geneid | 1368 |
---|---|
ensemblid | ENSG00000135678.12 |
hgncid | 2311 |
symbol | CPM |
name | carboxypeptidase M |
refseq_nuc | NM_198320.5 |
refseq_prot | NP_938079.1 |
ensembl_nuc | ENST00000551568.6 |
ensembl_prot | ENSP00000448517.1 |
mane_status | MANE Select |
chr | chr12 |
start | 68851175 |
end | 68933171 |
strand | - |
ver | v1.2 |
region | chr12:68851175-68933171 |
region5000 | chr12:68846175-68938171 |
regionname0 | CPM_chr12_68851175_68933171 |
regionname5000 | CPM_chr12_68846175_68938171 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 443 | 278 | 37 | 53 | 139 | 12 | 35 | 99 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002 | 0/0 | 443 | 56 | 51 | 2 | 1 | 0 | 2 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0003 | 0/0 | 443 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0004 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0005 | 0/0 | 443 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0006 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0007 | 0/0 | 443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1332 | 116 | 16 | 17 | 65 | 7 | 10 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0002 | 1/0 | 1332 | 114 | 8 | 16 | 73 | 3 | 13 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0003 | 0/0 | 1332 | 26 | 24 | 1 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0004 | 0/0 | 1332 | 20 | 6 | 10 | 1 | 0 | 3 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0005 | 0/0 | 1332 | 17 | 17 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0006 | 0/0 | 1332 | 15 | 7 | 5 | 0 | 0 | 3 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0007 | 0/0 | 1332 | 12 | 0 | 4 | 0 | 2 | 6 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0008 | 0/0 | 1332 | 6 | 5 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0009 | 0/0 | 1332 | 4 | 3 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0010 | 0/0 | 1332 | 3 | 2 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0011 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0012 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0013 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0014 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0015 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0016 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
c0017 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5296 | 166 | 7 | 25 | 108 | 3 | 23 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0002 | 0/0 | 5296 | 22 | 6 | 7 | 4 | 3 | 2 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0003 | 0/0 | 5296 | 17 | 5 | 4 | 1 | 3 | 4 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0004 | 0/0 | 5297 | 11 | 11 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0005 | 0/0 | 5298 | 9 | 1 | 6 | 0 | 0 | 2 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0006 | 0/0 | 5297 | 7 | 1 | 0 | 5 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0007 | 0/0 | 5295 | 7 | 7 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0008 | 0/0 | 5295 | 6 | 5 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0009 | 0/0 | 5296 | 6 | 0 | 4 | 1 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0010 | 0/0 | 5296 | 6 | 0 | 0 | 6 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0011 | 0/0 | 5298 | 5 | 1 | 2 | 0 | 0 | 2 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0012 | 0/0 | 5294 | 5 | 5 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0013 | 0/0 | 5298 | 3 | 3 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0014 | 0/0 | 5297 | 3 | 0 | 0 | 2 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0015 | 0/0 | 5301 | 3 | 3 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0016 | 0/0 | 5297 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0017 | 0/0 | 5294 | 2 | 1 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0018 | 0/0 | 5292 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0019 | 0/0 | 5296 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0020 | 0/0 | 5294 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0021 | 0/0 | 5276 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0022 | 0/0 | 5296 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0023 | 0/0 | 5293 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0024 | 0/0 | 5296 | 2 | 0 | 0 | 0 | 1 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0025 | 0/0 | 5292 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0026 | 0/0 | 5297 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0027 | 0/0 | 5299 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0028 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0029 | 0/0 | 5292 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0030 | 0/0 | 5291 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0031 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0032 | 0/0 | 5298 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0033 | 0/0 | 5300 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0034 | 0/0 | 5300 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0035 | 0/0 | 5299 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0036 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0037 | 0/0 | 5298 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0038 | 0/0 | 5298 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0039 | 0/0 | 5298 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0040 | 0/0 | 5294 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0041 | 0/0 | 5294 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0042 | 0/0 | 5297 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0043 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0044 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0045 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0046 | 0/0 | 5295 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0047 | 0/0 | 4415 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0048 | 0/0 | 5298 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0049 | 1/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0050 | 0/0 | 5297 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0051 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0052 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0053 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0054 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0055 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0056 | 0/1 | 5296 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0057 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0058 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0059 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0060 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0061 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0062 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0063 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0064 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0065 | 0/0 | 5293 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0066 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0067 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
t0068 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1332 | 116 | 16 | 17 | 65 | 7 | 10 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002 | 1/0 | 1332 | 114 | 8 | 16 | 73 | 3 | 13 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004 | 0/0 | 1332 | 20 | 6 | 10 | 1 | 0 | 3 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006 | 0/0 | 1332 | 15 | 7 | 5 | 0 | 0 | 3 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007 | 0/0 | 1332 | 12 | 0 | 4 | 0 | 2 | 6 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0016 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003 | 0/0 | 1332 | 26 | 24 | 1 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005 | 0/0 | 1332 | 17 | 17 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0008 | 0/0 | 1332 | 6 | 5 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0009 | 0/0 | 1332 | 4 | 3 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0010 | 0/0 | 1332 | 3 | 2 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0003c0011 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0003c0012 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0004c0013 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0005c0014 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0006c0015 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0007c0017 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6627 | 80 | 6 | 14 | 51 | 1 | 8 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0002 | 0/0 | 6627 | 6 | 0 | 1 | 3 | 2 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0003 | 0/0 | 6627 | 3 | 0 | 1 | 0 | 1 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0004 | 0/0 | 6628 | 4 | 4 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0006 | 0/0 | 6628 | 3 | 0 | 0 | 3 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0009 | 0/0 | 6627 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0010 | 0/0 | 6627 | 2 | 0 | 0 | 2 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0014 | 0/0 | 6628 | 3 | 0 | 0 | 2 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0018 | 0/0 | 6623 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0024 | 0/0 | 6627 | 2 | 0 | 0 | 0 | 1 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0026 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0051 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0052 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0053 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0055 | 0/0 | 6627 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0056 | 0/1 | 6627 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0058 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0059 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0066 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0001t0067 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0001 | 0/0 | 6627 | 79 | 1 | 10 | 56 | 1 | 11 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0002 | 0/0 | 6627 | 4 | 0 | 1 | 1 | 1 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0003 | 0/0 | 6627 | 5 | 0 | 3 | 1 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0004 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0006 | 0/0 | 6628 | 4 | 1 | 0 | 2 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0007 | 0/0 | 6626 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0009 | 0/0 | 6627 | 2 | 0 | 1 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0010 | 0/0 | 6627 | 4 | 0 | 0 | 4 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0031 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0043 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0048 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0049 | 1/0 | 6627 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0050 | 0/0 | 6628 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0054 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0060 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0061 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0062 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0063 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0064 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0065 | 0/0 | 6624 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0002t0068 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0002 | 0/0 | 6627 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0005 | 0/0 | 6629 | 7 | 0 | 6 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0008 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0011 | 0/0 | 6629 | 4 | 1 | 1 | 0 | 0 | 2 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0012 | 0/0 | 6625 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0017 | 0/0 | 6625 | 2 | 1 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0020 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0036 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0004t0038 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0002 | 0/0 | 6627 | 4 | 0 | 4 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0005 | 0/0 | 6629 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0008 | 0/0 | 6626 | 4 | 4 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0012 | 0/0 | 6625 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0037 | 0/0 | 6629 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0039 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0040 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0006t0047 | 0/0 | 5746 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007t0001 | 0/0 | 6627 | 2 | 0 | 0 | 0 | 1 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007t0002 | 0/0 | 6627 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007t0003 | 0/0 | 6627 | 4 | 0 | 0 | 0 | 1 | 3 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007t0009 | 0/0 | 6627 | 3 | 0 | 3 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007t0042 | 0/0 | 6628 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0007t0045 | 0/0 | 6627 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0001c0016t0011 | 0/0 | 6629 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0001 | 0/0 | 6627 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0003 | 0/0 | 6627 | 5 | 5 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0004 | 0/0 | 6628 | 3 | 3 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0007 | 0/0 | 6626 | 4 | 4 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0015 | 0/0 | 6632 | 3 | 3 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0019 | 0/0 | 6627 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0025 | 0/0 | 6623 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0026 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0027 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0028 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0029 | 0/0 | 6623 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0030 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0032 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0033 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0003t0057 | 0/0 | 6627 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0002 | 0/0 | 6627 | 3 | 3 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0005 | 0/0 | 6629 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0013 | 0/0 | 6629 | 3 | 3 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0016 | 0/0 | 6628 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0020 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0021 | 0/0 | 6607 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0022 | 0/0 | 6627 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0023 | 0/0 | 6624 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0005t0035 | 0/0 | 6630 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0008t0001 | 0/0 | 6627 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0008t0004 | 0/0 | 6628 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0008t0019 | 0/0 | 6627 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0008t0025 | 0/0 | 6623 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0008t0034 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0009t0001 | 0/0 | 6627 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0009t0002 | 0/0 | 6627 | 2 | 2 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0009t0044 | 0/0 | 6627 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0010t0002 | 0/0 | 6627 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0010t0008 | 0/0 | 6626 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0002c0010t0046 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0003c0011t0012 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0003c0012t0007 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0004c0013t0004 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0005c0014t0001 | 0/0 | 6627 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0006c0015t0041 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
a0007c0017t0001 | 0/0 | 6627 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | copy fasta | chr12 | 68846175 | 68938171 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0009g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0014g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0014g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0014g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0018g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0024g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0024g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0026g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0051g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0052g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0053g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0055g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0056g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0058g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0059g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0066g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0001t0067g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0006g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0009g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0010g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0010g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0031g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0043g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0048g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0049g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0050g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0054g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0060g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0061g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0062g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0063g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0064g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0065g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0002t0068g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0011g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0011g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0011g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0011g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0017g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0017g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0020g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0036g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0004t0038g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0012g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0037g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0039g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0040g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0006t0047g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0009g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0042g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0007t0045g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0001c0016t0011g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0015g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0015g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0015g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0025g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0026g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0027g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0028g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0029g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0030g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0032g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0033g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0003t0057g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0016g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0020g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0021g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0021g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0022g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0022g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0023g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0023g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0005t0035g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0008t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0008t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0008t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0008t0019g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0008t0025g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0008t0034g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0009t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0009t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0009t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0009t0044g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0010t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0010t0008g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0002c0010t0046g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0003c0011t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0003c0012t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0004c0013t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0005c0014t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0006c0015t0041g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
a0007c0017t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0024 | g0220 | EUR | GBR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00099 | hp2 | a0001 | c0007 | t0003 | g0147 | EUR | GBR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00140 | hp1 | a0001 | c0001 | t0009 | g0235 | EUR | GBR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0146 | EUR | GBR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0278 | EUR | FIN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00544 | hp2 | a0001 | c0001 | t0051 | g0067 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00558 | hp2 | a0001 | c0002 | t0009 | g0113 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00621 | hp2 | a0001 | c0002 | t0063 | g0181 | EAS | CHS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00639 | hp1 | a0002 | c0003 | t0029 | g0018 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0276 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00642 | hp2 | a0001 | c0004 | t0005 | g0145 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00733 | hp1 | a0001 | c0001 | t0055 | g0305 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00733 | hp2 | a0001 | c0004 | t0038 | g0275 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00741 | hp1 | a0001 | c0006 | t0039 | g0182 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01071 | hp2 | a0001 | c0004 | t0011 | g0056 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01074 | hp1 | a0001 | c0004 | t0005 | g0148 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01081 | hp1 | a0001 | c0004 | t0005 | g0154 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01081 | hp2 | a0001 | c0016 | t0011 | g0127 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01106 | hp1 | a0001 | c0002 | t0009 | g0057 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01109 | hp1 | a0001 | c0007 | t0009 | g0077 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01109 | hp2 | a0001 | c0002 | t0048 | g0287 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01167 | hp1 | a0002 | c0010 | t0008 | g0025 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01167 | hp2 | a0001 | c0004 | t0005 | g0279 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01169 | hp2 | a0001 | c0004 | t0005 | g0273 | AMR | PUR | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01258 | hp2 | a0001 | c0006 | t0002 | g0002 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0272 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01346 | hp2 | a0001 | c0007 | t0009 | g0075 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01358 | hp1 | a0001 | c0004 | t0002 | g0038 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01358 | hp2 | a0001 | c0007 | t0009 | g0076 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01361 | hp2 | a0001 | c0004 | t0017 | g0102 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01433 | hp1 | a0007 | c0017 | t0001 | g0055 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01516 | hp1 | a0001 | c0007 | t0001 | g0132 | EUR | IBS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | IBS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01517 | hp1 | a0001 | c0001 | t0014 | g0227 | EUR | IBS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01891 | hp1 | a0001 | c0004 | t0011 | g0218 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01891 | hp2 | a0002 | c0003 | t0007 | g0320 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01952 | hp2 | a0001 | c0006 | t0002 | g0002 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01993 | hp2 | a0001 | c0006 | t0002 | g0141 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02004 | hp2 | a0001 | c0007 | t0045 | g0268 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02055 | hp1 | a0001 | c0001 | t0053 | g0243 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02055 | hp2 | a0001 | c0002 | t0031 | g0050 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02083 | hp1 | a0001 | c0002 | t0064 | g0101 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02083 | hp2 | a0001 | c0002 | t0006 | g0063 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02145 | hp1 | a0002 | c0005 | t0002 | g0309 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02145 | hp2 | a0002 | c0003 | t0003 | g0015 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02148 | hp2 | a0001 | c0006 | t0002 | g0302 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | CDX | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CDX | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | CDX | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02257 | hp2 | a0001 | c0006 | t0008 | g0282 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02258 | hp1 | a0001 | c0002 | t0006 | g0285 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02258 | hp2 | a0002 | c0003 | t0057 | g0008 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0036 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02280 | hp1 | a0002 | c0003 | t0007 | g0317 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02280 | hp2 | a0002 | c0010 | t0046 | g0029 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02451 | hp1 | a0002 | c0003 | t0030 | g0030 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02451 | hp2 | a0001 | c0001 | t0026 | g0231 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | KHV | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02572 | hp1 | a0001 | c0006 | t0012 | g0225 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02572 | hp2 | a0002 | c0008 | t0004 | g0020 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02602 | hp1 | a0005 | c0014 | t0001 | g0337 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02615 | hp1 | a0002 | c0003 | t0004 | g0314 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02615 | hp2 | a0001 | c0006 | t0008 | g0226 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02622 | hp1 | a0002 | c0003 | t0007 | g0322 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02622 | hp2 | a0001 | c0002 | t0004 | g0246 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02630 | hp1 | a0002 | c0005 | t0023 | g0011 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02630 | hp2 | a0002 | c0003 | t0026 | g0319 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02647 | hp1 | a0001 | c0001 | t0066 | g0256 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02683 | hp2 | a0001 | c0004 | t0011 | g0209 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02717 | hp1 | a0002 | c0005 | t0020 | g0316 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02717 | hp2 | a0002 | c0003 | t0015 | g0329 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02723 | hp1 | a0002 | c0005 | t0021 | g0333 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02723 | hp2 | a0002 | c0003 | t0019 | g0026 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02735 | hp1 | a0001 | c0007 | t0001 | g0124 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0086 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02738 | hp1 | a0001 | c0006 | t0005 | g0296 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02809 | hp1 | a0002 | c0003 | t0003 | g0033 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02809 | hp2 | a0002 | c0005 | t0022 | g0326 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02818 | hp1 | a0002 | c0005 | t0021 | g0331 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02818 | hp2 | a0002 | c0003 | t0007 | g0324 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02886 | hp1 | a0002 | c0008 | t0025 | g0024 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02886 | hp2 | a0001 | c0004 | t0017 | g0103 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02895 | hp1 | a0002 | c0005 | t0016 | g0004 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02895 | hp2 | a0002 | c0003 | t0004 | g0019 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02896 | hp2 | a0002 | c0005 | t0013 | g0009 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02897 | hp1 | a0002 | c0005 | t0013 | g0010 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02897 | hp2 | a0002 | c0005 | t0016 | g0003 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02922 | hp1 | a0002 | c0003 | t0033 | g0336 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02970 | hp1 | a0002 | c0008 | t0034 | g0327 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02970 | hp2 | a0001 | c0002 | t0007 | g0247 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02976 | hp1 | a0002 | c0003 | t0003 | g0016 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02976 | hp2 | a0002 | c0010 | t0002 | g0022 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03041 | hp1 | a0002 | c0005 | t0013 | g0013 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03041 | hp2 | a0002 | c0008 | t0019 | g0325 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03098 | hp1 | a0002 | c0009 | t0002 | g0032 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03098 | hp2 | a0001 | c0006 | t0008 | g0244 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03130 | hp1 | a0002 | c0003 | t0027 | g0005 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03130 | hp2 | a0004 | c0013 | t0004 | g0027 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03139 | hp1 | a0001 | c0002 | t0065 | g0111 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03139 | hp2 | a0001 | c0006 | t0012 | g0241 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03209 | hp1 | a0002 | c0003 | t0003 | g0328 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03225 | hp1 | a0001 | c0006 | t0008 | g0245 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03225 | hp2 | a0002 | c0003 | t0015 | g0332 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03239 | hp1 | a0002 | c0003 | t0001 | g0313 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03453 | hp1 | a0002 | c0005 | t0035 | g0017 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03453 | hp2 | a0001 | c0004 | t0020 | g0069 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03486 | hp2 | a0002 | c0003 | t0032 | g0335 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03490 | hp1 | a0001 | c0004 | t0005 | g0149 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03490 | hp2 | a0002 | c0008 | t0001 | g0312 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03491 | hp1 | a0001 | c0001 | t0024 | g0216 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03516 | hp1 | a0002 | c0005 | t0005 | g0014 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03516 | hp2 | a0001 | c0001 | t0018 | g0228 | AFR | ESN | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03540 | hp1 | a0003 | c0011 | t0012 | g0028 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03540 | hp2 | a0006 | c0015 | t0041 | g0301 | AFR | GWD | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03579 | hp1 | a0001 | c0002 | t0068 | g0299 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03579 | hp2 | a0002 | c0005 | t0002 | g0310 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03669 | hp1 | a0001 | c0006 | t0037 | g0224 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03669 | hp2 | a0001 | c0004 | t0011 | g0058 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03688 | hp2 | a0001 | c0007 | t0002 | g0051 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03710 | hp2 | a0001 | c0007 | t0003 | g0126 | SAS | PJL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03927 | hp1 | a0001 | c0007 | t0003 | g0123 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04115 | hp1 | a0001 | c0002 | t0006 | g0286 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0258 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | BEB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04199 | hp1 | a0001 | c0007 | t0042 | g0078 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | STU | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18906 | hp1 | a0002 | c0009 | t0002 | g0031 | AFR | YRI | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18906 | hp2 | a0002 | c0005 | t0002 | g0323 | AFR | YRI | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18939 | hp1 | a0001 | c0001 | t0014 | g0291 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18949 | hp1 | a0001 | c0001 | t0010 | g0136 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18954 | hp1 | a0001 | c0002 | t0060 | g0100 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18960 | hp1 | a0001 | c0002 | t0010 | g0293 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18968 | hp1 | a0001 | c0002 | t0062 | g0280 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18971 | hp2 | a0001 | c0002 | t0010 | g0292 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18991 | hp2 | a0001 | c0002 | t0010 | g0093 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18993 | hp1 | a0001 | c0001 | t0006 | g0259 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18993 | hp2 | a0001 | c0002 | t0006 | g0089 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19000 | hp1 | a0001 | c0001 | t0014 | g0118 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19006 | hp1 | a0001 | c0002 | t0050 | g0092 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19009 | hp2 | a0001 | c0001 | t0059 | g0289 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19030 | hp1 | a0001 | c0004 | t0008 | g0233 | AFR | LWK | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19030 | hp2 | a0001 | c0001 | t0067 | g0083 | AFR | LWK | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0315 | AFR | LWK | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19043 | hp2 | a0002 | c0003 | t0004 | g0023 | AFR | LWK | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19062 | hp2 | a0001 | c0004 | t0036 | g0253 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19063 | hp2 | a0001 | c0002 | t0043 | g0087 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19066 | hp1 | a0001 | c0002 | t0010 | g0187 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19070 | hp1 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19072 | hp2 | a0002 | c0009 | t0001 | g0311 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19079 | hp2 | a0001 | c0001 | t0052 | g0054 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19083 | hp2 | a0001 | c0002 | t0061 | g0046 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19084 | hp2 | a0001 | c0002 | t0054 | g0175 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19086 | hp1 | a0001 | c0001 | t0058 | g0214 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19240 | hp1 | a0001 | c0004 | t0012 | g0300 | AFR | YRI | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA19240 | hp2 | a0001 | c0002 | t0007 | g0095 | AFR | YRI | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20129 | hp1 | a0001 | c0001 | t0018 | g0232 | AFR | ASW | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | ASW | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0266 | EUR | TSI | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0239 | EUR | TSI | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20905 | hp1 | a0001 | c0007 | t0003 | g0085 | SAS | GIH | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20905 | hp2 | a0001 | c0006 | t0047 | g0211 | SAS | GIH | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG01123 | hp2 | a0001 | c0004 | t0005 | g0061 | AMR | CLM | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02109 | hp1 | a0001 | c0004 | t0012 | g0162 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02109 | hp2 | a0002 | c0008 | t0004 | g0321 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02486 | hp1 | a0002 | c0005 | t0023 | g0012 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02486 | hp2 | a0002 | c0009 | t0044 | g0021 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02559 | hp1 | a0002 | c0003 | t0028 | g0006 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG02559 | hp2 | a0002 | c0005 | t0022 | g0318 | AFR | ACB | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03471 | hp1 | a0002 | c0003 | t0025 | g0007 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG03471 | hp2 | a0001 | c0006 | t0040 | g0242 | AFR | MSL | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG06807 | hp1 | a0003 | c0012 | t0007 | g0334 | AFR | USA | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | USA | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20300 | hp1 | a0002 | c0003 | t0015 | g0330 | AFR | USA | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0056 | g0196 | REF | REF | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0049 | g0274 | REF | REF | CPM_chr12_68846175_68938171 | CPM | chr12 | 68846175 | 68938171 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68866912
|
T | C | 1 | a0004 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.924A>G | p.Ile308Met | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/9 | 957/6627 | 924/1332 | 308/443 | chr12 | 68866912 | ||
chr12:68871818
|
C | T | 3 | a0003a0004a0006 | 4 | HG03130.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
missense_variant | MODERATE | c.397G>A | p.Val133Ile | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/9 | 430/6627 | 397/1332 | 133/443 | chr12 | 68871818 | ||
chr12:68871873
|
G | C | 1 | a0007 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.342C>G | p.Ile114Met | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/9 | 375/6627 | 342/1332 | 114/443 | chr12 | 68871873 | ||
chr12:68932728
|
T | C | 1 | a0005 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.110A>G | p.Gln37Arg | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/9 | 143/6627 | 110/1332 | 37/443 | chr12 | 68932728 | ||
chr12:68932767
|
C | T | 4 | a0002a0003a0004others(1): Show | 60 | HG00639.hp1 HG01167.hp1 HG01891.hp2 others(57): Show |
missense_variant | MODERATE | c.71G>A | p.Arg24His | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/9 | 104/6627 | 71/1332 | 24/443 | chr12 | 68932767 | ||
chr12:68933144
|
G | T | 1 | a0002 | 1 | HG02559.hp1 | splice_region_variant | LOW | c.-6C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 1/9 | chr12 | 68933144 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68858935
|
A | G | 7 | a0001c0004a0001c0006a0001c0016others(4): Show | 58 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(55): Show |
synonymous_variant | LOW | c.1077T>C | p.Ser359Ser | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/9 | 1110/6627 | 1077/1332 | 359/443 | chr12 | 68858935 | ||
chr12:68866999
|
C | T | 3 | a0001c0007a0001c0016a0002c0009 | 17 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(14): Show |
synonymous_variant | LOW | c.837G>A | p.Thr279Thr | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/9 | 870/6627 | 837/1332 | 279/443 | chr12 | 68866999 | ||
chr12:68871798
|
A | G | 5 | a0001c0001a0001c0006a0002c0008others(2): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
synonymous_variant | LOW | c.417T>C | p.Tyr139Tyr | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/9 | 450/6627 | 417/1332 | 139/443 | chr12 | 68871798 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68851384
|
G | A | 2 | a0002c0003t0019a0002c0008t0019 | 2 | HG02723.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5053C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 5053 | chr12 | 68851384 | |||||
chr12:68851435
|
C | T | 1 | a0001c0001t0051 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5002G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 5002 | chr12 | 68851435 | |||||
chr12:68851453
|
T | C | 29 | a0001c0001t0026a0001c0001t0067a0001c0002t0007others(26): Show | 41 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4984A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4984 | chr12 | 68851453 | |||||
chr12:68851467
|
C | T | 1 | a0002c0008t0034 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4970G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4970 | chr12 | 68851467 | |||||
chr12:68851468
|
G | A | 1 | a0001c0001t0058 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4969C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4969 | chr12 | 68851468 | |||||
chr12:68851536
|
G | A | 1 | a0002c0005t0022 | 2 | HG02559.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4901C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4901 | chr12 | 68851536 | |||||
chr12:68851543
|
AG | A | 4 | a0001c0002t0031a0002c0003t0025a0002c0003t0030others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4893delC | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4893 | chr12 | 68851543 | |||||
chr12:68851610
|
C | CA | 7 | a0001c0001t0014a0001c0002t0048a0001c0004t0017others(4): Show | 10 | HG01109.hp2 HG01361.hp2 HG01517.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4826dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4826 | chr12 | 68851610 | |||||
chr12:68851610
|
C | CAA | 15 | a0001c0002t0007a0001c0004t0008a0001c0004t0012others(12): Show | 24 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4825_*4826dupTT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4826 | chr12 | 68851610 | |||||
chr12:68851625
|
G | A | 1 | a0001c0004t0036 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4812C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4812 | chr12 | 68851625 | |||||
chr12:68851859
|
T | C | 1 | a0001c0002t0060 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4578A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4578 | chr12 | 68851859 | |||||
chr12:68851977
|
G | A | 2 | a0001c0001t0067a0001c0002t0048 | 2 | HG01109.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4460C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4460 | chr12 | 68851977 | |||||
chr12:68852074
|
G | A | 1 | a0002c0005t0023 | 2 | HG02486.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4363C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4363 | chr12 | 68852074 | |||||
chr12:68852185
|
A | G | 92 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(89): Show | 310 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*4252T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4252 | chr12 | 68852185 | |||||
chr12:68852185
|
A | T | 3 | a0001c0001t0066a0001c0002t0068a0002c0005t0021 | 4 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4252T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4252 | chr12 | 68852185 | |||||
chr12:68852314
|
A | G | 1 | a0002c0003t0057 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4123T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 4123 | chr12 | 68852314 | |||||
chr12:68852446
|
G | C | 1 | a0001c0001t0018 | 2 | HG03516.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3991C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3991 | chr12 | 68852446 | |||||
chr12:68852537
|
TTTTC | T | 22 | a0001c0001t0018a0001c0002t0007a0001c0002t0065others(19): Show | 34 | HG00639.hp1 HG01167.hp1 HG01361.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3896_*3899delGAAA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3896 | chr12 | 68852537 | |||||
chr12:68852548
|
T | C | 2 | a0001c0002t0048a0002c0005t0021 | 3 | HG01109.hp2 HG02723.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3889A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3889 | chr12 | 68852548 | |||||
chr12:68852549
|
C | T | 1 | a0002c0005t0021 | 2 | HG02723.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3888G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3888 | chr12 | 68852549 | |||||
chr12:68852551
|
T | C | 1 | a0002c0005t0021 | 2 | HG02723.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3886A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3886 | chr12 | 68852551 | |||||
chr12:68852556
|
C | CT | 19 | a0001c0001t0006a0001c0001t0051a0001c0001t0052others(16): Show | 35 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3880dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3880 | chr12 | 68852556 | |||||
chr12:68852556
|
C | T | 1 | a0002c0005t0021 | 2 | HG02723.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3881G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3881 | chr12 | 68852556 | |||||
chr12:68852583
|
G | A | 1 | a0001c0002t0043 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3854C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3854 | chr12 | 68852583 | |||||
chr12:68852603
|
G | A | 1 | a0001c0002t0061 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3834C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3834 | chr12 | 68852603 | |||||
chr12:68852704
|
C | G | 1 | a0002c0003t0057 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3733G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3733 | chr12 | 68852704 | |||||
chr12:68852718
|
C | T | 2 | a0001c0001t0010a0001c0002t0010 | 6 | NA18949.hp1 NA18960.hp1 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3719G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3719 | chr12 | 68852718 | |||||
chr12:68852719
|
G | A | 2 | a0002c0005t0021a0002c0005t0023 | 4 | HG02486.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3718C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3718 | chr12 | 68852719 | |||||
chr12:68852725
|
T | A | 1 | a0001c0006t0040 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3712A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3712 | chr12 | 68852725 | |||||
chr12:68852824
|
A | T | 2 | a0002c0005t0021a0002c0005t0023 | 4 | HG02486.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3613T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3613 | chr12 | 68852824 | |||||
chr12:68852877
|
C | T | 94 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(91): Show | 312 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(309): Show |
3_prime_UTR_variant | MODIFIER | c.*3560G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3560 | chr12 | 68852877 | |||||
chr12:68853189
|
G | A | 2 | a0001c0002t0048a0002c0003t0027 | 2 | HG01109.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3248C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3248 | chr12 | 68853189 | |||||
chr12:68853204
|
G | GCTAT | 1 | a0002c0003t0015 | 3 | HG02717.hp2 HG03225.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3229_*3232dupATAG | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3232 | chr12 | 68853204 | |||||
chr12:68853275
|
C | T | 1 | a0001c0001t0067 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3162G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 3162 | chr12 | 68853275 | |||||
chr12:68853448
|
TAATTGGT others(14): Show |
T | 1 | a0002c0005t0021 | 2 | HG02723.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2968_*2988delGGAG others(17): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2968 | chr12 | 68853448 | |||||
chr12:68853449
|
A | C | 2 | a0001c0001t0024a0001c0004t0038 | 3 | HG00099.hp1 HG00733.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2988T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2988 | chr12 | 68853449 | |||||
chr12:68853470
|
A | G | 1 | a0001c0001t0056 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2967T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2967 | chr12 | 68853470 | |||||
chr12:68853479
|
A | G | 1 | a0001c0001t0055 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2958T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2958 | chr12 | 68853479 | |||||
chr12:68853569
|
G | A | 1 | a0002c0009t0044 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2868C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2868 | chr12 | 68853569 | |||||
chr12:68853667
|
C | T | 4 | a0002c0005t0021a0002c0005t0023a0002c0008t0034others(1): Show | 6 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2770G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2770 | chr12 | 68853667 | |||||
chr12:68853703
|
C | T | 17 | a0001c0001t0026a0001c0001t0067a0001c0002t0068others(14): Show | 28 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2734G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2734 | chr12 | 68853703 | |||||
chr12:68853710
|
T | G | 1 | a0001c0007t0045 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2727A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2727 | chr12 | 68853710 | |||||
chr12:68853763
|
C | T | 1 | a0001c0002t0054 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2674G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2674 | chr12 | 68853763 | |||||
chr12:68853764
|
G | A | 1 | a0001c0002t0062 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2673C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2673 | chr12 | 68853764 | |||||
chr12:68853777
|
A | G | 3 | a0002c0003t0032a0002c0003t0033a0002c0005t0016 | 4 | HG02895.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2660T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2660 | chr12 | 68853777 | |||||
chr12:68853889
|
G | T | 2 | a0001c0004t0011a0001c0016t0011 | 5 | HG01071.hp2 HG01081.hp2 HG01891.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2548C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2548 | chr12 | 68853889 | |||||
chr12:68853890
|
C | T | 2 | a0001c0004t0011a0001c0016t0011 | 5 | HG01071.hp2 HG01081.hp2 HG01891.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2547G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2547 | chr12 | 68853890 | |||||
chr12:68853892
|
A | T | 2 | a0001c0004t0011a0001c0016t0011 | 5 | HG01071.hp2 HG01081.hp2 HG01891.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2545T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2545 | chr12 | 68853892 | |||||
chr12:68853917
|
G | T | 10 | a0001c0001t0004a0001c0001t0066a0001c0002t0004others(7): Show | 18 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2520C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2520 | chr12 | 68853917 | |||||
chr12:68854168
|
C | T | 9 | a0001c0004t0005a0001c0004t0011a0001c0004t0036others(6): Show | 20 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2269G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2269 | chr12 | 68854168 | |||||
chr12:68854268
|
C | T | 10 | a0001c0002t0007a0001c0004t0008a0001c0004t0012others(7): Show | 19 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2169G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 2169 | chr12 | 68854268 | |||||
chr12:68854512
|
G | A | 1 | a0002c0005t0023 | 2 | HG02486.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1925C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1925 | chr12 | 68854512 | |||||
chr12:68854552
|
T | C | 4 | a0001c0001t0026a0001c0001t0067a0001c0002t0068others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1885A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1885 | chr12 | 68854552 | |||||
chr12:68854926
|
G | A | 9 | a0001c0002t0031a0001c0004t0017a0001c0004t0020others(6): Show | 12 | HG01361.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1511C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1511 | chr12 | 68854926 | |||||
chr12:68854950
|
AGGTTCAA others(875): Show |
A | 1 | a0001c0006t0047 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605_*1486del | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 605 | chr12 | 68854950 | |||||
chr12:68855017
|
C | T | 21 | a0001c0002t0031a0001c0004t0005a0001c0004t0011others(18): Show | 36 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1420G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1420 | chr12 | 68855017 | |||||
chr12:68855023
|
A | AT | 24 | a0001c0001t0051a0001c0001t0052a0001c0001t0053others(21): Show | 39 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1413dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1413 | chr12 | 68855023 | |||||
chr12:68855296
|
G | C | 1 | a0001c0006t0039 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1141C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1141 | chr12 | 68855296 | |||||
chr12:68855307
|
A | G | 21 | a0001c0002t0031a0001c0004t0005a0001c0004t0011others(18): Show | 36 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1130T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1130 | chr12 | 68855307 | |||||
chr12:68855396
|
G | A | 1 | a0001c0002t0063 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1041C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 1041 | chr12 | 68855396 | |||||
chr12:68855649
|
T | C | 1 | a0002c0010t0046 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 788 | chr12 | 68855649 | |||||
chr12:68855743
|
G | GT | 26 | a0001c0001t0004a0001c0001t0026a0001c0001t0066others(23): Show | 41 | HG01167.hp1 HG01891.hp2 HG02055.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*693dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 693 | chr12 | 68855743 | |||||
chr12:68855743
|
G | T | 4 | a0001c0004t0017a0001c0004t0020a0002c0005t0020others(1): Show | 6 | HG01361.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*694C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 694 | chr12 | 68855743 | |||||
chr12:68855800
|
A | T | 2 | a0002c0003t0019a0002c0008t0019 | 2 | HG02723.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*637T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 637 | chr12 | 68855800 | |||||
chr12:68855901
|
G | A | 2 | a0001c0002t0048a0002c0005t0023 | 3 | HG01109.hp2 HG02486.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*536C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 536 | chr12 | 68855901 | |||||
chr12:68855937
|
G | A | 1 | a0002c0005t0023 | 2 | HG02486.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*500C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 500 | chr12 | 68855937 | |||||
chr12:68855959
|
A | G | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*478T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 478 | chr12 | 68855959 | |||||
chr12:68855966
|
G | A | 29 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(26): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*471C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 471 | chr12 | 68855966 | |||||
chr12:68855989
|
C | T | 3 | a0001c0001t0018a0002c0003t0029a0002c0003t0030 | 4 | HG00639.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*448G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 448 | chr12 | 68855989 | |||||
chr12:68855998
|
C | A | 1 | a0001c0002t0064 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 439 | chr12 | 68855998 | |||||
chr12:68856091
|
C | T | 1 | a0001c0004t0017 | 2 | HG01361.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*346G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 346 | chr12 | 68856091 | |||||
chr12:68856147
|
C | T | 1 | a0002c0005t0016 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 290 | chr12 | 68856147 | |||||
chr12:68856229
|
T | C | 18 | a0001c0001t0004a0001c0001t0026a0001c0001t0066others(15): Show | 30 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*208A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 9/9 | 208 | chr12 | 68856229 | |||||
chr12:68933167
|
C | T | 2 | a0002c0003t0027a0002c0005t0016 | 3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 1/9 | 330 | chr12 | 68933167 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:68856701
|
T | C | 37 | a0001c0001t0002g0303a0001c0004t0002g0038a0001c0004t0005g0061others(34): Show | 38 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1090-22A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68856701 | ||||||
chr12:68856768
|
C | T | 197 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(194): Show | 198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1090-89G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68856768 | ||||||
chr12:68856854
|
G | A | 1 | a0001c0001t0067g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1090-175C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68856854 | ||||||
chr12:68856974
|
C | A | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1090-295G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68856974 | ||||||
chr12:68856983
|
C | T | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1090-304G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68856983 | ||||||
chr12:68857165
|
C | CT | 9 | a0001c0001t0001g0206a0001c0001t0002g0164a0001c0001t0002g0251others(6): Show | 9 | HG00558.hp1 HG01361.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1090-487dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857165 | ||||||
chr12:68857165
|
CT | C | 35 | a0001c0001t0001g0169a0001c0001t0001g0277a0001c0001t0024g0220others(32): Show | 36 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1090-487delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857165 | ||||||
chr12:68857364
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1090-685T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857364 | ||||||
chr12:68857429
|
G | A | 9 | a0001c0001t0002g0164a0001c0001t0002g0251a0001c0002t0002g0086others(6): Show | 9 | HG01516.hp2 HG01517.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1090-750C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857429 | ||||||
chr12:68857461
|
C | A | 1 | a0001c0007t0002g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1090-782G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857461 | ||||||
chr12:68857587
|
C | T | 35 | a0001c0004t0002g0038a0001c0004t0005g0061a0001c0004t0005g0145others(32): Show | 36 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1090-908G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857587 | ||||||
chr12:68857618
|
A | G | 3 | a0001c0002t0001g0084a0001c0002t0001g0270a0001c0002t0064g0101 | 3 | HG02083.hp1 NA18994.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1090-939T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857618 | ||||||
chr12:68857620
|
G | A | 11 | a0001c0001t0004g0112a0001c0001t0004g0229a0001c0001t0004g0298others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1090-941C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857620 | ||||||
chr12:68857641
|
G | A | 1 | a0001c0002t0001g0184 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1090-962C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857641 | ||||||
chr12:68857968
|
C | T | 17 | a0001c0001t0001g0130a0001c0001t0001g0219a0001c0001t0002g0303others(14): Show | 17 | HG00735.hp1 HG01123.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1089+955G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68857968 | ||||||
chr12:68858150
|
A | G | 30 | a0001c0001t0004g0112a0001c0001t0004g0203a0001c0001t0004g0229others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1089+773T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858150 | ||||||
chr12:68858212
|
C | A | 1 | a0002c0003t0027g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1089+711G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858212 | ||||||
chr12:68858271
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1089+652T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858271 | ||||||
chr12:68858367
|
G | A | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1089+556C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858367 | ||||||
chr12:68858375
|
T | C | 82 | a0001c0001t0001g0130a0001c0001t0001g0167a0001c0001t0001g0177others(79): Show | 82 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1089+548A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858375 | ||||||
chr12:68858450
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0304 | 2 | HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1089+473T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858450 | ||||||
chr12:68858731
|
TG | T | 53 | a0001c0004t0002g0038a0001c0004t0005g0061a0001c0004t0005g0148others(50): Show | 54 | HG00741.hp1 HG01071.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.1089+191delC | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858731 | ||||||
chr12:68858733
|
G | GT | 36 | a0001c0001t0002g0164a0001c0001t0002g0251a0001c0001t0004g0112others(33): Show | 36 | HG00438.hp2 HG01516.hp2 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.1089+189dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858733 | ||||||
chr12:68858733
|
G | T | 1 | a0001c0004t0005g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1089+190C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858733 | ||||||
chr12:68858735
|
T | G | 1 | a0002c0003t0057g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1089+188A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858735 | ||||||
chr12:68858814
|
G | A | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1089+109C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858814 | ||||||
chr12:68858814
|
G | C | 57 | a0001c0004t0002g0038a0001c0004t0005g0061a0001c0004t0005g0145others(54): Show | 58 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1089+109C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858814 | ||||||
chr12:68858849
|
G | A | 1 | a0001c0004t0011g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1089+74C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858849 | ||||||
