||||
chr1:230670314
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.774+779C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670314 | ||||||
chr1:230670332
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.774+797C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670332 | ||||||
chr1:230670568
|
A | G | 1 | a0001c0002t0002g0179 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.775-948A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670568 | ||||||
chr1:230670619
|
T | A | 39 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0063others(36): Show | 52 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.775-897T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670619 | ||||||
chr1:230670629
|
C | G | 2 | a0001c0010t0001g0278a0001c0010t0001g0279 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.775-887C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670629 | ||||||
chr1:230670721
|
G | A | 1 | a0001c0002t0003g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.775-795G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670721 | ||||||
chr1:230670812
|
C | T | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.775-704C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670812 | ||||||
chr1:230670904
|
C | T | 1 | a0002c0003t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.775-612C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670904 | ||||||
chr1:230670952
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.775-564G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230670952 | ||||||
chr1:230671075
|
A | G | 1 | a0003c0004t0001g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.775-441A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671075 | ||||||
chr1:230671150
|
C | A | 1 | a0001c0002t0001g0062 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.775-366C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671150 | ||||||
chr1:230671164
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0084others(1): Show | 5 | HG02071.hp2 HG02129.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-352A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671164 | ||||||
chr1:230671319
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.775-197A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671319 | ||||||
chr1:230671486
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.775-30T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 7/17 | chr1 | 230671486 | ||||||
chr1:230671734
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.899+94G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671734 | ||||||
chr1:230671869
|
C | T | 2 | a0001c0001t0002g0197a0001c0001t0002g0210 | 2 | NA19058.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.899+229C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671869 | ||||||
chr1:230671946
|
A | G | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.899+306A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671946 | ||||||
chr1:230671980
|
T | G | 1 | a0001c0002t0004g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.899+340T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230671980 | ||||||
chr1:230672185
|
C | T | 1 | a0002c0003t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.899+545C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672185 | ||||||
chr1:230672254
|
G | A | 1 | a0001c0010t0001g0278 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.899+614G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672254 | ||||||
chr1:230672259
|
T | G | 163 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(160): Show | 215 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.899+619T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672259 | ||||||
chr1:230672303
|
G | A | 5 | a0001c0001t0001g0063a0001c0002t0001g0060a0001c0002t0003g0027others(2): Show | 6 | HG02071.hp1 NA18941.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.899+663G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672303 | ||||||
chr1:230672308
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0193 | 2 | HG02683.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.899+668A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672308 | ||||||
chr1:230672313
|
A | T | 1 | a0001c0002t0001g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.899+673A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672313 | ||||||
chr1:230672500
|
C | T | 39 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(36): Show | 51 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.899+860C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672500 | ||||||
chr1:230672552
|
C | T | 1 | a0001c0002t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.899+912C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672552 | ||||||
chr1:230672664
|
TA | T | 196 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(193): Show | 251 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.899+1037delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr1 | 230672664 | |||||
chr1:230672679
|
G | A | 198 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(195): Show | 253 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.899+1039G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672679 | ||||||
chr1:230672698
|
T | G | 1 | a0001c0002t0003g0076 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.899+1058T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672698 | ||||||
chr1:230672701
|
A | T | 1 | a0001c0001t0002g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.899+1061A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672701 | ||||||
chr1:230672812
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.899+1172T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672812 | ||||||
chr1:230672821
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.899+1181A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672821 | ||||||
chr1:230672890
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.899+1250G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672890 | ||||||
chr1:230672916
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.899+1276A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672916 | ||||||
chr1:230672922
|
C | T | 1 | a0001c0002t0001g0031 | 2 | HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.899+1282C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672922 | ||||||
chr1:230672966
|
T | A | 36 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(33): Show | 48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.899+1326T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672966 | ||||||
chr1:230672978
|
T | C | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.899+1338T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672978 | ||||||
chr1:230672998
|
G | T | 116 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0061others(113): Show | 152 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.899+1358G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230672998 | ||||||
chr1:230673169
|
C | T | 1 | a0001c0002t0004g0177 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.899+1529C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673169 | ||||||
chr1:230673457
|
G | A | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.900-1541G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673457 | ||||||
chr1:230673688
|
T | G | 32 | a0003c0004t0001g0051a0003c0004t0001g0178a0003c0004t0001g0257others(29): Show | 35 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.900-1310T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673688 | ||||||
chr1:230673799
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.900-1199A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673799 | ||||||
chr1:230673911
|
T | A | 1 | a0001c0018t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.900-1087T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673911 | ||||||
chr1:230673918
|
T | C | 1 | a0001c0014t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.900-1080T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673918 | ||||||
chr1:230673944
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.900-1054G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673944 | ||||||
chr1:230673969
|
A | G | 1 | a0001c0002t0004g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.900-1029A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230673969 | ||||||
chr1:230674112
|
A | G | 200 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(197): Show | 255 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.900-886A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674112 | ||||||
chr1:230674146
|
G | A | 1 | a0001c0002t0004g0152 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.900-852G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674146 | ||||||
chr1:230674225
|
T | C | 2 | a0001c0002t0004g0153a0001c0002t0004g0154 | 2 | HG00609.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.900-773T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674225 | ||||||
chr1:230674309
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.900-689G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674309 | ||||||
chr1:230674595
|
C | T | 2 | a0001c0001t0001g0127a0001c0010t0001g0278 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.900-403C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674595 | ||||||
chr1:230674616
|
G | T | 35 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(32): Show | 47 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.900-382G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674616 | ||||||
chr1:230674629
|
A | T | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(22): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.900-369A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674629 | ||||||
chr1:230674799
|
C | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0066 | 3 | HG01993.hp2 HG02735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.900-199C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674799 | ||||||
chr1:230674873
|
G | A | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.900-125G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 8/17 | chr1 | 230674873 | ||||||
chr1:230675138
|
C | T | 1 | a0010c0025t0001g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1026+14C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675138 | ||||||
chr1:230675215
|
G | C | 1 | a0002c0003t0001g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1026+91G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675215 | ||||||
chr1:230675321
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1026+197A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675321 | ||||||
chr1:230675389
|
T | C | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1026+265T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675389 | ||||||
chr1:230675731
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026+607C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675731 | ||||||
chr1:230675889
|
A | T | 1 | a0001c0002t0004g0126 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1026+765A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675889 | ||||||
chr1:230675970
|
G | A | 1 | a0001c0002t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1026+846G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230675970 | ||||||
chr1:230676142
|
T | G | 1 | a0001c0002t0002g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1026+1018T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676142 | ||||||
chr1:230676292
|
C | T | 275 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(272): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1026+1168C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676292 | ||||||
chr1:230676410
|
T | C | 239 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(236): Show | 306 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.1026+1286T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676410 | ||||||
chr1:230676436
|
C | T | 36 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(33): Show | 48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1026+1312C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676436 | ||||||
chr1:230676458
|
G | A | 4 | a0001c0001t0001g0127a0003c0004t0001g0129a0003c0004t0001g0305others(1): Show | 4 | HG02109.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+1334G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676458 | ||||||
chr1:230676520
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1026+1396G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676520 | ||||||
chr1:230676524
|
G | A | 1 | a0003c0004t0005g0274 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1026+1400G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676524 | ||||||
chr1:230676546
|
A | T | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1026+1422A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676546 | ||||||
chr1:230676583
|
C | T | 36 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(33): Show | 48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1026+1459C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676583 | ||||||
chr1:230676584
|
A | G | 307 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(304): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.1026+1460A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676584 | ||||||
chr1:230676587
|
A | C | 2 | a0001c0001t0001g0127a0001c0010t0001g0278 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1026+1463A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676587 | ||||||
chr1:230676700
|
T | C | 4 | a0001c0002t0003g0122a0001c0002t0003g0156a0001c0002t0003g0157others(1): Show | 4 | HG02083.hp2 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+1576T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676700 | ||||||
chr1:230676712
|