chr12:68858869
|
A | G | 6 | a0001c0004t0017g0102a0001c0004t0017g0103a0001c0004t0020g0069others(3): Show | 6 | HG01361.hp2 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1089+54T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 8/8 | chr12 | 68858869 | ||||||
chr12:68859104
|
C | A | 1 | a0001c0001t0001g0213 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.941-33G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859104 | ||||||
chr12:68859281
|
C | T | 2 | a0001c0001t0001g0297a0001c0004t0011g0218 | 2 | HG01891.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.941-210G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859281 | ||||||
chr12:68859316
|
A | G | 1 | a0001c0002t0001g0043 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.941-245T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859316 | ||||||
chr12:68859451
|
A | G | 221 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(218): Show | 222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.941-380T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859451 | ||||||
chr12:68859603
|
T | C | 2 | a0001c0002t0048g0287a0002c0003t0027g0005 | 2 | HG01109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.941-532A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859603 | ||||||
chr12:68859761
|
G | A | 1 | a0001c0004t0036g0253 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.941-690C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859761 | ||||||
chr12:68859873
|
C | T | 3 | a0002c0003t0019g0026a0002c0005t0005g0014a0002c0008t0019g0325 | 3 | HG02723.hp2 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.941-802G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859873 | ||||||
chr12:68859888
|
T | C | 1 | a0001c0006t0047g0211 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.941-817A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859888 | ||||||
chr12:68859991
|
C | T | 2 | a0002c0003t0029g0018a0002c0003t0030g0030 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.941-920G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68859991 | ||||||
chr12:68860050
|
C | T | 1 | a0001c0001t0053g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.941-979G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860050 | ||||||
chr12:68860067
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.941-996C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860067 | ||||||
chr12:68860172
|
T | C | 1 | a0007c0017t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.941-1101A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860172 | ||||||
chr12:68860242
|
C | G | 1 | a0002c0008t0019g0325 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.941-1171G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860242 | ||||||
chr12:68860256
|
C | G | 2 | a0002c0005t0023g0011a0002c0005t0023g0012 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.941-1185G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860256 | ||||||
chr12:68860281
|
G | C | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.941-1210C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860281 | ||||||
chr12:68860375
|
C | G | 9 | a0001c0004t0008g0233a0001c0006t0008g0226a0001c0006t0008g0244others(6): Show | 9 | HG01167.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.941-1304G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860375 | ||||||
chr12:68860483
|
T | C | 59 | a0001c0001t0002g0303a0001c0004t0002g0038a0001c0004t0005g0061others(56): Show | 60 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.941-1412A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860483 | ||||||
chr12:68860542
|
GC | G | 13 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0039others(10): Show | 13 | HG00438.hp1 HG01099.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.941-1472delG | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860542 | ||||||
chr12:68860618
|
T | A | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.941-1547A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860618 | ||||||
chr12:68860966
|
G | A | 1 | a0001c0001t0058g0214 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.941-1895C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68860966 | ||||||
chr12:68861175
|
C | A | 28 | a0001c0001t0002g0303a0001c0004t0002g0038a0001c0004t0005g0061others(25): Show | 29 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.941-2104G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861175 | ||||||
chr12:68861432
|
T | A | 1 | a0002c0005t0022g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.941-2361A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861432 | ||||||
chr12:68861525
|
A | G | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.941-2454T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861525 | ||||||
chr12:68861540
|
G | GT | 62 | a0001c0001t0002g0164a0001c0001t0002g0251a0001c0001t0002g0303others(59): Show | 63 | HG00642.hp2 HG00733.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.941-2470dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861540 | ||||||
chr12:68861540
|
G | T | 2 | a0002c0003t0029g0018a0002c0003t0030g0030 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.941-2469C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861540 | ||||||
chr12:68861606
|
T | C | 304 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(301): Show | 306 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.941-2535A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861606 | ||||||
chr12:68861610
|
A | G | 57 | a0001c0001t0002g0303a0001c0004t0002g0038a0001c0004t0005g0061others(54): Show | 58 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.941-2539T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861610 | ||||||
chr12:68861613
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.941-2542A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861613 | ||||||
chr12:68861622
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.941-2551G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861622 | ||||||
chr12:68861659
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.941-2588C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861659 | ||||||
chr12:68861675
|
C | T | 302 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(299): Show | 304 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.941-2604G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861675 | ||||||
chr12:68861823
|
C | T | 2 | a0001c0001t0001g0263a0007c0017t0001g0055 | 2 | HG01071.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.941-2752G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861823 | ||||||
chr12:68861842
|
C | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0267a0001c0001t0014g0118others(1): Show | 4 | HG02080.hp2 NA18612.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-2771G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861842 | ||||||
chr12:68861856
|
A | G | 2 | a0002c0005t0021g0331a0002c0005t0021g0333 | 2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.941-2785T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861856 | ||||||
chr12:68861910
|
C | CA | 10 | a0001c0001t0018g0232a0001c0002t0002g0049a0001c0007t0009g0076others(7): Show | 10 | HG01358.hp2 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.941-2840dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861910 | ||||||
chr12:68861910
|
CA | C | 218 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0072others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.941-2840delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861910 | ||||||
chr12:68861910
|
CAA | C | 30 | a0001c0001t0001g0070a0001c0001t0001g0176a0001c0001t0001g0267others(27): Show | 30 | HG01516.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.941-2841_941-2840d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861910 | ||||||
chr12:68861910
|
CAAA | C | 8 | a0001c0001t0004g0203a0001c0002t0065g0111a0002c0003t0004g0019others(5): Show | 8 | HG02559.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-2842_941-2840d others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861910 | ||||||
chr12:68861932
|
A | G | 1 | a0001c0001t0056g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.941-2861T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861932 | ||||||
chr12:68861946
|
C | G | 8 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0151others(5): Show | 8 | HG02074.hp1 HG02165.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-2875G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861946 | ||||||
chr12:68861949
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.941-2878A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861949 | ||||||
chr12:68861995
|
TTTAATAG others(735): Show |
T | 57 | a0001c0001t0002g0303a0001c0004t0002g0038a0001c0004t0005g0061others(54): Show | 58 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.941-3666_941-2925d others(2): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68861995 | ||||||
chr12:68862074
|
C | T | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.941-3003G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862074 | ||||||
chr12:68862119
|
C | T | 3 | a0001c0001t0001g0060a0001c0002t0001g0191a0001c0002t0001g0258 | 3 | HG00642.hp1 HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.941-3048G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862119 | ||||||
chr12:68862173
|
A | G | 215 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(212): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.941-3102T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862173 | ||||||
chr12:68862328
|
G | A | 28 | a0001c0001t0004g0112a0001c0001t0004g0203a0001c0001t0004g0229others(25): Show | 28 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.941-3257C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862328 | ||||||
chr12:68862559
|
T | G | 10 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0188others(7): Show | 10 | HG00099.hp1 HG00735.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.941-3488A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862559 | ||||||
chr12:68862913
|
T | C | 9 | a0001c0001t0026g0231a0001c0002t0007g0095a0001c0002t0007g0247others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.941-3842A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862913 | ||||||
chr12:68862945
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.941-3874C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68862945 | ||||||
chr12:68863085
|
T | G | 28 | a0001c0001t0004g0112a0001c0001t0004g0203a0001c0001t0004g0229others(25): Show | 28 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.940+3811A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863085 | ||||||
chr12:68863450
|
A | G | 5 | a0001c0001t0002g0164a0001c0001t0002g0251a0001c0002t0002g0086others(2): Show | 5 | HG01516.hp2 HG01517.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.940+3446T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863450 | ||||||
chr12:68863514
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.940+3382A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863514 | ||||||
chr12:68863613
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.940+3283C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863613 | ||||||
chr12:68863645
|
C | T | 4 | a0001c0004t0017g0102a0001c0004t0017g0103a0001c0004t0020g0069others(1): Show | 4 | HG01361.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+3251G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863645 | ||||||
chr12:68863662
|
C | A | 201 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(198): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.940+3234G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863662 | ||||||
chr12:68863662
|
C | T | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.940+3234G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863662 | ||||||
chr12:68863717
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.940+3179G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863717 | ||||||
chr12:68863726
|
T | C | 13 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0039others(10): Show | 13 | HG00438.hp1 HG01099.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+3170A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863726 | ||||||
chr12:68863962
|
G | C | 20 | a0001c0001t0004g0112a0001c0001t0004g0229a0001c0001t0004g0298others(17): Show | 20 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.940+2934C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68863962 | ||||||
chr12:68864216
|
C | T | 1 | a0002c0003t0004g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.940+2680G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864216 | ||||||
chr12:68864271
|
C | G | 2 | a0002c0003t0019g0026a0002c0008t0019g0325 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.940+2625G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864271 | ||||||
chr12:68864309
|
G | A | 197 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(194): Show | 198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.940+2587C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864309 | ||||||
chr12:68864439
|
C | T | 8 | a0001c0001t0004g0203a0001c0002t0065g0111a0002c0003t0004g0019others(5): Show | 8 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.940+2457G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864439 | ||||||
chr12:68864664
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156 | 3 | NA18943.hp2 NA18951.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.940+2232C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864664 | ||||||
chr12:68864675
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.940+2221G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864675 | ||||||
chr12:68864700
|
G | T | 1 | a0001c0002t0050g0092 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.940+2196C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68864700 | ||||||
chr12:68865005
|
A | T | 4 | a0001c0004t0017g0102a0001c0004t0017g0103a0001c0004t0020g0069others(1): Show | 4 | HG01361.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.940+1891T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865005 | ||||||
chr12:68865007
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.940+1889G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865007 | ||||||
chr12:68865044
|
T | C | 4 | a0002c0003t0019g0026a0002c0005t0021g0331a0002c0005t0021g0333others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+1852A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865044 | ||||||
chr12:68865048
|
T | A | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.940+1848A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865048 | ||||||
chr12:68865376
|
C | G | 336 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.940+1520G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865376 | ||||||
chr12:68865437
|
C | T | 54 | a0001c0001t0001g0189a0001c0001t0001g0207a0001c0001t0002g0303others(51): Show | 56 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.940+1459G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865437 | ||||||
chr12:68865558
|
G | A | 47 | a0001c0001t0002g0303a0001c0001t0004g0298a0001c0004t0002g0038others(44): Show | 48 | HG00733.hp2 HG00741.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.940+1338C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865558 | ||||||
chr12:68865634
|
T | A | 48 | a0001c0001t0002g0303a0001c0001t0004g0298a0001c0004t0002g0038others(45): Show | 49 | HG00733.hp2 HG00741.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.940+1262A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865634 | ||||||
chr12:68865636
|
A | T | 48 | a0001c0001t0002g0303a0001c0001t0004g0298a0001c0004t0002g0038others(45): Show | 49 | HG00733.hp2 HG00741.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.940+1260T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865636 | ||||||
chr12:68865638
|
ACTCT | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0288a0001c0002t0001g0283 | 3 | HG02129.hp2 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.940+1254_940+1257d others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865638 | ||||||
chr12:68865640
|
T | A | 48 | a0001c0001t0002g0303a0001c0001t0004g0298a0001c0004t0002g0038others(45): Show | 49 | HG00733.hp2 HG00741.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.940+1256A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865640 | ||||||
chr12:68865710
|
C | G | 106 | a0001c0001t0001g0130a0001c0001t0001g0213a0001c0001t0001g0219others(103): Show | 107 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.940+1186G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865710 | ||||||
chr12:68865968
|
G | A | 5 | a0001c0001t0002g0164a0001c0001t0002g0251a0001c0002t0002g0266others(2): Show | 5 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+928C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68865968 | ||||||
chr12:68866096
|
G | A | 1 | a0001c0006t0008g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.940+800C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866096 | ||||||
chr12:68866105
|
AG | A | 4 | a0001c0001t0002g0164a0001c0001t0002g0251a0001c0002t0002g0264others(1): Show | 4 | HG01516.hp2 HG01517.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+790delC | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866105 | ||||||
chr12:68866249
|
A | G | 2 | a0001c0002t0004g0246a0002c0005t0022g0326 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.940+647T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866249 | ||||||
chr12:68866324
|
A | ATGTT | 6 | a0001c0001t0004g0112a0002c0003t0004g0314a0002c0003t0030g0030others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+568_940+571dup others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866324 | ||||||
chr12:68866324
|
ATGTT | A | 6 | a0001c0002t0001g0144a0001c0002t0009g0057a0001c0004t0011g0056others(3): Show | 6 | HG00408.hp1 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+568_940+571del others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866324 | ||||||
chr12:68866330
|
G | T | 1 | a0002c0009t0001g0311 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.940+566C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866330 | ||||||
chr12:68866401
|
T | G | 1 | a0002c0010t0002g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.940+495A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866401 | ||||||
chr12:68866563
|
C | T | 1 | a0001c0001t0067g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.940+333G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866563 | ||||||
chr12:68866588
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.940+308G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866588 | ||||||
chr12:68866691
|
C | T | 1 | a0002c0005t0022g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.940+205G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866691 | ||||||
chr12:68866820
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.940+76G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 7/8 | chr12 | 68866820 | ||||||
chr12:68867074
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.788-26C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867074 | ||||||
chr12:68867079
|
G | C | 2 | a0001c0007t0001g0132a0001c0016t0011g0127 | 2 | HG01081.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.788-31C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867079 | ||||||
chr12:68867104
|
T | A | 1 | a0002c0005t0002g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.788-56A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867104 | ||||||
chr12:68867163
|
T | C | 3 | a0002c0003t0015g0332a0002c0005t0021g0331a0002c0005t0021g0333 | 3 | HG02723.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.788-115A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867163 | ||||||
chr12:68867264
|
C | T | 235 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(232): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.788-216G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867264 | ||||||
chr12:68867300
|
T | A | 3 | a0001c0002t0002g0086a0001c0002t0002g0264a0001c0002t0002g0266 | 3 | HG01993.hp1 HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.788-252A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867300 | ||||||
chr12:68867620
|
C | T | 2 | a0002c0003t0032g0335a0002c0003t0033g0336 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.788-572G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867620 | ||||||
chr12:68867677
|
C | T | 152 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(149): Show | 153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.788-629G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867677 | ||||||
chr12:68867690
|
C | T | 4 | a0001c0002t0010g0093a0001c0002t0010g0187a0001c0002t0010g0292others(1): Show | 4 | NA18960.hp1 NA18971.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-642G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867690 | ||||||
chr12:68867754
|
G | A | 2 | a0002c0003t0004g0019a0002c0010t0002g0022 | 2 | HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.788-706C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867754 | ||||||
chr12:68867758
|
C | T | 1 | a0002c0005t0002g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.788-710G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867758 | ||||||
chr12:68867759
|
G | A | 7 | a0002c0003t0003g0015a0002c0005t0016g0003a0002c0005t0016g0004others(4): Show | 7 | HG02145.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.788-711C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867759 | ||||||
chr12:68867781
|
G | A | 1 | a0001c0002t0063g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.788-733C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867781 | ||||||
chr12:68867979
|
T | G | 71 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0053g0243others(68): Show | 71 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.788-931A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867979 | ||||||
chr12:68867988
|
C | T | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.788-940G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68867988 | ||||||
chr12:68868042
|
A | T | 2 | a0002c0003t0029g0018a0002c0005t0022g0326 | 2 | HG00639.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.788-994T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868042 | ||||||
chr12:68868141
|
A | G | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.788-1093T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868141 | ||||||
chr12:68868143
|
G | A | 1 | a0005c0014t0001g0337 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.788-1095C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868143 | ||||||
chr12:68868217
|
C | T | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.787+1108G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868217 | ||||||
chr12:68868357
|
C | T | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.787+968G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868357 | ||||||
chr12:68868436
|
G | A | 1 | a0001c0006t0005g0296 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.787+889C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868436 | ||||||
chr12:68868533
|
G | A | 2 | a0002c0003t0032g0335a0002c0003t0033g0336 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.787+792C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868533 | ||||||
chr12:68868574
|
G | A | 1 | a0001c0002t0007g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.787+751C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868574 | ||||||
chr12:68868738
|
G | A | 1 | a0001c0004t0008g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.787+587C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868738 | ||||||
chr12:68868938
|
C | A | 9 | a0002c0003t0003g0016a0002c0003t0004g0019a0002c0003t0027g0005others(6): Show | 9 | HG02258.hp2 HG02486.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.787+387G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68868938 | ||||||
chr12:68869189
|
G | C | 4 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0264others(1): Show | 4 | HG01993.hp1 HG02698.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.787+136C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 6/8 | chr12 | 68869189 | ||||||
chr12:68869696
|
T | C | 3 | a0001c0006t0012g0225a0001c0006t0012g0241a0001c0006t0040g0242 | 3 | HG02572.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.617-201A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 5/8 | chr12 | 68869696 | ||||||
chr12:68869817
|
T | A | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.617-322A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 5/8 | chr12 | 68869817 | ||||||
chr12:68869880
|
CA | C | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.616+334delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 5/8 | chr12 | 68869880 | ||||||
chr12:68869888
|
A | C | 1 | a0001c0002t0001g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.616+327T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 5/8 | chr12 | 68869888 | ||||||
chr12:68869891
|
G | GT | 142 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.616+323dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 5/8 | chr12 | 68869891 | ||||||
chr12:68870199
|
A | G | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.616+16T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 5/8 | chr12 | 68870199 | ||||||
chr12:68870438
|
C | T | 1 | a0001c0002t0001g0270 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.432-39G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870438 | ||||||
chr12:68870709
|
G | A | 2 | a0001c0004t0020g0069a0002c0005t0020g0316 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.432-310C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870709 | ||||||
chr12:68870726
|
C | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.432-327G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870726 | ||||||
chr12:68870744
|
A | G | 6 | a0001c0002t0001g0117a0001c0002t0001g0131a0001c0002t0001g0138others(3): Show | 6 | HG00438.hp2 HG02056.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-345T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870744 | ||||||
chr12:68870752
|
TGTCTCAG others(5): Show |
T | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.432-365_432-354del others(12): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870752 | ||||||
chr12:68870778
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0109a0001c0001t0001g0160others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.432-379G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870778 | ||||||
chr12:68870795
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.432-396T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870795 | ||||||
chr12:68870964
|
C | G | 2 | a0001c0004t0011g0058a0001c0004t0011g0209 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.432-565G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68870964 | ||||||
chr12:68871023
|
T | C | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.432-624A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871023 | ||||||
chr12:68871334
|
A | T | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.431+450T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871334 | ||||||
chr12:68871416
|
C | T | 139 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(136): Show | 140 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.431+368G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871416 | ||||||
chr12:68871465
|
G | A | 4 | a0001c0001t0001g0263a0001c0001t0003g0265a0001c0001t0024g0220others(1): Show | 4 | HG00099.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.431+319C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871465 | ||||||
chr12:68871498
|
C | G | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.431+286G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871498 | ||||||
chr12:68871531
|
G | A | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431+253C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871531 | ||||||
chr12:68871657
|
A | G | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.431+127T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871657 | ||||||
chr12:68871672
|
G | T | 1 | a0001c0002t0003g0272 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.431+112C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 4/8 | chr12 | 68871672 | ||||||
chr12:68872021
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0155a0001c0001t0010g0236 | 3 | NA18961.hp1 NA19003.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.259-65G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872021 | ||||||
chr12:68872080
|
T | C | 2 | a0002c0008t0004g0020a0002c0010t0046g0029 | 2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.259-124A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872080 | ||||||
chr12:68872230
|
A | ATGC | 5 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0086others(2): Show | 5 | HG01993.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-277_259-275dup others(3): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872230 | ||||||
chr12:68872230
|
A | ATGCTGC | 76 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(73): Show | 76 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.259-280_259-275dup others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872230 | ||||||
chr12:68872247
|
G | C | 1 | a0001c0002t0050g0092 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.259-291C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872247 | ||||||
chr12:68872251
|
C | T | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-295G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872251 | ||||||
chr12:68872252
|
C | CT | 143 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(140): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.259-297dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872252 | ||||||
chr12:68872252
|
C | CTT | 45 | a0001c0002t0001g0043a0001c0002t0001g0117a0001c0002t0001g0125others(42): Show | 45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.259-298_259-297dup others(2): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872252 | ||||||
chr12:68872253
|
T | C | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-297A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872253 | ||||||
chr12:68872279
|
T | C | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-323A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872279 | ||||||
chr12:68872309
|
T | G | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-353A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872309 | ||||||
chr12:68872315
|
C | T | 3 | a0001c0002t0007g0095a0002c0003t0004g0023a0002c0003t0028g0006 | 3 | HG02559.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.259-359G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872315 | ||||||
chr12:68872332
|
A | C | 1 | a0002c0010t0008g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.259-376T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872332 | ||||||