T | A | 163 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(160): Show | 215 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1026+1588T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676712 | ||||||
chr1:230676721
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1026+1597T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676721 | ||||||
chr1:230676729
|
T | C | 1 | a0001c0010t0001g0278 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026+1605T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676729 | ||||||
chr1:230676836
|
T | A | 2 | a0002c0003t0001g0106a0002c0003t0001g0114 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1026+1712T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676836 | ||||||
chr1:230676897
|
C | T | 3 | a0002c0005t0001g0011a0002c0005t0001g0038a0002c0005t0001g0113 | 6 | HG02027.hp2 NA18979.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+1773C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230676897 | ||||||
chr1:230677080
|
A | G | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(22): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1027-1833A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677080 | ||||||
chr1:230677089
|
T | G | 2 | a0001c0002t0003g0224a0001c0002t0003g0225 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1027-1824T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677089 | ||||||
chr1:230677315
|
C | T | 1 | a0002c0003t0001g0036 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1027-1598C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677315 | ||||||
chr1:230677344
|
G | C | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(22): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1027-1569G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677344 | ||||||
chr1:230677442
|
C | T | 1 | a0003c0004t0001g0272 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1027-1471C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677442 | ||||||
chr1:230677465
|
G | T | 1 | a0001c0002t0004g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1027-1448G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677465 | ||||||
chr1:230677533
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1027-1380A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677533 | ||||||
chr1:230677568
|
A | T | 36 | a0001c0001t0001g0063a0001c0001t0001g0069a0001c0001t0001g0079others(33): Show | 48 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1027-1345A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677568 | ||||||
chr1:230677587
|
GGCTTTAA others(16): Show |
G | 24 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(21): Show | 35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1315_1027-129 others(27): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr1 | 230677587 | |||||
chr1:230677637
|
C | T | 30 | a0003c0004t0001g0051a0003c0004t0001g0178a0003c0004t0001g0257others(27): Show | 33 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1027-1276C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677637 | ||||||
chr1:230677778
|
T | C | 4 | a0001c0002t0003g0122a0001c0002t0003g0156a0001c0002t0003g0157others(1): Show | 4 | HG02083.hp2 HG02165.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-1135T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677778 | ||||||
chr1:230677892
|
C | G | 24 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(21): Show | 35 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1027-1021C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677892 | ||||||
chr1:230677959
|
A | G | 1 | a0001c0002t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1027-954A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230677959 | ||||||
chr1:230678058
|
T | C | 2 | a0001c0012t0001g0090a0008c0011t0003g0089 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1027-855T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678058 | ||||||
chr1:230678092
|
A | G | 1 | a0001c0002t0001g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1027-821A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678092 | ||||||
chr1:230678190
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1027-723C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678190 | ||||||
chr1:230678235
|
C | T | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1027-678C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678235 | ||||||
chr1:230678297
|
T | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0119others(3): Show | 7 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1027-616T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678297 | ||||||
chr1:230678337
|
C | T | 234 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(231): Show | 300 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1027-576C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678337 | ||||||
chr1:230678346
|
C | T | 4 | a0001c0002t0004g0128a0001c0002t0004g0146a0001c0002t0004g0147others(1): Show | 4 | HG02135.hp2 NA18994.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-567C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678346 | ||||||
chr1:230678685
|
A | G | 25 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0218others(22): Show | 36 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1027-228A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678685 | ||||||
chr1:230678707
|
C | T | 2 | a0003c0004t0001g0129a0003c0004t0001g0305 | 2 | HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1027-206C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678707 | ||||||
chr1:230678884
|
A | G | 3 | a0003c0004t0001g0129a0003c0004t0001g0305a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1027-29A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 9/17 | chr1 | 230678884 | ||||||
chr1:230679070
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1166+18C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679070 | ||||||
chr1:230679082
|
G | A | 2 | a0001c0001t0001g0213a0010c0025t0001g0092 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1166+30G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679082 | ||||||
chr1:230679135
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1166+83C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679135 | ||||||
chr1:230679431
|
T | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0233a0001c0001t0001g0289others(28): Show | 49 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1166+379T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679431 | ||||||
chr1:230679438
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1166+386T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679438 | ||||||
chr1:230679451
|
G | A | 75 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0034others(72): Show | 106 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1166+399G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679451 | ||||||
chr1:230679459
|
T | G | 4 | a0001c0001t0002g0139a0001c0001t0002g0150a0001c0010t0001g0278others(1): Show | 4 | HG02055.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166+407T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679459 | ||||||