chr12:68872398
|
G | A | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-442C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872398 | ||||||
chr12:68872400
|
G | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-444C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872400 | ||||||
chr12:68872410
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.259-454C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872410 | ||||||
chr12:68872412
|
C | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-456G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872412 | ||||||
chr12:68872441
|
T | C | 135 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(132): Show | 135 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.259-485A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872441 | ||||||
chr12:68872442
|
G | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-486C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872442 | ||||||
chr12:68872515
|
A | G | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-559T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872515 | ||||||
chr12:68872544
|
C | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-588G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872544 | ||||||
chr12:68872555
|
A | C | 1 | a0001c0001t0014g0291 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.259-599T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872555 | ||||||
chr12:68872627
|
T | C | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-671A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872627 | ||||||
chr12:68872725
|
C | A | 1 | a0002c0005t0002g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.259-769G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872725 | ||||||
chr12:68872732
|
T | C | 3 | a0001c0006t0005g0296a0001c0006t0037g0224a0001c0006t0047g0211 | 3 | HG02738.hp1 HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.259-776A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872732 | ||||||
chr12:68872738
|
AT | A | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-783delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872738 | ||||||
chr12:68872739
|
T | C | 34 | a0001c0002t0001g0117a0001c0002t0001g0125a0001c0002t0001g0131others(31): Show | 34 | HG00099.hp2 HG00438.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.259-783A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872739 | ||||||
chr12:68872855
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-899T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872855 | ||||||
chr12:68872856
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-900T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872856 | ||||||
chr12:68872857
|
G | C | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-901C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872857 | ||||||
chr12:68872858
|
C | A | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-902G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872858 | ||||||
chr12:68872948
|
A | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-992T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872948 | ||||||
chr12:68872980
|
G | T | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-1024C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68872980 | ||||||
chr12:68873104
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-1148T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873104 | ||||||
chr12:68873105
|
T | C | 13 | a0001c0002t0007g0095a0001c0002t0065g0111a0001c0004t0008g0233others(10): Show | 13 | HG00639.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.259-1149A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873105 | ||||||
chr12:68873147
|
T | G | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-1191A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873147 | ||||||
chr12:68873233
|
C | T | 4 | a0003c0011t0012g0028a0003c0012t0007g0334a0004c0013t0004g0027others(1): Show | 4 | HG03130.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-1277G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873233 | ||||||
chr12:68873240
|
T | A | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-1284A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873240 | ||||||
chr12:68873326
|
A | G | 61 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(58): Show | 61 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.259-1370T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873326 | ||||||
chr12:68873330
|
C | T | 61 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(58): Show | 61 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.259-1374G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873330 | ||||||
chr12:68873372
|
G | A | 1 | a0002c0005t0022g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.259-1416C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873372 | ||||||
chr12:68873468
|
C | T | 140 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.259-1512G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873468 | ||||||
chr12:68873590
|
C | T | 3 | a0002c0008t0004g0020a0002c0010t0002g0022a0002c0010t0046g0029 | 3 | HG02280.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.259-1634G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873590 | ||||||
chr12:68873667
|
C | CA | 8 | a0001c0001t0001g0161a0001c0001t0001g0297a0001c0001t0026g0231others(5): Show | 8 | HG00741.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-1712dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873667 | ||||||
chr12:68873667
|
CA | C | 81 | a0001c0001t0001g0166a0001c0001t0001g0238a0001c0001t0001g0290others(78): Show | 81 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.259-1712delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873667 | ||||||
chr12:68873806
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.259-1850A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873806 | ||||||
chr12:68873926
|
C | A | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259-1970G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873926 | ||||||
chr12:68873943
|
T | C | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-1987A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68873943 | ||||||
chr12:68874025
|
C | T | 16 | a0001c0002t0004g0246a0001c0002t0031g0050a0001c0004t0020g0069others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-2069G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874025 | ||||||
chr12:68874073
|
C | G | 1 | a0001c0001t0001g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.259-2117G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874073 | ||||||
chr12:68874073
|
C | T | 216 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.259-2117G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874073 | ||||||
chr12:68874096
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156 | 3 | NA18943.hp2 NA18951.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.259-2140G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874096 | ||||||
chr12:68874150
|
A | G | 16 | a0001c0002t0004g0246a0001c0002t0031g0050a0001c0004t0020g0069others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-2194T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874150 | ||||||
chr12:68874163
|
C | G | 16 | a0001c0002t0004g0246a0001c0002t0031g0050a0001c0004t0020g0069others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-2207G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874163 | ||||||
chr12:68874233
|
C | G | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.259-2277G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874233 | ||||||
chr12:68874390
|
T | C | 80 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(77): Show | 80 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.259-2434A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874390 | ||||||
chr12:68874531
|
G | A | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-2575C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874531 | ||||||
chr12:68874581
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.259-2625G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874581 | ||||||
chr12:68874888
|
C | T | 1 | a0007c0017t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.259-2932G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68874888 | ||||||
chr12:68875017
|
T | G | 4 | a0003c0011t0012g0028a0003c0012t0007g0334a0004c0013t0004g0027others(1): Show | 4 | HG03130.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-3061A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875017 | ||||||
chr12:68875058
|
A | T | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.259-3102T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875058 | ||||||
chr12:68875099
|
C | T | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259-3143G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875099 | ||||||
chr12:68875100
|
A | C | 222 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(219): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.259-3144T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875100 | ||||||
chr12:68875148
|
G | C | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-3192C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875148 | ||||||
chr12:68875180
|
G | A | 1 | a0001c0002t0001g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.259-3224C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875180 | ||||||
chr12:68875182
|
C | T | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259-3226G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875182 | ||||||
chr12:68875249
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.259-3293C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875249 | ||||||
chr12:68875275
|
T | C | 80 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(77): Show | 80 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.259-3319A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875275 | ||||||
chr12:68875276
|
G | A | 2 | a0002c0005t0023g0011a0002c0005t0023g0012 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.259-3320C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875276 | ||||||
chr12:68875300
|
G | A | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-3344C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875300 | ||||||
chr12:68875330
|
A | G | 77 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(74): Show | 77 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.259-3374T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875330 | ||||||
chr12:68875345
|
A | G | 5 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0086others(2): Show | 5 | HG01993.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-3389T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875345 | ||||||
chr12:68875362
|
AAAG | A | 140 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.259-3409_259-3407d others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875362 | ||||||
chr12:68875449
|
T | C | 1 | a0001c0002t0006g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.259-3493A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875449 | ||||||
chr12:68875487
|
A | T | 16 | a0001c0002t0004g0246a0001c0002t0031g0050a0001c0004t0020g0069others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-3531T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875487 | ||||||
chr12:68875595
|
A | C | 274 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.259-3639T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875595 | ||||||
chr12:68875668
|
T | C | 1 | a0002c0003t0004g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.259-3712A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875668 | ||||||
chr12:68875775
|
T | C | 219 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(216): Show | 220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.259-3819A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875775 | ||||||
chr12:68875803
|
C | CA | 120 | a0001c0001t0067g0083a0001c0002t0001g0034a0001c0002t0001g0035others(117): Show | 120 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.259-3848dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68875803 | ||||||
chr12:68876152
|
A | G | 1 | a0001c0007t0001g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.259-4196T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876152 | ||||||
chr12:68876181
|
T | C | 4 | a0002c0003t0015g0330a0002c0003t0015g0332a0002c0005t0021g0331others(1): Show | 4 | HG02723.hp1 HG02818.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-4225A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876181 | ||||||
chr12:68876216
|
A | G | 5 | a0001c0001t0001g0140a0001c0001t0001g0177a0001c0001t0001g0183others(2): Show | 5 | NA18747.hp1 NA18975.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-4260T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876216 | ||||||
chr12:68876261
|
C | A | 64 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.259-4305G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876261 | ||||||
chr12:68876697
|
G | A | 274 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.259-4741C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876697 | ||||||
chr12:68876745
|
C | T | 3 | a0001c0001t0053g0243a0002c0008t0019g0325a0002c0008t0034g0327 | 3 | HG02055.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.259-4789G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876745 | ||||||
chr12:68876845
|
T | C | 277 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.259-4889A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876845 | ||||||
chr12:68876886
|
G | A | 14 | a0001c0002t0007g0095a0001c0002t0065g0111a0001c0004t0008g0233others(11): Show | 14 | HG00639.hp1 HG01361.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.259-4930C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876886 | ||||||
chr12:68876893
|
CGT | C | 65 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(62): Show | 65 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.259-4939_259-4938d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876893 | ||||||
chr12:68876893
|
CGTGT | C | 16 | a0001c0002t0004g0246a0001c0002t0031g0050a0001c0002t0065g0111others(13): Show | 16 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.259-4941_259-4938d others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876893 | ||||||
chr12:68876894
|
G | A | 8 | a0001c0004t0008g0233a0002c0003t0019g0026a0002c0003t0029g0018others(5): Show | 8 | HG00639.hp1 HG02145.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-4938C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876894 | ||||||
chr12:68876896
|
G | A | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259-4940C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876896 | ||||||
chr12:68876898
|
G | A | 1 | a0001c0002t0065g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.259-4942C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876898 | ||||||
chr12:68876907
|
T | C | 15 | a0001c0002t0004g0246a0001c0002t0031g0050a0001c0004t0020g0069others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.259-4951A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876907 | ||||||
chr12:68876915
|
T | A | 1 | a0001c0002t0001g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.259-4959A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876915 | ||||||
chr12:68876915
|
TGTGTGA | T | 134 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.259-4965_259-4960d others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876915 | ||||||
chr12:68876915
|
TGTGTGAG others(3): Show |
T | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259-4969_259-4960d others(12): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876915 | ||||||
chr12:68876917
|
T | A | 64 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(61): Show | 64 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.259-4961A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876917 | ||||||
chr12:68876919
|
T | A | 91 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(88): Show | 91 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.259-4963A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68876919 | ||||||
chr12:68877503
|
C | A | 89 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.259-5547G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877503 | ||||||
chr12:68877517
|
A | G | 1 | a0005c0014t0001g0337 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.259-5561T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877517 | ||||||
chr12:68877531
|
A | C | 272 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.259-5575T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877531 | ||||||
chr12:68877564
|
C | G | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259-5608G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877564 | ||||||
chr12:68877665
|
T | G | 89 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.259-5709A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877665 | ||||||
chr12:68877670
|
C | A | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-5714G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877670 | ||||||
chr12:68877706
|
GA | G | 89 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.259-5751delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877706 | ||||||
chr12:68877871
|
C | T | 89 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.259-5915G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877871 | ||||||
chr12:68877902
|
C | T | 14 | a0001c0002t0007g0095a0001c0002t0065g0111a0001c0004t0008g0233others(11): Show | 14 | HG00639.hp1 HG01361.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.259-5946G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877902 | ||||||
chr12:68877908
|
G | C | 1 | a0002c0003t0001g0313 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.259-5952C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877908 | ||||||
chr12:68877926
|
C | T | 1 | a0001c0002t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.259-5970G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68877926 | ||||||
chr12:68878106
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.259-6150C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878106 | ||||||
chr12:68878353
|
T | C | 1 | a0001c0004t0020g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259-6397A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878353 | ||||||
chr12:68878364
|
G | T | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.259-6408C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878364 | ||||||
chr12:68878385
|
C | G | 1 | a0001c0002t0006g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259-6429G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878385 | ||||||
chr12:68878388
|
A | G | 2 | a0002c0009t0002g0031a0002c0009t0002g0032 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.259-6432T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878388 | ||||||
chr12:68878565
|
G | A | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259-6609C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878565 | ||||||
chr12:68878759
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0251 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.259-6803C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878759 | ||||||
chr12:68878778
|
C | T | 3 | a0002c0008t0004g0020a0002c0010t0002g0022a0002c0010t0046g0029 | 3 | HG02280.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.259-6822G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878778 | ||||||
chr12:68878911
|
G | T | 5 | a0001c0001t0001g0234a0001c0001t0009g0235a0001c0006t0005g0296others(2): Show | 5 | HG00140.hp1 HG02738.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+6881C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878911 | ||||||
chr12:68878914
|
G | A | 2 | a0002c0005t0023g0011a0002c0005t0023g0012 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.258+6878C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878914 | ||||||
chr12:68878967
|
C | T | 11 | a0002c0003t0003g0016a0002c0003t0004g0019a0002c0003t0027g0005others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+6825G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68878967 | ||||||
chr12:68879257
|
C | A | 89 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(86): Show | 89 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.258+6535G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68879257 | ||||||
chr12:68879292
|
A | G | 1 | a0001c0002t0001g0090 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.258+6500T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68879292 | ||||||
chr12:68879455
|
C | G | 1 | a0001c0002t0001g0257 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.258+6337G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68879455 | ||||||
chr12:68879567
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.258+6225C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68879567 | ||||||
chr12:68879669
|
C | A | 2 | a0001c0002t0001g0278a0001c0002t0003g0146 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.258+6123G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68879669 | ||||||
chr12:68880105
|
T | TA | 269 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.258+5686dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880105 | ||||||
chr12:68880248
|
T | C | 1 | a0002c0005t0022g0318 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.258+5544A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880248 | ||||||
chr12:68880450
|
C | T | 269 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.258+5342G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880450 | ||||||
chr12:68880550
|
A | C | 1 | a0001c0002t0007g0095 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.258+5242T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880550 | ||||||
chr12:68880555
|
A | T | 1 | a0001c0002t0065g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.258+5237T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880555 | ||||||
chr12:68880663
|
C | T | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.258+5129G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880663 | ||||||
chr12:68880704
|
C | G | 78 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(75): Show | 78 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.258+5088G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880704 | ||||||
chr12:68880775
|
C | T | 67 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(64): Show | 67 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.258+5017G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880775 | ||||||
chr12:68880807
|
T | G | 14 | a0001c0002t0007g0095a0001c0002t0065g0111a0001c0004t0008g0233others(11): Show | 14 | HG00639.hp1 HG01361.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+4985A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880807 | ||||||
chr12:68880849
|
C | T | 31 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(28): Show | 31 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.258+4943G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880849 | ||||||
chr12:68880877
|
G | A | 1 | a0002c0005t0035g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.258+4915C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68880877 | ||||||
chr12:68881083
|
T | C | 8 | a0001c0002t0007g0095a0001c0002t0065g0111a0001c0004t0008g0233others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+4709A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881083 | ||||||
chr12:68881091
|
G | A | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.258+4701C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881091 | ||||||
chr12:68881219
|
G | T | 1 | a0003c0012t0007g0334 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.258+4573C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881219 | ||||||
chr12:68881418
|
C | T | 268 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.258+4374G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881418 | ||||||
chr12:68881577
|
A | AG | 269 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.258+4214_258+4215i others(3): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881577 | ||||||
chr12:68881673
|
T | C | 85 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(82): Show | 85 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.258+4119A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881673 | ||||||
chr12:68881674
|
G | A | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.258+4118C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881674 | ||||||
chr12:68881727
|
CT | C | 259 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.258+4064delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881727 | ||||||
chr12:68881760
|
G | A | 1 | a0001c0002t0001g0079 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.258+4032C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881760 | ||||||
chr12:68881843
|
A | C | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+3949T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881843 | ||||||
chr12:68881993
|
A | T | 1 | a0001c0002t0003g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.258+3799T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68881993 | ||||||
chr12:68882002
|
G | A | 1 | a0001c0002t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.258+3790C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882002 | ||||||
chr12:68882024
|
C | CTG | 165 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(162): Show | 166 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.258+3767_258+3768i others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882024 | ||||||
chr12:68882024
|
C | CTGT | 36 | a0001c0001t0001g0142a0001c0001t0001g0188a0001c0001t0001g0193others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.258+3767_258+3768i others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882024 | ||||||
chr12:68882024
|
C | CTT | 31 | a0001c0002t0001g0043a0001c0002t0001g0117a0001c0002t0001g0125others(28): Show | 31 | HG00099.hp2 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.258+3766_258+3767d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882024 | ||||||
chr12:68882025
|
T | TG | 11 | a0001c0001t0001g0167a0001c0001t0001g0222a0001c0001t0024g0216others(8): Show | 11 | HG02129.hp2 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+3766_258+3767i others(3): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882025 | ||||||
chr12:68882026
|
T | G | 9 | a0002c0003t0003g0016a0002c0003t0004g0019a0002c0003t0027g0005others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+3766A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882026 | ||||||
chr12:68882027
|
T | G | 3 | a0002c0003t0019g0026a0002c0003t0032g0335a0002c0003t0033g0336 | 3 | HG02723.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.258+3765A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882027 | ||||||
chr12:68882314
|
C | T | 1 | a0001c0002t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.258+3478G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882314 | ||||||
chr12:68882402
|
CT | C | 86 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(83): Show | 86 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.258+3389delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882402 | ||||||
chr12:68882436
|
T | C | 1 | a0001c0002t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.258+3356A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882436 | ||||||
chr12:68882693
|
T | A | 1 | a0001c0001t0002g0240 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258+3099A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882693 | ||||||
chr12:68882884
|
T | G | 1 | a0002c0009t0001g0311 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.258+2908A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882884 | ||||||
chr12:68882924
|
G | C | 1 | a0001c0007t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.258+2868C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882924 | ||||||
chr12:68882965
|
G | T | 1 | a0001c0001t0056g0196 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.258+2827C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882965 | ||||||
chr12:68882987
|
T | C | 1 | a0001c0002t0001g0191 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.258+2805A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68882987 | ||||||
chr12:68883033
|
C | T | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+2759G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883033 | ||||||
chr12:68883087
|
C | G | 2 | a0001c0002t0031g0050a0002c0003t0003g0033 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.258+2705G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883087 | ||||||
chr12:68883295
|
A | G | 9 | a0002c0003t0003g0016a0002c0003t0004g0019a0002c0003t0027g0005others(6): Show | 9 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.258+2497T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883295 | ||||||
chr12:68883347
|
A | T | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+2445T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883347 | ||||||
chr12:68883385
|
A | G | 242 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.258+2407T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883385 | ||||||
chr12:68883570
|
C | T | 3 | a0002c0003t0029g0018a0002c0003t0032g0335a0002c0003t0033g0336 | 3 | HG00639.hp1 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.258+2222G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883570 | ||||||
chr12:68883666
|
G | T | 232 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.258+2126C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883666 | ||||||
chr12:68883816
|
C | G | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+1976G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883816 | ||||||
chr12:68883820
|
C | T | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+1972G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883820 | ||||||
chr12:68883823
|
G | A | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.258+1969C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883823 | ||||||
chr12:68883884
|
C | T | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.258+1908G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883884 | ||||||
chr12:68883898
|
C | T | 242 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.258+1894G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883898 | ||||||
chr12:68883933
|
T | TA | 87 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(84): Show | 87 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.258+1858dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883933 | ||||||
chr12:68883933
|
TA | T | 139 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.258+1858delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68883933 | ||||||
chr12:68884071
|
T | C | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.258+1721A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884071 | ||||||
chr12:68884110
|