chr1:230679475
|
G | A | 2 | a0003c0004t0001g0129a0011c0027t0001g0241 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1166+423G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679475 | ||||||
chr1:230679630
|
T | C | 229 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(226): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1166+578T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679630 | ||||||
chr1:230679658
|
T | C | 1 | a0001c0001t0002g0184 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1166+606T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679658 | ||||||
chr1:230679670
|
C | A | 7 | a0001c0002t0004g0002a0001c0002t0004g0158a0001c0002t0004g0160others(4): Show | 13 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1166+618C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679670 | ||||||
chr1:230679735
|
T | G | 115 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0024others(112): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1166+683T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679735 | ||||||
chr1:230679799
|
C | T | 1 | a0001c0002t0003g0230 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1166+747C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679799 | ||||||
chr1:230679904
|
A | G | 2 | a0003c0004t0001g0051a0003c0004t0001g0263 | 3 | HG02615.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1166+852A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679904 | ||||||
chr1:230679991
|
A | G | 1 | a0004c0007t0003g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1166+939A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230679991 | ||||||
chr1:230680160
|
G | A | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1166+1108G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680160 | ||||||
chr1:230680377
|
G | GACCCTGG others(15): Show |
37 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(34): Show | 49 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1166+1329_1166+135 others(26): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230680377 | |||||
chr1:230680391
|
T | TGCAGCAT others(15): Show |
5 | a0001c0001t0001g0171a0001c0001t0001g0232a0001c0001t0002g0043others(2): Show | 6 | HG01168.hp2 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1166+1350_1166+135 others(26): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230680391 | |||||
chr1:230680438
|
T | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1166+1386T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680438 | ||||||
chr1:230680473
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1166+1421G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680473 | ||||||
chr1:230680495
|
C | T | 301 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(298): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1166+1443C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680495 | ||||||
chr1:230680511
|
C | G | 1 | a0001c0002t0004g0169 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1166+1459C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680511 | ||||||
chr1:230680523
|
C | T | 106 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(103): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1166+1471C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680523 | ||||||
chr1:230680651
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1166+1599C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680651 | ||||||
chr1:230680694
|
A | T | 29 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0031others(26): Show | 37 | HG00140.hp1 HG00423.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1166+1642A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680694 | ||||||
chr1:230680704
|
G | T | 1 | a0001c0002t0004g0167 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1166+1652G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680704 | ||||||
chr1:230680714
|
C | T | 124 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0031others(121): Show | 167 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1166+1662C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680714 | ||||||
chr1:230680811
|
T | C | 108 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(105): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1166+1759T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680811 | ||||||
chr1:230680849
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1166+1797G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680849 | ||||||
chr1:230680934
|
T | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166+1882T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680934 | ||||||
chr1:230680999
|
A | G | 128 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(125): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1166+1947A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230680999 | ||||||
chr1:230681105
|
C | T | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1166+2053C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681105 | ||||||
chr1:230681459
|
G | A | 3 | a0001c0001t0006g0115a0001c0001t0006g0118a0001c0021t0006g0116 | 3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1167-2115G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681459 | ||||||
chr1:230681609
|
T | G | 1 | a0001c0002t0003g0224 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1167-1965T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681609 | ||||||
chr1:230681638
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(166): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1167-1936G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681638 | ||||||
chr1:230681688
|
C | G | 127 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(124): Show | 170 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1167-1886C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681688 | ||||||
chr1:230681734
|
C | T | 52 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0044others(49): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1167-1840C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681734 | ||||||
chr1:230681900
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1167-1674C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230681900 | ||||||
chr1:230681983
|
TTATCATA others(2): Show |
T | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1167-1587_1167-157 others(13): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230681983 | |||||
chr1:230681984
|
TATC | T | 165 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(162): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1167-1587_1167-158 others(7): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230681984 | |||||
chr1:230682024
|
G | C | 295 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(292): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1167-1550G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682024 | ||||||