G | GA | 58 | a0001c0002t0001g0040a0001c0002t0001g0048a0001c0002t0001g0073others(55): Show | 58 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.258+1681dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884110 | ||||||
chr12:68884110
|
G | GAA | 41 | a0001c0001t0006g0052a0001c0002t0001g0043a0001c0002t0001g0062others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.258+1680_258+1681d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884110 | ||||||
chr12:68884110
|
G | GAAA | 12 | a0001c0001t0051g0067a0001c0001t0052g0054a0001c0002t0001g0071others(9): Show | 12 | HG00544.hp2 HG01106.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.258+1679_258+1681d others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884110 | ||||||
chr12:68884110
|
GA | G | 126 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0072others(123): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.258+1681delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884110 | ||||||
chr12:68884204
|
C | T | 3 | a0002c0008t0004g0020a0002c0010t0002g0022a0002c0010t0046g0029 | 3 | HG02280.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.258+1588G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884204 | ||||||
chr12:68884263
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0067g0083 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+1529G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884263 | ||||||
chr12:68884425
|
G | A | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.258+1367C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884425 | ||||||
chr12:68884527
|
C | T | 2 | a0001c0002t0001g0097a0001c0002t0001g0106 | 2 | HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.258+1265G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884527 | ||||||
chr12:68884589
|
G | A | 136 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(133): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.258+1203C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884589 | ||||||
chr12:68884710
|
G | C | 10 | a0001c0002t0065g0111a0002c0003t0003g0016a0002c0003t0004g0019others(7): Show | 10 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.258+1082C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884710 | ||||||
chr12:68884977
|
T | C | 49 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(46): Show | 49 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.258+815A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68884977 | ||||||
chr12:68885185
|
T | C | 2 | a0002c0005t0023g0011a0002c0005t0023g0012 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.258+607A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68885185 | ||||||
chr12:68885222
|
G | C | 1 | a0002c0003t0004g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.258+570C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68885222 | ||||||
chr12:68885261
|
G | A | 1 | a0001c0002t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.258+531C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68885261 | ||||||
chr12:68885361
|
G | T | 1 | a0001c0002t0001g0262 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.258+431C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68885361 | ||||||
chr12:68885375
|
G | C | 1 | a0001c0007t0009g0077 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.258+417C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68885375 | ||||||
chr12:68885498
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0067g0083 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.258+294C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 3/8 | chr12 | 68885498 | ||||||
chr12:68885956
|
A | G | 272 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.161-67T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68885956 | ||||||
chr12:68885984
|
C | T | 41 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-95G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68885984 | ||||||
chr12:68886040
|
T | C | 2 | a0001c0002t0065g0111a0002c0003t0030g0030 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.161-151A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886040 | ||||||
chr12:68886326
|
AAC | A | 36 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0143others(33): Show | 36 | HG00099.hp2 HG00438.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.161-439_161-438del others(2): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886326 | ||||||
chr12:68886327
|
AC | A | 141 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.161-439delG | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886327 | ||||||
chr12:68886328
|
C | A | 83 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(80): Show | 83 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.161-439G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886328 | ||||||
chr12:68886371
|
G | A | 272 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.161-482C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886371 | ||||||
chr12:68886489
|
G | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0086others(2): Show | 5 | HG01993.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-600C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886489 | ||||||
chr12:68886492
|
C | T | 30 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(27): Show | 30 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.161-603G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886492 | ||||||
chr12:68886523
|
T | C | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-634A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886523 | ||||||
chr12:68886524
|
C | T | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-635G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886524 | ||||||
chr12:68886554
|
C | G | 34 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(31): Show | 34 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.161-665G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886554 | ||||||
chr12:68886554
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.161-665G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886554 | ||||||
chr12:68886557
|
C | T | 8 | a0001c0002t0007g0095a0001c0004t0008g0233a0002c0003t0004g0023others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-668G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886557 | ||||||
chr12:68886558
|
G | C | 172 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.161-669C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886558 | ||||||
chr12:68886586
|
C | T | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-697G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886586 | ||||||
chr12:68886618
|
C | T | 2 | a0001c0006t0002g0302a0002c0005t0013g0013 | 2 | HG02148.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.161-729G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886618 | ||||||
chr12:68886731
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-842C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886731 | ||||||
chr12:68886739
|
G | A | 41 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-850C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886739 | ||||||
chr12:68886809
|
G | A | 11 | a0001c0002t0065g0111a0002c0003t0003g0016a0002c0003t0004g0019others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-920C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886809 | ||||||
chr12:68886855
|
A | G | 95 | a0001c0001t0001g0096a0001c0001t0001g0108a0001c0001t0001g0156others(92): Show | 95 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.161-966T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886855 | ||||||
chr12:68886933
|
T | C | 276 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.161-1044A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68886933 | ||||||
chr12:68887191
|
C | A | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-1302G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887191 | ||||||
chr12:68887238
|
G | A | 2 | a0001c0002t0065g0111a0002c0003t0030g0030 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.161-1349C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887238 | ||||||
chr12:68887251
|
A | G | 1 | a0001c0002t0060g0100 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.161-1362T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887251 | ||||||
chr12:68887405
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-1516T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887405 | ||||||
chr12:68887577
|
A | C | 13 | a0001c0002t0065g0111a0002c0003t0003g0016a0002c0003t0004g0019others(10): Show | 13 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.161-1688T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887577 | ||||||
chr12:68887795
|
A | C | 41 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-1906T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887795 | ||||||
chr12:68887810
|
G | C | 2 | a0002c0003t0032g0335a0002c0003t0033g0336 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.161-1921C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887810 | ||||||
chr12:68887815
|
C | T | 31 | a0001c0002t0001g0082a0001c0002t0001g0090a0001c0002t0001g0105others(28): Show | 31 | HG00408.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.161-1926G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887815 | ||||||
chr12:68887856
|
G | T | 2 | a0001c0002t0001g0150a0001c0002t0001g0223 | 2 | HG02056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.161-1967C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887856 | ||||||
chr12:68887899
|
T | C | 2 | a0002c0003t0032g0335a0002c0003t0033g0336 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.161-2010A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887899 | ||||||
chr12:68887926
|
C | T | 5 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0086others(2): Show | 5 | HG01993.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-2037G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68887926 | ||||||
chr12:68888415
|
C | T | 7 | a0001c0002t0007g0095a0001c0004t0008g0233a0002c0003t0004g0023others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-2526G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68888415 | ||||||
chr12:68888735
|
C | A | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-2846G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68888735 | ||||||
chr12:68888951
|
A | T | 52 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.161-3062T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68888951 | ||||||
chr12:68889050
|
C | T | 1 | a0001c0007t0003g0126 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.161-3161G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889050 | ||||||
chr12:68889207
|
T | G | 135 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.161-3318A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889207 | ||||||
chr12:68889215
|
A | G | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-3326T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889215 | ||||||
chr12:68889482
|
A | G | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.161-3593T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889482 | ||||||
chr12:68889593
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0248others(2): Show | 5 | NA18612.hp1 NA18944.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-3704G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889593 | ||||||
chr12:68889608
|
T | C | 330 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.161-3719A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889608 | ||||||
chr12:68889738
|
C | T | 1 | a0002c0010t0046g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.161-3849G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889738 | ||||||
chr12:68889820
|
C | T | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-3931G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889820 | ||||||
chr12:68889880
|
C | T | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-3991G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889880 | ||||||
chr12:68889881
|
G | A | 255 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.161-3992C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68889881 | ||||||
chr12:68890090
|
G | A | 1 | a0002c0008t0034g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.161-4201C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890090 | ||||||
chr12:68890141
|
G | T | 2 | a0001c0001t0018g0228a0001c0001t0018g0232 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.161-4252C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890141 | ||||||
chr12:68890195
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02071.hp1 NA18747.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.161-4306G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890195 | ||||||
chr12:68890368
|
TA | T | 42 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-4480delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890368 | ||||||
chr12:68890368
|
TAA | T | 11 | a0001c0002t0065g0111a0002c0003t0003g0016a0002c0003t0004g0019others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-4481_161-4480d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890368 | ||||||
chr12:68890416
|
G | A | 39 | a0001c0002t0001g0082a0001c0002t0001g0090a0001c0002t0001g0105others(36): Show | 39 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.161-4527C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890416 | ||||||
chr12:68890431
|
C | A | 42 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-4542G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890431 | ||||||
chr12:68890488
|
C | T | 272 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.161-4599G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890488 | ||||||
chr12:68890550
|
G | A | 92 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(89): Show | 92 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.161-4661C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890550 | ||||||
chr12:68890601
|
T | TA | 42 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-4713dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890601 | ||||||
chr12:68890878
|
G | A | 1 | a0001c0002t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.161-4989C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68890878 | ||||||
chr12:68891009
|
C | T | 11 | a0001c0002t0065g0111a0002c0003t0003g0016a0002c0003t0004g0019others(8): Show | 11 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-5120G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891009 | ||||||
chr12:68891083
|
C | T | 5 | a0001c0002t0007g0095a0001c0004t0008g0233a0002c0005t0002g0309others(2): Show | 5 | HG02145.hp1 HG03579.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-5194G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891083 | ||||||
chr12:68891154
|
C | T | 3 | a0001c0002t0001g0178a0001c0002t0006g0285a0001c0002t0006g0286 | 3 | HG00741.hp2 HG02258.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.161-5265G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891154 | ||||||
chr12:68891164
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.161-5275T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891164 | ||||||
chr12:68891314
|
T | G | 276 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.161-5425A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891314 | ||||||
chr12:68891367
|
C | G | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-5478G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891367 | ||||||
chr12:68891434
|
G | A | 39 | a0001c0002t0001g0082a0001c0002t0001g0090a0001c0002t0001g0105others(36): Show | 39 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.161-5545C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891434 | ||||||
chr12:68891455
|
C | T | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-5566G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891455 | ||||||
chr12:68891641
|
A | G | 276 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.161-5752T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891641 | ||||||
chr12:68891734
|
T | G | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.161-5845A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891734 | ||||||
chr12:68891886
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0217 | 2 | HG02074.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.161-5997C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68891886 | ||||||
chr12:68892109
|
G | A | 2 | a0001c0004t0017g0102a0001c0004t0017g0103 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.161-6220C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892109 | ||||||
chr12:68892331
|
G | A | 1 | a0002c0003t0019g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-6442C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892331 | ||||||
chr12:68892537
|
G | T | 40 | a0001c0001t0006g0052a0001c0001t0051g0067a0001c0001t0052g0054others(37): Show | 40 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.161-6648C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892537 | ||||||
chr12:68892548
|
A | G | 1 | a0001c0001t0004g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161-6659T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892548 | ||||||
chr12:68892554
|
T | C | 5 | a0001c0002t0007g0095a0001c0004t0008g0233a0002c0005t0002g0309others(2): Show | 5 | HG02145.hp1 HG03579.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6665A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892554 | ||||||
chr12:68892634
|
C | T | 2 | a0004c0013t0004g0027a0006c0015t0041g0301 | 2 | HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-6745G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892634 | ||||||
chr12:68892696
|
C | T | 1 | a0002c0003t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-6807G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892696 | ||||||
chr12:68892720
|
G | A | 4 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | NA18949.hp1 NA18971.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-6831C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892720 | ||||||
chr12:68892800
|
A | G | 1 | a0002c0008t0004g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161-6911T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892800 | ||||||
chr12:68892879
|
G | A | 2 | a0001c0002t0001g0191a0001c0002t0001g0258 | 2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.161-6990C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68892879 | ||||||
chr12:68893096
|
G | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0086others(2): Show | 5 | HG01993.hp1 HG02698.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-7207C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893096 | ||||||
chr12:68893149
|
C | CA | 47 | a0001c0002t0001g0082a0001c0002t0001g0090a0001c0002t0001g0105others(44): Show | 47 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.161-7261dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893149 | ||||||
chr12:68893149
|
C | CAA | 211 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.161-7262_161-7261d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893149 | ||||||
chr12:68893149
|
C | CAAA | 11 | a0001c0001t0003g0239a0001c0001t0004g0229a0001c0001t0004g0298others(8): Show | 11 | HG00735.hp1 HG01496.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-7263_161-7261d others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893149 | ||||||
chr12:68893201
|
G | A | 336 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(333): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.161-7312C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893201 | ||||||
chr12:68893285
|
G | C | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.161-7396C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893285 | ||||||
chr12:68893340
|
T | C | 1 | a0001c0006t0039g0182 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.161-7451A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893340 | ||||||
chr12:68893435
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.161-7546A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893435 | ||||||
chr12:68893482
|
C | G | 1 | a0001c0002t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.161-7593G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893482 | ||||||
chr12:68893680
|
C | G | 1 | a0002c0003t0003g0015 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.161-7791G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893680 | ||||||
chr12:68893845
|
G | A | 1 | a0001c0001t0014g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.161-7956C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893845 | ||||||
chr12:68893855
|
G | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0207a0001c0001t0001g0277others(1): Show | 4 | HG00280.hp2 HG01496.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-7966C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893855 | ||||||
chr12:68893903
|
C | G | 10 | a0001c0002t0065g0111a0002c0003t0003g0016a0002c0003t0004g0019others(7): Show | 10 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-8014G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893903 | ||||||
chr12:68893965
|
C | T | 150 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(147): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.161-8076G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68893965 | ||||||
chr12:68894018
|
G | A | 4 | a0001c0001t0004g0229a0001c0001t0004g0298a0001c0001t0018g0228others(1): Show | 4 | HG02896.hp1 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-8129C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894018 | ||||||
chr12:68894048
|
C | T | 1 | a0001c0002t0065g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-8159G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894048 | ||||||
chr12:68894229
|
C | G | 14 | a0001c0002t0001g0090a0001c0002t0001g0105a0001c0002t0001g0107others(11): Show | 14 | HG02015.hp2 HG02071.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-8340G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894229 | ||||||
chr12:68894307
|
C | A | 2 | a0002c0005t0023g0011a0002c0005t0023g0012 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.161-8418G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894307 | ||||||
chr12:68894375
|
G | A | 1 | a0001c0002t0006g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-8486C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894375 | ||||||
chr12:68894397
|
C | T | 1 | a0002c0003t0025g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-8508G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894397 | ||||||
chr12:68894556
|
A | G | 1 | a0001c0007t0002g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.161-8667T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894556 | ||||||
chr12:68894586
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.161-8697G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894586 | ||||||
chr12:68894716
|
G | A | 1 | a0001c0007t0042g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.161-8827C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894716 | ||||||
chr12:68894773
|
G | A | 1 | a0001c0002t0031g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-8884C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894773 | ||||||
chr12:68894777
|
G | A | 2 | a0002c0009t0002g0031a0002c0009t0002g0032 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161-8888C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894777 | ||||||
chr12:68894844
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161-8955C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894844 | ||||||
chr12:68894986
|
A | AC | 6 | a0001c0002t0001g0191a0001c0002t0001g0258a0001c0002t0002g0086others(3): Show | 6 | HG01993.hp1 HG02602.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-9098dupG | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68894986 | ||||||
chr12:68895028
|
C | CA | 126 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0074others(123): Show | 127 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.161-9140dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895028 | ||||||
chr12:68895028
|
C | CAA | 9 | a0001c0001t0001g0180a0001c0001t0001g0186a0001c0001t0001g0189others(6): Show | 9 | HG00280.hp2 HG00733.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-9141_161-9140d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895028 | ||||||
chr12:68895028
|
CA | C | 49 | a0001c0002t0001g0082a0001c0002t0001g0090a0001c0002t0001g0107others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.161-9140delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895028 | ||||||
chr12:68895088
|
G | C | 13 | a0001c0002t0048g0287a0001c0002t0068g0299a0001c0004t0012g0300others(10): Show | 13 | HG01109.hp2 HG02717.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-9199C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895088 | ||||||
chr12:68895116
|
T | A | 2 | a0001c0002t0065g0111a0002c0003t0030g0030 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.161-9227A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895116 | ||||||
chr12:68895178
|
A | G | 125 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0143others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.161-9289T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895178 | ||||||
chr12:68895213
|
G | A | 2 | a0001c0001t0001g0277a0002c0008t0001g0312 | 2 | HG01496.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.161-9324C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895213 | ||||||
chr12:68895269
|
C | A | 13 | a0001c0002t0048g0287a0001c0002t0068g0299a0001c0004t0012g0300others(10): Show | 13 | HG01109.hp2 HG02717.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-9380G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895269 | ||||||
chr12:68895323
|
T | G | 2 | a0001c0001t0066g0256a0001c0004t0012g0162 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.161-9434A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895323 | ||||||
chr12:68895387
|
C | T | 1 | a0001c0002t0048g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.161-9498G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895387 | ||||||
chr12:68895622
|
C | T | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-9733G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895622 | ||||||
chr12:68895745
|
C | T | 8 | a0001c0002t0007g0095a0002c0003t0004g0023a0002c0003t0019g0026others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-9856G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895745 | ||||||
chr12:68895925
|
A | T | 3 | a0002c0005t0002g0309a0002c0005t0002g0310a0002c0005t0002g0323 | 3 | HG02145.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.161-10036T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895925 | ||||||
chr12:68895969
|
A | C | 61 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0142others(58): Show | 61 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.161-10080T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895969 | ||||||
chr12:68895976
|
C | T | 1 | a0002c0003t0007g0322 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-10087G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895976 | ||||||
chr12:68895986
|
T | C | 129 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0072others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.161-10097A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895986 | ||||||
chr12:68895995
|
C | T | 176 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0072others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.161-10106G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68895995 | ||||||
chr12:68896076
|
C | T | 6 | a0001c0001t0004g0203a0001c0006t0008g0226a0001c0006t0008g0244others(3): Show | 6 | HG01167.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-10187G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896076 | ||||||
chr12:68896393
|
G | GT | 29 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(26): Show | 29 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-10505dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896393 | ||||||
chr12:68896627
|
C | G | 1 | a0002c0009t0001g0311 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.161-10738G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896627 | ||||||
chr12:68896795
|
T | C | 1 | a0002c0003t0003g0315 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-10906A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896795 | ||||||
chr12:68896893
|
G | T | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-11004C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896893 | ||||||
chr12:68896902
|
G | T | 96 | a0001c0001t0001g0060a0001c0001t0004g0298a0001c0001t0006g0052others(93): Show | 96 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.161-11013C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896902 | ||||||
chr12:68896910
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.161-11021A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896910 | ||||||
chr12:68896912
|
GA | G | 8 | a0002c0003t0003g0016a0002c0003t0019g0026a0002c0003t0027g0005others(5): Show | 8 | HG01167.hp1 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-11024delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896912 | ||||||
chr12:68896965
|
T | C | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-11076A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68896965 | ||||||
chr12:68897246
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.161-11357T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897246 | ||||||
chr12:68897271
|
G | GT | 9 | a0001c0001t0001g0096a0001c0002t0001g0153a0001c0002t0001g0172others(6): Show | 9 | HG00423.hp2 HG00621.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-11383dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897271 | ||||||
chr12:68897450
|
G | A | 1 | a0001c0002t0010g0293 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.161-11561C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897450 | ||||||
chr12:68897508
|
T | C | 143 | a0001c0001t0001g0060a0001c0001t0001g0072a0001c0001t0001g0094others(140): Show | 143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.161-11619A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897508 | ||||||
chr12:68897565
|
G | A | 1 | a0001c0002t0001g0174 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.161-11676C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897565 | ||||||
chr12:68897598
|
G | A | 1 | a0002c0003t0025g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-11709C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897598 | ||||||
chr12:68897638
|
T | C | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-11749A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897638 | ||||||
chr12:68897639
|
G | C | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-11750C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897639 | ||||||
chr12:68897666
|
A | G | 101 | a0001c0001t0001g0060a0001c0001t0004g0298a0001c0001t0006g0052others(98): Show | 101 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.161-11777T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897666 | ||||||
chr12:68897691
|
C | T | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-11802G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897691 | ||||||
chr12:68897705
|
C | G | 3 | a0001c0002t0004g0246a0001c0002t0031g0050a0002c0003t0003g0033 | 3 | HG02055.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.161-11816G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897705 | ||||||
chr12:68897715
|
T | C | 3 | a0002c0003t0027g0005a0002c0005t0022g0326a0002c0008t0025g0024 | 3 | HG02809.hp2 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.161-11826A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897715 | ||||||
chr12:68897721
|
A | G | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-11832T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897721 | ||||||
chr12:68897724
|
G | A | 33 | a0001c0001t0001g0072a0001c0001t0001g0137a0001c0001t0001g0142others(30): Show | 33 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-11835C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897724 | ||||||
chr12:68897731
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.161-11842G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897731 | ||||||
chr12:68897736
|
C | CA | 14 | a0001c0001t0067g0083a0001c0002t0001g0153a0001c0002t0007g0247others(11): Show | 14 | HG01167.hp1 HG01433.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-11848dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897736 | ||||||
chr12:68897736
|
CA | C | 130 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0074others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.161-11848delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897736 | ||||||
chr12:68897736
|
CAA | C | 19 | a0001c0001t0004g0298a0001c0002t0007g0095a0001c0002t0048g0287others(16): Show | 19 | HG01109.hp2 HG02145.hp2 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.161-11849_161-1184 others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897736 | ||||||
chr12:68897882
|
C | T | 1 | a0002c0003t0027g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.161-11993G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897882 | ||||||
chr12:68897883
|
G | A | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-11994C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897883 | ||||||
chr12:68897995
|
C | A | 1 | a0001c0002t0006g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.161-12106G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68897995 | ||||||
chr12:68898018
|
A | AT | 33 | a0001c0001t0001g0080a0001c0001t0001g0098a0001c0001t0001g0171others(30): Show | 33 | HG01358.hp1 HG01361.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-12130dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898018 | ||||||
chr12:68898035
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.161-12146C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898035 | ||||||
chr12:68898129
|
C | T | 18 | a0001c0001t0004g0298a0001c0002t0048g0287a0001c0002t0068g0299others(15): Show | 18 | HG01109.hp2 HG02145.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.161-12240G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898129 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1110): Show |
1 | a0001c0001t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1121): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1124): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0221 | 2 | HG02273.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.161-12260_161-1225 others(1135): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1124): Show |
2 | a0001c0001t0001g0158a0001c0001t0001g0206 | 2 | HG00558.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.161-12260_161-1225 others(1135): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1126): Show |
1 | a0001c0001t0001g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1137): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1111): Show |
1 | a0001c0001t0001g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1122): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1126): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0204 | 2 | HG02293.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.161-12260_161-1225 others(1137): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1127): Show |
1 | a0001c0001t0001g0212 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1138): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1127): Show |
1 | a0001c0001t0001g0168 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1138): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1132): Show |
1 | a0001c0001t0001g0170 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1143): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898148
|
C | CTGGCCTG others(1133): Show |
1 | a0001c0001t0001g0167 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.161-12260_161-1225 others(1144): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898148 | ||||||
chr12:68898183
|
A | T | 3 | a0002c0003t0003g0015a0002c0005t0013g0009a0002c0005t0013g0010 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.161-12294T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898183 | ||||||
chr12:68898266
|
C | A | 1 | a0002c0003t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.161-12377G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898266 | ||||||
chr12:68898400
|
G | C | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-12511C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898400 | ||||||
chr12:68898499
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.161-12610G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898499 | ||||||
chr12:68898559
|
T | G | 2 | a0002c0009t0002g0031a0002c0009t0002g0032 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161-12670A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898559 | ||||||
chr12:68898599
|
A | C | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-12710T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898599 | ||||||
chr12:68898668
|
T | A | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161-12779A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898668 | ||||||
chr12:68898681
|
A | G | 8 | a0001c0001t0001g0230a0001c0001t0004g0229a0001c0001t0018g0228others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-12792T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898681 | ||||||
chr12:68898725
|
T | C | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-12836A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898725 | ||||||
chr12:68898944
|
C | T | 1 | a0001c0002t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.161-13055G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68898944 | ||||||
chr12:68899648
|
A | C | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13759T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899648 | ||||||
chr12:68899649
|
T | A | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13760A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899649 | ||||||
chr12:68899650
|
A | C | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13761T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899650 | ||||||
chr12:68899652
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13763C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899652 | ||||||
chr12:68899653
|
A | G | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13764T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899653 | ||||||
chr12:68899661
|
A | G | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13772T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899661 | ||||||
chr12:68899662
|
A | T | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13773T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899662 | ||||||
chr12:68899663
|
T | G | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13774A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899663 | ||||||
chr12:68899664
|
G | T | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13775C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899664 | ||||||
chr12:68899665
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.161-13776G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899665 | ||||||
chr12:68899848
|
A | C | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-13959T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899848 | ||||||
chr12:68899889
|
C | T | 5 | a0002c0003t0004g0023a0002c0003t0028g0006a0002c0003t0030g0030others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-14000G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68899889 | ||||||
chr12:68900201
|
A | C | 1 | a0001c0002t0065g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-14312T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900201 | ||||||
chr12:68900326
|
A | G | 1 | a0001c0002t0009g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.161-14437T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900326 | ||||||
chr12:68900385
|
C | T | 1 | a0001c0002t0065g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-14496G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900385 | ||||||
chr12:68900558
|
C | T | 269 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.161-14669G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900558 | ||||||
chr12:68900625
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.161-14736T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900625 | ||||||
chr12:68900816
|
A | G | 98 | a0001c0001t0001g0060a0001c0001t0004g0298a0001c0001t0006g0052others(95): Show | 98 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-14927T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900816 | ||||||
chr12:68900970
|
T | G | 3 | a0002c0003t0003g0016a0002c0003t0019g0026a0002c0010t0008g0025 | 3 | HG01167.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.161-15081A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68900970 | ||||||
chr12:68901003
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.161-15114G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68901003 | ||||||
chr12:68901237
|
C | A | 2 | a0002c0009t0002g0031a0002c0009t0002g0032 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161-15348G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68901237 | ||||||
chr12:68901304
|
C | T | 3 | a0002c0003t0003g0015a0002c0005t0013g0009a0002c0005t0013g0010 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.161-15415G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68901304 | ||||||
chr12:68901363
|
G | A | 3 | a0002c0003t0003g0016a0002c0003t0019g0026a0002c0010t0008g0025 | 3 | HG01167.hp1 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.161-15474C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68901363 | ||||||
chr12:68901899
|
G | A | 8 | a0001c0002t0007g0095a0002c0003t0003g0328a0002c0003t0015g0329others(5): Show | 8 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-16010C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68901899 | ||||||
chr12:68902125
|
G | A | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-16236C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902125 | ||||||
chr12:68902302
|
A | T | 3 | a0001c0001t0002g0260a0001c0001t0006g0259a0001c0002t0001g0249 | 3 | NA18944.hp1 NA18980.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.161-16413T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902302 | ||||||
chr12:68902605
|
T | C | 4 | a0001c0002t0001g0064a0001c0002t0001g0065a0001c0002t0001g0068others(1): Show | 4 | NA18946.hp1 NA18991.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-16716A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902605 | ||||||
chr12:68902735
|
C | T | 1 | a0002c0010t0002g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-16846G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902735 | ||||||
chr12:68902740
|
T | C | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-16851A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902740 | ||||||
chr12:68902775
|
C | T | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.161-16886G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902775 | ||||||
chr12:68902776
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0014g0291 | 2 | HG01099.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.161-16887C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902776 | ||||||
chr12:68902933
|
C | T | 42 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-17044G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902933 | ||||||
chr12:68902938
|
T | C | 69 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.161-17049A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68902938 | ||||||
chr12:68903051
|
T | C | 1 | a0001c0007t0042g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.161-17162A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903051 | ||||||
chr12:68903327
|
C | T | 7 | a0002c0003t0003g0328a0002c0003t0015g0329a0002c0003t0015g0330others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-17438G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903327 | ||||||
chr12:68903392
|
T | C | 2 | a0001c0002t0010g0292a0001c0002t0010g0293 | 2 | NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.161-17503A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903392 | ||||||
chr12:68903467
|
C | T | 2 | a0002c0009t0002g0031a0002c0009t0002g0032 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161-17578G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903467 | ||||||
chr12:68903531
|
A | C | 47 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-17642T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903531 | ||||||
chr12:68903694
|
T | C | 7 | a0002c0003t0003g0328a0002c0003t0015g0329a0002c0003t0015g0330others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-17805A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903694 | ||||||
chr12:68903824
|
C | T | 57 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(54): Show | 57 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.161-17935G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903824 | ||||||
chr12:68903879
|
A | ATTCT | 75 | a0001c0001t0001g0060a0001c0001t0001g0207a0001c0001t0001g0234others(72): Show | 75 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.161-17994_161-1799 others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903879 | ||||||
chr12:68903879
|
A | ATTCTTTC others(1): Show |
7 | a0002c0003t0003g0315a0002c0003t0004g0314a0002c0005t0005g0014others(4): Show | 7 | HG02486.hp1 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-17998_161-1799 others(12): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903879 | ||||||
chr12:68903879
|
A | ATTCTTTC others(5): Show |
1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-18002_161-1799 others(16): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68903879 | ||||||
chr12:68904100
|
A | G | 7 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(4): Show | 7 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-18211T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904100 | ||||||
chr12:68904138
|
T | G | 5 | a0002c0003t0019g0026a0002c0003t0057g0008a0002c0008t0025g0024others(2): Show | 5 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-18249A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904138 | ||||||
chr12:68904280
|
T | C | 1 | a0001c0007t0001g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.161-18391A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904280 | ||||||
chr12:68904282
|
G | A | 1 | a0001c0001t0004g0229 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-18393C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904282 | ||||||
chr12:68904315
|
T | C | 1 | a0001c0002t0001g0294 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.161-18426A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904315 | ||||||
chr12:68904323
|
T | C | 6 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(3): Show | 6 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-18434A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904323 | ||||||
chr12:68904468
|
T | A | 1 | a0001c0001t0055g0305 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.161-18579A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904468 | ||||||
chr12:68904597
|
A | G | 5 | a0002c0003t0019g0026a0002c0003t0057g0008a0002c0008t0025g0024others(2): Show | 5 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-18708T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904597 | ||||||
chr12:68904767
|
A | G | 12 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(9): Show | 12 | HG01167.hp1 HG01361.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-18878T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904767 | ||||||
chr12:68904915
|
GT | G | 42 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-19027delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904915 | ||||||
chr12:68904923
|
G | A | 10 | a0002c0003t0003g0015a0002c0003t0003g0328a0002c0003t0015g0329others(7): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.161-19034C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904923 | ||||||
chr12:68904948
|
G | A | 5 | a0002c0003t0004g0023a0002c0003t0027g0005a0002c0003t0028g0006others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-19059C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904948 | ||||||
chr12:68904953
|
C | T | 47 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-19064G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68904953 | ||||||
chr12:68905018
|
C | A | 1 | a0002c0010t0002g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-19129G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905018 | ||||||
chr12:68905034
|
G | A | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-19145C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905034 | ||||||
chr12:68905157
|
G | A | 57 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(54): Show | 57 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.161-19268C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905157 | ||||||
chr12:68905172
|
G | C | 6 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(3): Show | 6 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-19283C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905172 | ||||||
chr12:68905175
|
G | C | 4 | a0002c0003t0025g0007a0002c0003t0029g0018a0002c0005t0023g0011others(1): Show | 4 | HG00639.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-19286C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905175 | ||||||
chr12:68905212
|
AATAT | A | 5 | a0002c0008t0004g0020a0002c0010t0002g0022a0002c0010t0046g0029others(2): Show | 5 | HG02280.hp2 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-19327_161-1932 others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905212 | ||||||
chr12:68905240
|
A | T | 57 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(54): Show | 57 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.161-19351T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905240 | ||||||
chr12:68905318
|
T | C | 6 | a0002c0003t0003g0016a0002c0003t0019g0026a0002c0003t0057g0008others(3): Show | 6 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-19429A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905318 | ||||||
chr12:68905481
|
A | C | 2 | a0001c0002t0010g0292a0001c0002t0010g0293 | 2 | NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.161-19592T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905481 | ||||||
chr12:68905691
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.161-19802G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905691 | ||||||
chr12:68905824
|
T | C | 1 | a0001c0002t0006g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-19935A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68905824 | ||||||
chr12:68906065
|
C | T | 2 | a0002c0009t0002g0031a0002c0009t0002g0032 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.161-20176G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906065 | ||||||
chr12:68906130
|
C | T | 3 | a0001c0007t0009g0075a0001c0007t0009g0076a0001c0007t0009g0077 | 3 | HG01109.hp1 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.161-20241G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906130 | ||||||
chr12:68906285
|
C | A | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-20396G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906285 | ||||||
chr12:68906291
|
C | A | 69 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.161-20402G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906291 | ||||||
chr12:68906291
|
C | T | 2 | a0002c0003t0003g0315a0002c0003t0004g0314 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.161-20402G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906291 | ||||||
chr12:68906292
|
C | A | 69 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.161-20403G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906292 | ||||||
chr12:68906312
|
G | A | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-20423C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906312 | ||||||
chr12:68906392
|
A | G | 1 | a0001c0002t0001g0271 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.161-20503T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906392 | ||||||
chr12:68906495
|
G | GT | 60 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(57): Show | 60 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.161-20607dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906495 | ||||||
chr12:68906501
|
T | A | 2 | a0002c0003t0057g0008a0002c0009t0044g0021 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.161-20612A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906501 | ||||||
chr12:68906567
|
G | A | 42 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-20678C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906567 | ||||||
chr12:68906637
|
C | A | 2 | a0002c0003t0003g0328a0003c0012t0007g0334 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.161-20748G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906637 | ||||||
chr12:68906762
|
C | T | 10 | a0002c0003t0003g0015a0002c0003t0003g0328a0002c0003t0015g0329others(7): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.161-20873G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906762 | ||||||
chr12:68906774
|
T | C | 1 | a0002c0005t0002g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161-20885A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906774 | ||||||
chr12:68906805
|
C | T | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-20916G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68906805 | ||||||
chr12:68907087
|
C | T | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-21198G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907087 | ||||||
chr12:68907122
|
C | A | 42 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-21233G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907122 | ||||||
chr12:68907310
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.161-21421G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907310 | ||||||
chr12:68907386
|
TAA | T | 42 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.161-21499_161-2149 others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907386 | ||||||
chr12:68907507
|
T | C | 47 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(44): Show | 47 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-21618A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907507 | ||||||
chr12:68907627
|
G | A | 1 | a0002c0005t0002g0323 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-21738C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907627 | ||||||
chr12:68907694
|
G | A | 6 | a0002c0003t0003g0016a0002c0003t0019g0026a0002c0003t0057g0008others(3): Show | 6 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-21805C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907694 | ||||||
chr12:68907818
|
G | GTTAT | 4 | a0002c0003t0025g0007a0002c0003t0029g0018a0002c0005t0023g0011others(1): Show | 4 | HG00639.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-21933_161-2193 others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907818 | ||||||
chr12:68907818
|
G | GTTATTTA others(5): Show |
38 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.161-21941_161-2193 others(16): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68907818 | ||||||
chr12:68908017
|
C | T | 10 | a0002c0003t0003g0015a0002c0003t0003g0328a0002c0003t0015g0329others(7): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.161-22128G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908017 | ||||||
chr12:68908241
|
G | C | 2 | a0002c0003t0004g0023a0002c0003t0028g0006 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-22352C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908241 | ||||||
chr12:68908309
|
C | G | 6 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(3): Show | 6 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-22420G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908309 | ||||||
chr12:68908327
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161-22438G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908327 | ||||||
chr12:68908396
|
C | CT | 9 | a0001c0002t0001g0115a0001c0002t0007g0095a0001c0004t0005g0145others(6): Show | 9 | HG00642.hp2 HG01361.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-22508dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908396 | ||||||
chr12:68908396
|
CT | C | 16 | a0001c0001t0001g0129a0001c0001t0001g0140a0001c0001t0001g0176others(13): Show | 16 | HG00621.hp2 HG02273.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.161-22508delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908396 | ||||||
chr12:68908432
|
C | T | 1 | a0001c0002t0001g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161-22543G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908432 | ||||||
chr12:68908460
|
C | A | 1 | a0001c0002t0003g0104 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.161-22571G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908460 | ||||||
chr12:68908532
|
C | T | 10 | a0002c0003t0003g0015a0002c0003t0003g0328a0002c0003t0015g0329others(7): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.161-22643G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908532 | ||||||
chr12:68908733
|
G | A | 6 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(3): Show | 6 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-22844C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908733 | ||||||
chr12:68908770
|
C | T | 6 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(3): Show | 6 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-22881G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908770 | ||||||
chr12:68908771
|
G | A | 7 | a0002c0003t0003g0328a0002c0003t0015g0329a0002c0003t0015g0330others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-22882C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908771 | ||||||
chr12:68908893
|
T | C | 10 | a0002c0003t0003g0015a0002c0003t0003g0328a0002c0003t0015g0329others(7): Show | 10 | HG02145.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.161-23004A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908893 | ||||||
chr12:68908901
|
C | T | 3 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103 | 3 | HG01361.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.161-23012G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908901 | ||||||
chr12:68908992
|
T | C | 3 | a0002c0003t0004g0023a0002c0003t0028g0006a0002c0003t0030g0030 | 3 | HG02451.hp1 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-23103A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908992 | ||||||
chr12:68908996
|
T | C | 6 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103others(3): Show | 6 | HG01361.hp2 HG02145.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-23107A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68908996 | ||||||
chr12:68909227
|
G | A | 5 | a0002c0003t0004g0023a0002c0003t0027g0005a0002c0003t0028g0006others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-23338C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909227 | ||||||
chr12:68909318
|
T | G | 64 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0137others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.160+23360A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909318 | ||||||
chr12:68909374
|
A | AT | 6 | a0001c0002t0001g0115a0002c0003t0019g0026a0002c0003t0057g0008others(3): Show | 6 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+23303dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909374 | ||||||
chr12:68909445
|
C | T | 230 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(227): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.160+23233G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909445 | ||||||
chr12:68909478
|
T | C | 1 | a0001c0002t0002g0086 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.160+23200A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909478 | ||||||
chr12:68909484
|
T | G | 211 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(208): Show | 212 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.160+23194A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909484 | ||||||
chr12:68909567
|
C | T | 1 | a0001c0002t0001g0037 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.160+23111G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909567 | ||||||
chr12:68909650
|
T | G | 1 | a0001c0001t0055g0305 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160+23028A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909650 | ||||||
chr12:68909691
|
T | C | 1 | a0001c0007t0002g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.160+22987A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909691 | ||||||
chr12:68909838
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.160+22840C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909838 | ||||||
chr12:68909839
|
G | A | 1 | a0001c0002t0006g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.160+22839C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909839 | ||||||
chr12:68909841
|
G | T | 4 | a0002c0003t0003g0315a0002c0003t0004g0314a0002c0005t0023g0011others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+22837C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909841 | ||||||
chr12:68909843
|
G | T | 1 | a0003c0012t0007g0334 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+22835C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909843 | ||||||
chr12:68909851
|
C | G | 3 | a0002c0003t0007g0317a0002c0003t0019g0026a0002c0010t0008g0025 | 3 | HG01167.hp1 HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.160+22827G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909851 | ||||||
chr12:68909860
|
T | G | 1 | a0002c0003t0004g0023 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.160+22818A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909860 | ||||||
chr12:68909862
|
A | G | 159 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0109others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.160+22816T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909862 | ||||||