chr1:230682026
|
T | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0127a0001c0001t0001g0292others(9): Show | 16 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1167-1548T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682026 | ||||||
chr1:230682040
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0006g0118a0001c0021t0006g0116 | 3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1167-1534A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682040 | ||||||
chr1:230682113
|
T | G | 295 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(292): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1167-1461T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682113 | ||||||
chr1:230682342
|
C | G | 1 | a0009c0024t0001g0091 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1167-1232C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682342 | ||||||
chr1:230682524
|
A | G | 1 | a0001c0001t0002g0018 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1167-1050A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682524 | ||||||
chr1:230682558
|
G | A | 106 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(103): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1167-1016G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682558 | ||||||
chr1:230682643
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1167-931C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682643 | ||||||
chr1:230682665
|
G | A | 169 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(166): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1167-909G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682665 | ||||||
chr1:230682691
|
T | G | 3 | a0001c0001t0006g0115a0001c0001t0006g0118a0001c0021t0006g0116 | 3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1167-883T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682691 | ||||||
chr1:230682879
|
G | A | 106 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(103): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1167-695G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230682879 | ||||||
chr1:230683095
|
G | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1167-479G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230683095 | ||||||
chr1:230683125
|
T | G | 1 | a0001c0001t0007g0042 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1167-449T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | chr1 | 230683125 | ||||||
chr1:230683409
|
TA | T | 141 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(138): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1167-145delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230683409 | |||||
chr1:230683409
|
TAA | T | 32 | a0001c0001t0001g0044a0001c0001t0001g0079a0001c0001t0001g0239others(29): Show | 40 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1167-146_1167-145d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230683409 | |||||
chr1:230683549
|
ATTC | A | 121 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(118): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1167-16_1167-14del others(3): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr1 | 230683549 | |||||
chr1:230683733
|
G | GT | 285 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(282): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1228+110dupT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230683733 | |||||
chr1:230683733
|
G | GTT | 10 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(7): Show | 11 | HG01106.hp1 HG02615.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228+109_1228+110d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230683733 | |||||
chr1:230683846
|
C | A | 1 | a0003c0004t0001g0257 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1228+211C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230683846 | ||||||
chr1:230683896
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1228+261A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230683896 | ||||||
chr1:230683912
|
C | T | 1 | a0001c0014t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1228+277C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230683912 | ||||||
chr1:230684039
|
C | A | 1 | a0001c0002t0001g0281 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1228+404C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684039 | ||||||
chr1:230684039
|
C | G | 120 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(117): Show | 162 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1228+404C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684039 | ||||||
chr1:230684157
|
T | A | 1 | a0001c0014t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1228+522T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684157 | ||||||
chr1:230684264
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1228+629T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684264 | ||||||
chr1:230684275
|
A | G | 47 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(44): Show | 61 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1228+640A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684275 | ||||||
chr1:230684315
|
G | T | 2 | a0001c0002t0003g0226a0001c0002t0003g0227 | 2 | HG00673.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1228+680G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684315 | ||||||
chr1:230684476
|
T | G | 295 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(292): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1229-609T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684476 | ||||||
chr1:230684477
|
T | A | 295 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(292): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1229-608T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684477 | ||||||
chr1:230684546
|
A | C | 112 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(109): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1229-539A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684546 | ||||||
chr1:230684605
|
A | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1229-480A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684605 | ||||||
chr1:230684770
|
C | G | 1 | a0001c0002t0004g0242 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1229-315C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684770 | ||||||
chr1:230684832
|
G | A | 89 | a0001c0002t0001g0060a0001c0002t0003g0003a0001c0002t0003g0007others(86): Show | 123 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1229-253G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684832 | ||||||
chr1:230684859
|
G | T | 121 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(118): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1229-226G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684859 | ||||||
chr1:230684884
|
G | A | 124 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(121): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1229-201G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | chr1 | 230684884 | ||||||