chr12:68909867
|
A | G | 4 | a0001c0001t0001g0080a0001c0002t0001g0079a0001c0002t0003g0104others(1): Show | 4 | NA18947.hp2 NA18963.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+22811T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909867 | ||||||
chr12:68909873
|
A | T | 3 | a0001c0001t0001g0248a0001c0001t0001g0281a0001c0002t0062g0280 | 3 | NA18968.hp1 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.160+22805T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909873 | ||||||
chr12:68909876
|
A | C | 1 | a0001c0001t0004g0229 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+22802T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909876 | ||||||
chr12:68909892
|
G | A | 4 | a0001c0004t0005g0154a0001c0007t0009g0075a0001c0007t0009g0076others(1): Show | 4 | HG01081.hp1 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+22786C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909892 | ||||||
chr12:68909905
|
C | G | 1 | a0002c0005t0035g0017 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160+22773G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909905 | ||||||
chr12:68909905
|
C | T | 64 | a0001c0001t0001g0060a0001c0001t0001g0072a0001c0001t0001g0137others(61): Show | 64 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.160+22773G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909905 | ||||||
chr12:68909908
|
C | G | 142 | a0001c0001t0001g0074a0001c0001t0001g0096a0001c0001t0001g0109others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.160+22770G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909908 | ||||||
chr12:68909915
|
C | G | 2 | a0001c0007t0001g0132a0002c0008t0025g0024 | 2 | HG01516.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.160+22763G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909915 | ||||||
chr12:68909924
|
A | G | 5 | a0001c0001t0001g0263a0001c0001t0003g0265a0001c0002t0002g0264others(2): Show | 5 | HG01071.hp1 HG01346.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+22754T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909924 | ||||||
chr12:68909965
|
A | C | 3 | a0001c0002t0007g0095a0001c0004t0017g0102a0001c0004t0017g0103 | 3 | HG01361.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.160+22713T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68909965 | ||||||
chr12:68910221
|
T | C | 1 | a0001c0006t0002g0302 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.160+22457A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910221 | ||||||
chr12:68910246
|
G | T | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+22432C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910246 | ||||||
chr12:68910414
|
T | C | 6 | a0001c0001t0001g0205a0001c0001t0002g0260a0001c0001t0006g0259others(3): Show | 6 | NA18944.hp1 NA18967.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+22264A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910414 | ||||||
chr12:68910451
|
T | C | 1 | a0001c0002t0001g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+22227A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910451 | ||||||
chr12:68910459
|
C | A | 15 | a0002c0003t0003g0016a0002c0003t0004g0023a0002c0003t0019g0026others(12): Show | 15 | HG01167.hp1 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+22219G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910459 | ||||||
chr12:68910790
|
C | T | 1 | a0002c0003t0025g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+21888G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910790 | ||||||
chr12:68910968
|
A | T | 42 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(39): Show | 42 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.160+21710T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68910968 | ||||||
chr12:68911058
|
C | T | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+21620G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911058 | ||||||
chr12:68911093
|
A | G | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+21585T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911093 | ||||||
chr12:68911509
|
G | A | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+21169C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911509 | ||||||
chr12:68911517
|
A | AT | 23 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(20): Show | 23 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+21160dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911517 | ||||||
chr12:68911622
|
C | T | 1 | a0001c0002t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.160+21056G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911622 | ||||||
chr12:68911678
|
T | C | 274 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(271): Show | 275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.160+21000A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911678 | ||||||
chr12:68911710
|
G | A | 5 | a0002c0003t0007g0317a0002c0003t0007g0320a0002c0003t0007g0322others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+20968C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911710 | ||||||
chr12:68911726
|
T | C | 3 | a0002c0003t0004g0019a0002c0005t0016g0003a0002c0005t0016g0004 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.160+20952A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911726 | ||||||
chr12:68911806
|
G | A | 8 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0248others(5): Show | 8 | HG02523.hp2 NA18612.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+20872C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911806 | ||||||
chr12:68911808
|
G | A | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+20870C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911808 | ||||||
chr12:68911914
|
C | T | 24 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0137others(21): Show | 24 | HG00408.hp1 HG00438.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+20764G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68911914 | ||||||
chr12:68912003
|
G | GTAT | 23 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(20): Show | 23 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+20672_160+2067 others(7): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912003 | ||||||
chr12:68912039
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.160+20639G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912039 | ||||||
chr12:68912057
|
G | A | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+20621C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912057 | ||||||
chr12:68912121
|
C | A | 49 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(46): Show | 49 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.160+20557G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912121 | ||||||
chr12:68912200
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.160+20478G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912200 | ||||||
chr12:68912444
|
A | T | 4 | a0001c0001t0053g0243a0001c0006t0012g0225a0001c0006t0012g0241others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+20234T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912444 | ||||||
chr12:68912600
|
G | C | 1 | a0001c0002t0001g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.160+20078C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912600 | ||||||
chr12:68912717
|
C | T | 1 | a0001c0007t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.160+19961G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912717 | ||||||
chr12:68912873
|
T | G | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+19805A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68912873 | ||||||
chr12:68913035
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160+19643C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913035 | ||||||
chr12:68913070
|
C | G | 1 | a0001c0002t0001g0157 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.160+19608G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913070 | ||||||
chr12:68913151
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.160+19527C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913151 | ||||||
chr12:68913201
|
C | T | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+19477G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913201 | ||||||
chr12:68913329
|
G | C | 3 | a0002c0003t0003g0033a0002c0009t0002g0031a0002c0009t0002g0032 | 3 | HG02809.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160+19349C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913329 | ||||||
chr12:68913356
|
T | G | 41 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(38): Show | 41 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.160+19322A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913356 | ||||||
chr12:68913412
|
C | T | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+19266G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913412 | ||||||
chr12:68913551
|
T | C | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+19127A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913551 | ||||||
chr12:68913590
|
C | G | 39 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(36): Show | 39 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.160+19088G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913590 | ||||||
chr12:68913687
|
G | A | 4 | a0001c0002t0001g0278a0001c0002t0003g0146a0001c0004t0005g0273others(1): Show | 4 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+18991C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913687 | ||||||
chr12:68913739
|
C | A | 39 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(36): Show | 39 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.160+18939G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913739 | ||||||
chr12:68913750
|
G | A | 1 | a0001c0007t0002g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.160+18928C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913750 | ||||||
chr12:68913788
|
G | A | 41 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(38): Show | 41 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.160+18890C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68913788 | ||||||
chr12:68914013
|
T | C | 2 | a0002c0003t0003g0328a0003c0012t0007g0334 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.160+18665A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914013 | ||||||
chr12:68914035
|
T | C | 1 | a0002c0005t0002g0310 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.160+18643A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914035 | ||||||
chr12:68914044
|
C | T | 3 | a0001c0002t0004g0246a0001c0002t0007g0247a0001c0002t0031g0050 | 3 | HG02055.hp2 HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.160+18634G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914044 | ||||||
chr12:68914322
|
T | A | 1 | a0002c0003t0015g0332 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.160+18356A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914322 | ||||||
chr12:68914411
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160+18267A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914411 | ||||||
chr12:68914429
|
C | T | 1 | a0001c0004t0011g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.160+18249G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914429 | ||||||
chr12:68914905
|
T | C | 1 | a0002c0003t0004g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.160+17773A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68914905 | ||||||
chr12:68915163
|
C | T | 1 | a0002c0003t0003g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.160+17515G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915163 | ||||||
chr12:68915424
|
G | A | 1 | a0001c0001t0004g0112 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160+17254C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915424 | ||||||
chr12:68915558
|
T | G | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+17120A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915558 | ||||||
chr12:68915579
|
A | C | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+17099T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915579 | ||||||
chr12:68915597
|
A | G | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+17081T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915597 | ||||||
chr12:68915665
|
C | T | 42 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(39): Show | 42 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.160+17013G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915665 | ||||||
chr12:68915682
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.160+16996T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915682 | ||||||
chr12:68915781
|
G | A | 6 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+16897C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915781 | ||||||
chr12:68915810
|
G | A | 44 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(41): Show | 44 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.160+16868C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915810 | ||||||
chr12:68915884
|
T | C | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+16794A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915884 | ||||||
chr12:68915940
|
T | C | 13 | a0001c0001t0001g0080a0001c0001t0001g0094a0001c0001t0001g0155others(10): Show | 13 | HG02071.hp2 HG02129.hp1 NA18961.hp1 others(10): Show |
intron_variant | MODIFIER | c.160+16738A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68915940 | ||||||
chr12:68916300
|
T | C | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+16378A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916300 | ||||||
chr12:68916469
|
T | G | 23 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(20): Show | 23 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+16209A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916469 | ||||||
chr12:68916514
|
C | T | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+16164G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916514 | ||||||
chr12:68916598
|
G | C | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+16080C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916598 | ||||||
chr12:68916634
|
T | C | 1 | a0002c0003t0015g0329 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+16044A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916634 | ||||||
chr12:68916639
|
C | T | 2 | a0002c0003t0019g0026a0002c0010t0008g0025 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.160+16039G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916639 | ||||||
chr12:68916720
|
C | T | 3 | a0002c0003t0003g0033a0002c0009t0002g0031a0002c0009t0002g0032 | 3 | HG02809.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160+15958G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916720 | ||||||
chr12:68916752
|
G | A | 161 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0140others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+15926C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916752 | ||||||
chr12:68916781
|
C | T | 2 | a0001c0002t0002g0264a0001c0002t0002g0266 | 2 | HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.160+15897G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916781 | ||||||
chr12:68916829
|
A | G | 6 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+15849T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916829 | ||||||
chr12:68916838
|
G | A | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+15840C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916838 | ||||||
chr12:68916874
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.160+15804G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916874 | ||||||
chr12:68916888
|
C | CA | 10 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0001g0130others(7): Show | 10 | HG00438.hp2 HG00733.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+15789dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916888 | ||||||
chr12:68916888
|
C | CAAAA | 40 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(37): Show | 40 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.160+15786_160+1578 others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916888 | ||||||
chr12:68916888
|
CA | C | 16 | a0001c0001t0001g0166a0001c0001t0001g0230a0001c0001t0004g0229others(13): Show | 16 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+15789delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916888 | ||||||
chr12:68916906
|
A | AG | 6 | a0002c0003t0004g0023a0002c0008t0004g0020a0002c0010t0002g0022others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+15771_160+1577 others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916906 | ||||||
chr12:68916906
|
A | G | 48 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(45): Show | 48 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.160+15772T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916906 | ||||||
chr12:68916956
|
T | C | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+15722A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916956 | ||||||
chr12:68916970
|
T | C | 4 | a0001c0001t0053g0243a0001c0006t0012g0225a0001c0006t0012g0241others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+15708A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68916970 | ||||||
chr12:68917033
|
C | T | 2 | a0001c0001t0003g0059a0001c0004t0011g0058 | 2 | HG03669.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.160+15645G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917033 | ||||||
chr12:68917144
|
A | G | 3 | a0002c0003t0004g0019a0002c0005t0016g0003a0002c0005t0016g0004 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.160+15534T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917144 | ||||||
chr12:68917151
|
A | G | 1 | a0001c0001t0018g0228 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.160+15527T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917151 | ||||||
chr12:68917198
|
G | A | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+15480C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917198 | ||||||
chr12:68917213
|
C | G | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+15465G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917213 | ||||||
chr12:68917225
|
C | CTCT | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+15452_160+1545 others(7): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917225 | ||||||
chr12:68917273
|
C | T | 161 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0140others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+15405G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917273 | ||||||
chr12:68917461
|
G | A | 1 | a0001c0007t0003g0147 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160+15217C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917461 | ||||||
chr12:68917531
|
G | C | 5 | a0001c0001t0004g0203a0001c0006t0008g0226a0001c0006t0008g0244others(2): Show | 5 | HG02257.hp2 HG02615.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+15147C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917531 | ||||||
chr12:68917682
|
G | C | 2 | a0001c0004t0005g0148a0001c0004t0005g0149 | 2 | HG01074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.160+14996C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917682 | ||||||
chr12:68917714
|
T | C | 2 | a0002c0003t0027g0005a0002c0003t0028g0006 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.160+14964A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917714 | ||||||
chr12:68917796
|
C | T | 39 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(36): Show | 39 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.160+14882G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917796 | ||||||
chr12:68917848
|
T | A | 1 | a0001c0001t0066g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+14830A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917848 | ||||||
chr12:68917884
|
C | G | 42 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(39): Show | 42 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.160+14794G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917884 | ||||||
chr12:68917997
|
TTCCTGCA others(5): Show |
T | 3 | a0001c0001t0001g0094a0001c0002t0001g0306a0001c0002t0010g0093 | 3 | NA18961.hp1 NA18991.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.160+14669_160+1468 others(16): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68917997 | ||||||
chr12:68918033
|
C | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0207 | 2 | HG00280.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.160+14645G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918033 | ||||||
chr12:68918105
|
C | A | 41 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(38): Show | 41 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.160+14573G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918105 | ||||||
chr12:68918190
|
C | T | 274 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(271): Show | 275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.160+14488G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918190 | ||||||
chr12:68918196
|
C | T | 3 | a0002c0003t0003g0015a0002c0005t0013g0009a0002c0005t0013g0010 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.160+14482G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918196 | ||||||
chr12:68918330
|
T | C | 1 | a0001c0001t0003g0265 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.160+14348A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918330 | ||||||
chr12:68918396
|
C | A | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+14282G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918396 | ||||||
chr12:68918403
|
G | A | 1 | a0001c0002t0006g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.160+14275C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918403 | ||||||
chr12:68918498
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.160+14180A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918498 | ||||||
chr12:68918530
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.160+14148G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918530 | ||||||
chr12:68918612
|
T | TAATCC | 4 | a0001c0007t0001g0132a0002c0003t0004g0019a0002c0005t0016g0003others(1): Show | 4 | HG01516.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+14061_160+1406 others(9): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918612 | ||||||
chr12:68918612
|
T | TAATCCAA others(3): Show |
40 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(37): Show | 40 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.160+14056_160+1406 others(14): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918612 | ||||||
chr12:68918645
|
C | T | 3 | a0002c0003t0004g0019a0002c0005t0016g0003a0002c0005t0016g0004 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.160+14033G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918645 | ||||||
chr12:68918713
|
A | T | 1 | a0001c0001t0066g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+13965T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918713 | ||||||
chr12:68918743
|
A | C | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+13935T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918743 | ||||||
chr12:68918838
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.160+13840C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68918838 | ||||||
chr12:68919059
|
T | C | 1 | a0002c0003t0028g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160+13619A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919059 | ||||||
chr12:68919149
|
A | G | 20 | a0002c0003t0003g0328a0002c0003t0004g0019a0002c0003t0007g0324others(17): Show | 20 | HG00639.hp1 HG02145.hp1 HG02717.hp2 others(17): Show |
intron_variant | MODIFIER | c.160+13529T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919149 | ||||||
chr12:68919315
|
T | C | 50 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(47): Show | 50 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(47): Show |
intron_variant | MODIFIER | c.160+13363A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919315 | ||||||
chr12:68919636
|
C | T | 1 | a0001c0004t0012g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160+13042G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919636 | ||||||
chr12:68919819
|
G | A | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+12859C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919819 | ||||||
chr12:68919826
|
C | T | 1 | a0002c0003t0015g0330 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.160+12852G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919826 | ||||||
chr12:68919908
|
T | C | 1 | a0001c0001t0010g0136 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.160+12770A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919908 | ||||||
chr12:68919968
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.160+12710G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68919968 | ||||||
chr12:68920036
|
G | A | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+12642C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920036 | ||||||
chr12:68920068
|
C | G | 1 | a0001c0002t0050g0092 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.160+12610G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920068 | ||||||
chr12:68920093
|
G | T | 1 | a0002c0003t0028g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160+12585C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920093 | ||||||
chr12:68920237
|
A | G | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+12441T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920237 | ||||||
chr12:68920472
|
T | C | 3 | a0002c0003t0003g0033a0002c0009t0002g0031a0002c0009t0002g0032 | 3 | HG02809.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160+12206A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920472 | ||||||
chr12:68920624
|
G | C | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+12054C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920624 | ||||||
chr12:68920646
|
G | C | 1 | a0001c0002t0001g0283 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+12032C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920646 | ||||||
chr12:68920671
|
CT | C | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+12006delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920671 | ||||||
chr12:68920693
|
C | CT | 47 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0254others(44): Show | 47 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(44): Show |
intron_variant | MODIFIER | c.160+11984dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920693 | ||||||
chr12:68920698
|
T | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0002t0001g0064others(3): Show | 6 | NA18946.hp1 NA18962.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+11980A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920698 | ||||||
chr12:68920698
|
TC | T | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+11979delG | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920698 | ||||||
chr12:68920699
|
C | T | 243 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(240): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.160+11979G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920699 | ||||||
chr12:68920760
|
G | A | 150 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0140others(147): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.160+11918C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920760 | ||||||
chr12:68920857
|
A | AT | 12 | a0001c0002t0001g0081a0001c0002t0006g0286a0001c0004t0005g0145others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.160+11820dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920857 | ||||||
chr12:68920967
|
G | T | 8 | a0002c0003t0004g0023a0002c0003t0057g0008a0002c0008t0004g0020others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+11711C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68920967 | ||||||
chr12:68921014
|
T | A | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+11664A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921014 | ||||||
chr12:68921055
|
T | TC | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+11622_160+1162 others(5): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921055 | ||||||
chr12:68921123
|
C | T | 1 | a0002c0008t0025g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+11555G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921123 | ||||||
chr12:68921155
|
G | T | 161 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0140others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+11523C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921155 | ||||||
chr12:68921229
|
C | T | 1 | a0002c0005t0002g0323 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+11449G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921229 | ||||||
chr12:68921235
|
G | A | 1 | a0002c0003t0001g0313 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+11443C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921235 | ||||||
chr12:68921296
|
C | G | 161 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0140others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+11382G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921296 | ||||||
chr12:68921341
|
C | T | 150 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0140others(147): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.160+11337G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921341 | ||||||
chr12:68921472
|
T | G | 50 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(47): Show | 50 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(47): Show |
intron_variant | MODIFIER | c.160+11206A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921472 | ||||||
chr12:68921474
|
T | C | 3 | a0002c0005t0002g0309a0002c0005t0002g0310a0002c0005t0002g0323 | 3 | HG02145.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.160+11204A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921474 | ||||||
chr12:68921512
|
T | A | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+11166A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921512 | ||||||
chr12:68921636
|
C | T | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+11042G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921636 | ||||||
chr12:68921862
|
A | G | 43 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(40): Show | 43 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.160+10816T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68921862 | ||||||
chr12:68922084
|
T | C | 249 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(246): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.160+10594A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922084 | ||||||
chr12:68922182
|
T | A | 3 | a0002c0003t0004g0019a0002c0005t0016g0003a0002c0005t0016g0004 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.160+10496A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922182 | ||||||
chr12:68922186
|
C | T | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+10492G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922186 | ||||||
chr12:68922222
|