chr1:230685017
|
C | CACATT | 47 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(44): Show | 61 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1229-66_1229-62dup others(5): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230685017 | |||||
chr1:230685034
|
TA | T | 112 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(109): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1229-47delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr1 | 230685034 | |||||
chr1:230685316
|
T | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 7 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380+80T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685316 | ||||||
chr1:230685437
|
T | C | 1 | a0001c0001t0002g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1380+201T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685437 | ||||||
chr1:230685451
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1380+215T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685451 | ||||||
chr1:230685474
|
G | T | 2 | a0001c0002t0003g0045a0001c0002t0004g0280 | 3 | NA18968.hp2 NA19009.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1380+238G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685474 | ||||||
chr1:230685570
|
T | C | 2 | a0001c0001t0002g0141a0001c0002t0004g0162 | 2 | HG02055.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1380+334T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685570 | ||||||
chr1:230685656
|
G | A | 121 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(118): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1380+420G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685656 | ||||||
chr1:230685738
|
T | C | 52 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0044others(49): Show | 69 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1380+502T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685738 | ||||||
chr1:230685827
|
G | A | 1 | a0002c0003t0001g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1380+591G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685827 | ||||||
chr1:230685833
|
C | T | 1 | a0001c0014t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1380+597C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685833 | ||||||
chr1:230685869
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+633G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685869 | ||||||
chr1:230685900
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+664G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230685900 | ||||||
chr1:230686014
|
T | C | 112 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0032others(109): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1380+778T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686014 | ||||||
chr1:230686026
|
A | G | 3 | a0001c0001t0006g0115a0001c0001t0006g0118a0001c0021t0006g0116 | 3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1380+790A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686026 | ||||||
chr1:230686041
|
A | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1380+805A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686041 | ||||||
chr1:230686166
|
T | C | 295 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(292): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1381-769T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686166 | ||||||
chr1:230686205
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1381-730G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686205 | ||||||
chr1:230686250
|
C | T | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1381-685C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686250 | ||||||
chr1:230686584
|
C | T | 121 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(118): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1381-351C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686584 | ||||||
chr1:230686601
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0284a0001c0001t0001g0291others(1): Show | 5 | HG02630.hp2 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-334A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686601 | ||||||
chr1:230686725
|
C | A | 295 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(292): Show | 388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1381-210C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686725 | ||||||
chr1:230686733
|
G | A | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-202G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686733 | ||||||
chr1:230686812
|
T | C | 1 | a0001c0002t0002g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1381-123T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686812 | ||||||
chr1:230686861
|
G | A | 174 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(171): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1381-74G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686861 | ||||||
chr1:230686886
|
A | C | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1381-49A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 12/17 | chr1 | 230686886 | ||||||
chr1:230687157
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0287a0001c0001t0001g0288 | 5 | HG00140.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+25C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687157 | ||||||
chr1:230687294
|
C | T | 174 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(171): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1578+162C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687294 | ||||||
chr1:230687318
|
A | G | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1578+186A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687318 | ||||||
chr1:230687342
|
T | A | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1578+210T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687342 | ||||||
chr1:230687391
|
C | T | 3 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0002g0198 | 3 | HG02258.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1578+259C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687391 | ||||||
chr1:230687560
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0284a0001c0001t0001g0291others(1): Show | 5 | HG02630.hp2 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+428C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687560 | ||||||
chr1:230687617
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0282 | 5 | HG01069.hp1 HG01175.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579-454A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687617 | ||||||
chr1:230687623
|
G | A | 1 | a0001c0001t0001g0054 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1579-448G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687623 | ||||||
chr1:230687632
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1579-439T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687632 | ||||||
chr1:230687697
|