G | A | 8 | a0002c0003t0004g0023a0002c0003t0057g0008a0002c0008t0004g0020others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+10456C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922222 | ||||||
chr12:68922284
|
T | C | 10 | a0002c0003t0003g0033a0002c0003t0004g0019a0002c0003t0025g0007others(7): Show | 10 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+10394A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922284 | ||||||
chr12:68922522
|
G | C | 1 | a0002c0008t0025g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+10156C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922522 | ||||||
chr12:68922528
|
C | G | 1 | a0001c0007t0003g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.160+10150G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922528 | ||||||
chr12:68922560
|
T | G | 40 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(37): Show | 40 | HG00438.hp1 HG00639.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.160+10118A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922560 | ||||||
chr12:68922567
|
G | A | 9 | a0002c0003t0003g0328a0002c0003t0015g0329a0002c0003t0015g0330others(6): Show | 9 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+10111C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922567 | ||||||
chr12:68922618
|
AT | A | 182 | a0001c0001t0001g0074a0001c0001t0001g0108a0001c0001t0001g0122others(179): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.160+10059delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922618 | ||||||
chr12:68922618
|
ATTT | A | 38 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(35): Show | 38 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.160+10057_160+1005 others(7): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922618 | ||||||
chr12:68922742
|
C | T | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+9936G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68922742 | ||||||
chr12:68923002
|
A | T | 7 | a0002c0003t0003g0033a0002c0003t0025g0007a0002c0003t0027g0005others(4): Show | 7 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+9676T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923002 | ||||||
chr12:68923046
|
A | G | 250 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(247): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+9632T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923046 | ||||||
chr12:68923157
|
TAG | T | 27 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0183others(24): Show | 27 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.160+9519_160+9520d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923157 | ||||||
chr12:68923158
|
A | AGT | 7 | a0001c0001t0001g0173a0001c0002t0001g0174a0001c0002t0054g0175others(4): Show | 7 | HG02080.hp2 HG02809.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+9519_160+9520i others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
A | AGTGT | 3 | a0001c0002t0002g0264a0002c0003t0007g0324a0002c0008t0019g0325 | 3 | HG01993.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.160+9519_160+9520i others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGT | A | 35 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0192others(32): Show | 35 | HG00280.hp2 HG00423.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.160+9516_160+9519d others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGT | A | 52 | a0001c0001t0001g0060a0001c0001t0001g0122a0001c0001t0001g0151others(49): Show | 52 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.160+9514_160+9519d others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(1): Show |
A | 52 | a0001c0001t0001g0072a0001c0001t0001g0160a0001c0001t0001g0161others(49): Show | 53 | HG00140.hp1 HG00544.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.160+9512_160+9519d others(10): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(3): Show |
A | 28 | a0001c0001t0001g0070a0001c0001t0055g0305a0001c0002t0001g0035others(25): Show | 28 | HG00438.hp1 HG00733.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.160+9510_160+9519d others(12): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(5): Show |
A | 13 | a0001c0001t0001g0248a0001c0001t0002g0303a0001c0002t0001g0034others(10): Show | 13 | HG01123.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+9508_160+9519d others(14): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(7): Show |
A | 5 | a0001c0002t0001g0261a0001c0002t0001g0262a0002c0003t0029g0018others(2): Show | 5 | HG00639.hp1 HG02602.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+9506_160+9519d others(16): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(9): Show |
A | 3 | a0002c0010t0046g0029a0003c0011t0012g0028a0004c0013t0004g0027 | 3 | HG02280.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+9504_160+9519d others(18): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(11): Show |
A | 4 | a0002c0003t0004g0023a0002c0003t0057g0008a0002c0009t0044g0021others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9502_160+9519d others(20): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(13): Show |
A | 4 | a0001c0002t0001g0172a0002c0003t0004g0019a0002c0005t0016g0003others(1): Show | 4 | HG00423.hp2 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9500_160+9519d others(22): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923158
|
AGAGTGTG others(25): Show |
A | 4 | a0001c0001t0001g0074a0001c0007t0009g0075a0001c0007t0009g0076others(1): Show | 4 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9488_160+9519d others(34): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923158 | ||||||
chr12:68923160
|
A | AGT | 12 | a0001c0001t0001g0277a0001c0001t0067g0083a0001c0002t0001g0001others(9): Show | 13 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+9516_160+9517d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923160
|
A | AGTGT | 5 | a0001c0001t0001g0080a0001c0001t0002g0121a0001c0002t0001g0079others(2): Show | 5 | HG03927.hp1 HG04199.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9514_160+9517d others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923160
|
A | AGTGTGT | 3 | a0001c0002t0001g0114a0001c0002t0001g0270a0001c0004t0005g0154 | 3 | HG01081.hp1 HG04204.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.160+9512_160+9517d others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923160
|
A | T | 23 | a0001c0001t0001g0053a0001c0001t0001g0140a0001c0001t0001g0173others(20): Show | 23 | HG01109.hp2 HG01516.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+9518T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923160
|
AGT | A | 26 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0098others(23): Show | 26 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+9516_160+9517d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923160
|
AGTGT | A | 10 | a0001c0001t0001g0108a0001c0001t0001g0137a0001c0002t0001g0105others(7): Show | 10 | HG00099.hp2 HG01361.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+9514_160+9517d others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923160
|
AGTGTGT | A | 8 | a0001c0001t0001g0109a0001c0001t0004g0112a0001c0002t0001g0110others(5): Show | 8 | HG01074.hp1 HG02257.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+9512_160+9517d others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923160 | ||||||
chr12:68923204
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0002t0048g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.160+9460_160+9473d others(16): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923204 | ||||||
chr12:68923207
|
GTGTGTGT | G | 3 | a0001c0001t0001g0252a0001c0001t0002g0251a0001c0004t0036g0253 | 3 | HG01516.hp2 NA19062.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.160+9464_160+9470d others(9): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923207 | ||||||
chr12:68923209
|
GTGTGT | G | 3 | a0001c0001t0001g0250a0001c0002t0001g0249a0002c0003t0033g0336 | 3 | HG02922.hp1 NA18944.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.160+9464_160+9468d others(7): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923209 | ||||||
chr12:68923216
|
T | C | 3 | a0001c0001t0003g0265a0001c0002t0002g0264a0001c0002t0002g0266 | 3 | HG01346.hp1 HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.160+9462A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923216 | ||||||
chr12:68923250
|
T | TG | 337 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.160+9427_160+9428i others(3): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923250 | ||||||
chr12:68923510
|
C | T | 2 | a0001c0002t0006g0285a0001c0002t0006g0286 | 2 | HG02258.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.160+9168G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923510 | ||||||
chr12:68923535
|
A | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG00423.hp2 HG02071.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+9143T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923535 | ||||||
chr12:68923843
|
G | A | 1 | a0001c0002t0009g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.160+8835C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923843 | ||||||
chr12:68923915
|
TTAAAACT others(1): Show |
T | 16 | a0002c0003t0003g0328a0002c0003t0007g0324a0002c0003t0015g0329others(13): Show | 16 | HG02145.hp1 HG02717.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+8755_160+8762d others(10): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923915 | ||||||
chr12:68923943
|
A | G | 1 | a0002c0008t0025g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+8735T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923943 | ||||||
chr12:68923952
|
C | T | 274 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(271): Show | 275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.160+8726G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68923952 | ||||||
chr12:68924149
|
T | TA | 58 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(55): Show | 58 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.160+8528dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924149 | ||||||
chr12:68924149
|
TA | T | 23 | a0001c0001t0002g0164a0001c0002t0001g0116a0001c0002t0001g0165others(20): Show | 23 | HG00609.hp2 HG01099.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+8528delT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924149 | ||||||
chr12:68924149
|
TAA | T | 21 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(18): Show | 21 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+8527_160+8528d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924149 | ||||||
chr12:68924222
|
C | T | 1 | a0001c0004t0005g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.160+8456G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924222 | ||||||
chr12:68924347
|
C | T | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+8331G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924347 | ||||||
chr12:68924428
|
C | T | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+8250G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924428 | ||||||
chr12:68924434
|
T | C | 2 | a0001c0002t0001g0261a0001c0002t0001g0262 | 2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.160+8244A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924434 | ||||||
chr12:68924480
|
G | GA | 228 | a0001c0001t0001g0074a0001c0001t0001g0122a0001c0001t0001g0129others(225): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.160+8197dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924480 | ||||||
chr12:68924480
|
G | GAA | 46 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(43): Show | 46 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.160+8196_160+8197d others(4): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924480 | ||||||
chr12:68924695
|
A | G | 1 | a0002c0003t0025g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+7983T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924695 | ||||||
chr12:68924816
|
A | G | 3 | a0002c0003t0004g0019a0002c0005t0016g0003a0002c0005t0016g0004 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.160+7862T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924816 | ||||||
chr12:68924836
|
A | G | 1 | a0002c0005t0023g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.160+7842T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924836 | ||||||
chr12:68924887
|
T | C | 39 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(36): Show | 39 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.160+7791A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924887 | ||||||
chr12:68924950
|
T | C | 2 | a0002c0003t0032g0335a0002c0003t0033g0336 | 2 | HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.160+7728A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68924950 | ||||||
chr12:68925008
|
G | T | 100 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(97): Show | 100 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.160+7670C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925008 | ||||||
chr12:68925019
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.160+7659C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925019 | ||||||
chr12:68925157
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.160+7521C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925157 | ||||||
chr12:68925387
|
C | T | 1 | a0001c0004t0020g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.160+7291G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925387 | ||||||
chr12:68925451
|
A | G | 1 | a0004c0013t0004g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.160+7227T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925451 | ||||||
chr12:68925483
|
G | A | 246 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(243): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.160+7195C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925483 | ||||||
chr12:68925635
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA19066.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.160+7043C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925635 | ||||||
chr12:68925661
|
T | C | 39 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(36): Show | 39 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.160+7017A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925661 | ||||||
chr12:68925788
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.160+6890A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925788 | ||||||
chr12:68925956
|
G | A | 2 | a0001c0002t0001g0068a0001c0002t0001g0071 | 2 | NA18946.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.160+6722C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68925956 | ||||||
chr12:68926328
|
A | G | 1 | a0001c0004t0012g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160+6350T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926328 | ||||||
chr12:68926373
|
A | G | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+6305T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926373 | ||||||
chr12:68926455
|
G | A | 16 | a0002c0003t0003g0328a0002c0003t0007g0324a0002c0003t0015g0329others(13): Show | 16 | HG02145.hp1 HG02717.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+6223C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926455 | ||||||
chr12:68926526
|
C | A | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+6152G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926526 | ||||||
chr12:68926632
|
T | C | 29 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(26): Show | 29 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+6046A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926632 | ||||||
chr12:68926678
|
C | A | 1 | a0002c0003t0029g0018 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+6000G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926678 | ||||||
chr12:68926684
|
G | T | 1 | a0002c0008t0001g0312 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.160+5994C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926684 | ||||||
chr12:68926711
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.160+5967C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926711 | ||||||
chr12:68926717
|
C | G | 4 | a0002c0003t0007g0324a0002c0005t0022g0326a0002c0008t0019g0325others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+5961G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68926717 | ||||||
chr12:68927142
|
G | A | 3 | a0002c0003t0019g0026a0002c0008t0025g0024a0002c0010t0008g0025 | 3 | HG01167.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.160+5536C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927142 | ||||||
chr12:68927182
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.160+5496T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927182 | ||||||
chr12:68927194
|
T | C | 4 | a0001c0001t0001g0263a0001c0001t0003g0265a0001c0002t0002g0264others(1): Show | 4 | HG01071.hp1 HG01346.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+5484A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927194 | ||||||
chr12:68927250
|
G | A | 16 | a0002c0003t0003g0328a0002c0003t0007g0324a0002c0003t0015g0329others(13): Show | 16 | HG02145.hp1 HG02717.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+5428C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927250 | ||||||
chr12:68927303
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.160+5375A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927303 | ||||||
chr12:68927315
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.160+5363A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927315 | ||||||
chr12:68927509
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.160+5169C>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927509 | ||||||
chr12:68927730
|
C | T | 3 | a0002c0003t0003g0033a0002c0009t0002g0031a0002c0009t0002g0032 | 3 | HG02809.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160+4948G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927730 | ||||||
chr12:68927853
|
C | G | 1 | a0002c0003t0003g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+4825G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927853 | ||||||
chr12:68927855
|
C | G | 1 | a0002c0009t0001g0311 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.160+4823G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927855 | ||||||
chr12:68927858
|
T | G | 1 | a0001c0002t0001g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.160+4820A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927858 | ||||||
chr12:68927946
|
C | T | 1 | a0001c0002t0001g0159 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.160+4732G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927946 | ||||||
chr12:68927969
|
C | T | 6 | a0002c0003t0003g0033a0002c0003t0027g0005a0002c0003t0028g0006others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+4709G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927969 | ||||||
chr12:68927984
|
C | T | 98 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(95): Show | 98 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.160+4694G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927984 | ||||||
chr12:68927994
|
T | G | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+4684A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68927994 | ||||||
chr12:68928068
|
T | A | 2 | a0002c0003t0003g0315a0002c0003t0004g0314 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.160+4610A>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928068 | ||||||
chr12:68928109
|
G | A | 30 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(27): Show | 30 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.160+4569C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928109 | ||||||
chr12:68928127
|
G | A | 271 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(268): Show | 272 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.160+4551C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928127 | ||||||
chr12:68928133
|
A | G | 22 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(19): Show | 22 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.160+4545T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928133 | ||||||
chr12:68928181
|
C | A | 1 | a0001c0007t0045g0268 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.160+4497G>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928181 | ||||||
chr12:68928617
|
T | G | 5 | a0001c0002t0003g0146a0001c0004t0005g0145a0001c0004t0005g0148others(2): Show | 5 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+4061A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928617 | ||||||
chr12:68928706
|
A | G | 1 | a0001c0002t0003g0272 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160+3972T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928706 | ||||||
chr12:68928742
|
C | CT | 85 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(82): Show | 85 | HG00438.hp1 HG00544.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.160+3935dupA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928742 | ||||||
chr12:68928911
|
AT | A | 162 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0151others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.160+3766delA | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68928911 | ||||||
chr12:68929011
|
G | C | 9 | a0002c0003t0004g0019a0002c0003t0004g0023a0002c0003t0057g0008others(6): Show | 9 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+3667C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929011 | ||||||
chr12:68929116
|
C | G | 1 | a0002c0003t0030g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+3562G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929116 | ||||||
chr12:68929286
|
C | G | 97 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(94): Show | 97 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+3392G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929286 | ||||||
chr12:68929291
|
T | C | 36 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(33): Show | 36 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.160+3387A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929291 | ||||||
chr12:68929339
|
T | C | 7 | a0002c0003t0007g0317a0002c0003t0007g0320a0002c0003t0007g0322others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+3339A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929339 | ||||||
chr12:68929426
|
A | T | 30 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(27): Show | 30 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.160+3252T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929426 | ||||||
chr12:68929577
|
G | A | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+3101C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929577 | ||||||
chr12:68929789
|
G | A | 97 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(94): Show | 97 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+2889C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929789 | ||||||
chr12:68929914
|
A | T | 4 | a0001c0001t0001g0074a0001c0007t0009g0075a0001c0007t0009g0076others(1): Show | 4 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+2764T>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68929914 | ||||||
chr12:68930168
|
C | T | 1 | a0002c0008t0025g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+2510G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930168 | ||||||
chr12:68930181
|
C | T | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+2497G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930181 | ||||||
chr12:68930192
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.160+2486C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930192 | ||||||
chr12:68930273
|
C | T | 97 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(94): Show | 97 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+2405G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930273 | ||||||
chr12:68930392
|
T | C | 1 | a0001c0001t0055g0305 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160+2286A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930392 | ||||||
chr12:68930448
|
G | C | 1 | a0001c0002t0002g0049 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.160+2230C>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930448 | ||||||
chr12:68930525
|
C | G | 1 | a0001c0002t0001g0073 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.160+2153G>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930525 | ||||||
chr12:68930663
|
T | G | 24 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(21): Show | 24 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.160+2015A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930663 | ||||||
chr12:68930696
|
C | T | 3 | a0002c0005t0002g0309a0002c0005t0002g0310a0002c0005t0002g0323 | 3 | HG02145.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.160+1982G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930696 | ||||||
chr12:68930714
|
A | G | 1 | a0002c0005t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160+1964T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930714 | ||||||
chr12:68930902
|
G | A | 1 | a0001c0002t0001g0271 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.160+1776C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68930902 | ||||||
chr12:68931182
|
C | T | 30 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(27): Show | 30 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.160+1496G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931182 | ||||||
chr12:68931232
|
C | T | 2 | a0002c0005t0016g0003a0002c0005t0016g0004 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+1446G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931232 | ||||||
chr12:68931651
|
A | C | 2 | a0001c0004t0020g0069a0001c0006t0008g0282 | 2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+1027T>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931651 | ||||||
chr12:68931674
|
A | G | 329 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0070others(326): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.160+1004T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931674 | ||||||
chr12:68931693
|
C | CCGAGATC others(1): Show |
6 | a0002c0003t0003g0033a0002c0003t0027g0005a0002c0003t0028g0006others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+977_160+984dup others(8): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931693 | ||||||
chr12:68931702
|
C | T | 45 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(42): Show | 45 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.160+976G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931702 | ||||||
chr12:68931732
|
C | T | 1 | a0002c0003t0025g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+946G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931732 | ||||||
chr12:68931733
|
G | A | 2 | a0001c0001t0001g0281a0001c0002t0062g0280 | 2 | NA18968.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.160+945C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931733 | ||||||
chr12:68931744
|
C | CA | 33 | a0001c0001t0001g0288a0001c0001t0001g0290a0001c0001t0001g0295others(30): Show | 34 | HG00733.hp1 HG01074.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.160+933dupT | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931744 | ||||||
chr12:68931756
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0001g0306 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.160+911_160+921del others(11): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931756 | ||||||
chr12:68931761
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.160+917T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931761 | ||||||
chr12:68931762
|
A | G | 27 | a0001c0002t0001g0037a0001c0002t0001g0039a0001c0002t0001g0040others(24): Show | 27 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+916T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931762 | ||||||
chr12:68931763
|
A | AAAAAAAG others(4): Show |
1 | a0002c0005t0013g0010 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.160+914_160+915ins others(11): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931763 | ||||||
chr12:68931763
|
A | AAAAAAG | 20 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0003g0059others(17): Show | 20 | HG00544.hp2 HG00642.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160+914_160+915ins others(6): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931763 | ||||||
chr12:68931763
|
A | AAAAAAGA others(3): Show |
2 | a0001c0007t0002g0051a0002c0005t0013g0009 | 2 | HG02896.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.160+914_160+915ins others(10): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931763 | ||||||
chr12:68931763
|
A | AAAAAAGA others(15): Show |
1 | a0002c0003t0025g0007 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+914_160+915ins others(22): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931763 | ||||||
chr12:68931763
|
A | AAAAAGAA others(6): Show |
1 | a0002c0003t0057g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.160+914_160+915ins others(13): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931763 | ||||||
chr12:68931763
|
A | G | 1 | a0001c0002t0001g0034 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.160+915T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931763 | ||||||
chr12:68931764
|
AAAG | A | 41 | a0001c0002t0001g0037a0001c0002t0001g0039a0001c0002t0001g0040others(38): Show | 41 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.160+911_160+913del others(3): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931764 | ||||||
chr12:68931764
|
AAAGAAAG | A | 7 | a0002c0003t0003g0033a0002c0003t0027g0005a0002c0003t0030g0030others(4): Show | 7 | HG02451.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+907_160+913del others(7): Show |
CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931764 | ||||||
chr12:68931942
|
A | G | 45 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(42): Show | 45 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.160+736T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68931942 | ||||||
chr12:68932149
|
C | T | 1 | a0001c0002t0031g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.160+529G>A | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68932149 | ||||||
chr12:68932269
|
A | G | 45 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(42): Show | 45 | HG00438.hp1 HG01358.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.160+409T>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 2/8 | chr12 | 68932269 | ||||||
chr12:68932879
|
T | G | 2 | a0001c0002t0001g0307a0001c0002t0001g0308 | 2 | HG02129.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-3-39A>C | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 1/8 | chr12 | 68932879 | ||||||
chr12:68932952
|
T | C | 29 | a0002c0003t0001g0313a0002c0003t0003g0315a0002c0003t0003g0328others(26): Show | 29 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.-3-112A>G | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 1/8 | chr12 | 68932952 | ||||||
chr12:68933135
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG06807.hp2 | splice_region_variant&intron_variant | LOW | c.-4+7C>T | CPM | ENSG00000135678.12 | transcript | ENST00000551568.6 | protein_coding | 1/8 | chr12 | 68933135 |