TC | T | 90 | a0001c0002t0001g0060a0001c0002t0003g0003a0001c0002t0003g0007others(87): Show | 124 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1579-372delC | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr1 | 230687697 | |||||
chr1:230687724
|
T | C | 1 | a0003c0004t0001g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1579-347T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687724 | ||||||
chr1:230687738
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0001g0284a0001c0001t0001g0291others(1): Show | 5 | HG02630.hp2 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579-333T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230687738 | ||||||
chr1:230688006
|
T | A | 3 | a0001c0001t0006g0115a0001c0001t0006g0118a0001c0021t0006g0116 | 3 | HG02109.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1579-65T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230688006 | ||||||
chr1:230688047
|
A | G | 4 | a0004c0007t0003g0264a0004c0007t0003g0265a0004c0007t0003g0268others(1): Show | 4 | HG01261.hp1 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579-24A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 13/17 | chr1 | 230688047 | ||||||
chr1:230688201
|
C | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+58C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 14/17 | chr1 | 230688201 | ||||||
chr1:230688347
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02080.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1652-73G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 14/17 | chr1 | 230688347 | ||||||
chr1:230688643
|
G | A | 1 | a0001c0002t0004g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1794+81G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688643 | ||||||
chr1:230688835
|
G | C | 27 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0031others(24): Show | 35 | HG00140.hp1 HG00423.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1794+273G>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688835 | ||||||
chr1:230688881
|
G | A | 168 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(165): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1794+319G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688881 | ||||||
chr1:230688898
|
A | C | 1 | a0002c0003t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1794+336A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230688898 | ||||||
chr1:230689003
|
G | A | 4 | a0004c0007t0003g0264a0004c0007t0003g0265a0004c0007t0003g0268others(1): Show | 4 | HG01261.hp1 HG02622.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794+441G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689003 | ||||||
chr1:230689015
|
G | T | 2 | a0001c0010t0001g0278a0003c0004t0001g0129 | 2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1794+453G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689015 | ||||||
chr1:230689092
|
A | G | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1794+530A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689092 | ||||||
chr1:230689179
|
GTTTTTAT others(15): Show |
G | 1 | a0002c0003t0001g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1794+622_1794+643d others(24): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 230689179 | |||||
chr1:230689187
|
TAAAA | T | 63 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0046others(60): Show | 84 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1794+630_1794+633d others(6): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr1 | 230689187 | |||||
chr1:230689266
|
A | G | 121 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(118): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1794+704A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689266 | ||||||
chr1:230689651
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0117 | 3 | HG02258.hp2 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1795-363C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689651 | ||||||
chr1:230689681
|
T | G | 92 | a0001c0002t0001g0060a0001c0002t0001g0072a0001c0002t0001g0281others(89): Show | 126 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1795-333T>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689681 | ||||||
chr1:230689686
|
G | A | 1 | a0011c0027t0001g0241 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-328G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689686 | ||||||
chr1:230689701
|
T | C | 121 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0002t0001g0001others(118): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1795-313T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689701 | ||||||
chr1:230689722
|
G | A | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1795-292G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689722 | ||||||
chr1:230689754
|
C | T | 46 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0044others(43): Show | 58 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1795-260C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689754 | ||||||
chr1:230689899
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-115G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689899 | ||||||
chr1:230689944
|
T | A | 1 | a0001c0014t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1795-70T>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 15/17 | chr1 | 230689944 | ||||||
chr1:230690196
|
A | G | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1934+43A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690196 | ||||||
chr1:230690236
|
A | G | 2 | a0001c0002t0003g0231a0001c0002t0004g0153 | 2 | NA18985.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1934+83A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690236 | ||||||
chr1:230690429
|
C | G | 1 | a0003c0004t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1934+276C>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690429 | ||||||
chr1:230690577
|
C | T | 1 | a0001c0006t0001g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1934+424C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690577 | ||||||
chr1:230690915
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1935-469G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690915 | ||||||
chr1:230690952
|
A | C | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1935-432A>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230690952 | ||||||
chr1:230691160
|
CAT | C | 16 | a0001c0001t0001g0046a0001c0001t0002g0017a0001c0001t0002g0019others(13): Show | 25 | HG00544.hp1 HG00597.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.1935-221_1935-220d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691160 | |||||
chr1:230691177
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1935-207A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230691177 | ||||||
chr1:230691178
|
T | TATATATA others(27): Show |
3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0014t0001g0093 | 3 | HG02080.hp1 HG03139.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1935-199_1935-198i others(36): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691178 | |||||
chr1:230691189
|
G | GTATATAC others(27): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0291a0001c0001t0001g0296 | 4 | HG02630.hp2 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935-163_1935-162i others(36): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691189 | |||||
chr1:230691189
|
G | GTATATAC others(61): Show |
1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1935-163_1935-162i others(70): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691189 | |||||
chr1:230691197
|
A | G | 1 | a0001c0014t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1935-187A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | chr1 | 230691197 | ||||||
chr1:230691250
|
T | TA | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0014t0001g0093 | 3 | HG02080.hp1 HG03139.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1935-133dupA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr1 | 230691250 | |||||
chr1:230691841
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0001g0054a0003c0004t0001g0257others(1): Show | 7 | HG00741.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2115+277A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230691841 | ||||||
chr1:230691887
|
C | T | 3 | a0001c0010t0001g0278a0003c0004t0001g0129a0011c0027t0001g0241 | 3 | HG02109.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2115+323C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230691887 | ||||||
chr1:230692208
|
G | T | 1 | a0001c0002t0004g0166 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2115+644G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692208 | ||||||
chr1:230692227
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2115+663C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692227 | ||||||
chr1:230692231
|
G | A | 1 | a0003c0004t0001g0305 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2115+667G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692231 | ||||||
chr1:230692352
|
GA | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0284others(15): Show | 22 | HG01106.hp1 HG01243.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.2115+800delA | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230692352 | |||||
chr1:230692486
|
A | T | 2 | a0003c0004t0001g0051a0003c0004t0001g0263 | 3 | HG02615.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2116-806A>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692486 | ||||||
chr1:230692553
|
G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0031others(25): Show | 36 | HG00140.hp1 HG00423.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2116-739G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692553 | ||||||
chr1:230692602
|
G | T | 200 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0034others(197): Show | 268 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.2116-690G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692602 | ||||||
chr1:230692613
|
T | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(89): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2116-679T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692613 | ||||||
chr1:230692641
|
G | A | 290 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(287): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.2116-651G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692641 | ||||||
chr1:230692645
|
A | G | 147 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(144): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2116-647A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692645 | ||||||
chr1:230692692
|
A | G | 140 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0127others(137): Show | 187 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.2116-600A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692692 | ||||||
chr1:230692727
|
CTG | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2116-562_2116-561d others(4): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230692727 | |||||
chr1:230692759
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2116-533C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692759 | ||||||
chr1:230692789
|
GTTA | G | 154 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(151): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.2116-500_2116-498d others(5): Show |
COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230692789 | |||||
chr1:230692792
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0236a0001c0001t0007g0042others(3): Show | 7 | HG01433.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2116-500A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692792 | ||||||
chr1:230692918
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0002g0138others(7): Show | 13 | HG01106.hp1 HG01243.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2116-374A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230692918 | ||||||
chr1:230693014
|
A | G | 135 | a0001c0001t0001g0023a0001c0001t0001g0052a0001c0001t0001g0284others(132): Show | 181 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.2116-278A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693014 | ||||||
chr1:230693019
|
G | T | 292 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0022others(289): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.2116-273G>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693019 | ||||||
chr1:230693127
|
A | G | 118 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0031others(115): Show | 160 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.2116-165A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693127 | ||||||
chr1:230693225
|
CT | C | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2116-59delT | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr1 | 230693225 | |||||
chr1:230693227
|
T | C | 6 | a0001c0006t0001g0047a0001c0006t0001g0048a0001c0006t0001g0243others(3): Show | 7 | HG01109.hp1 HG02280.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2116-65T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693227 | ||||||
chr1:230693233
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0007g0042 | 3 | HG02717.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2116-59T>C | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693233 | ||||||
chr1:230693235
|
C | T | 1 | a0001c0001t0007g0042 | 2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2116-57C>T | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693235 | ||||||
chr1:230693241
|
C | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2116-51C>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693241 | ||||||
chr1:230693279
|
A | G | 1 | a0001c0020t0004g0203 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2116-13A>G | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693279 | ||||||
chr1:230693282
|
G | A | 1 | a0001c0002t0004g0280 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2116-10G>A | COG2 | ENSG00000135775.14 | transcript | ENST00000366669.9 | protein_coding | 17/17 | chr1 | 230693282 |