geneid | 80315 |
---|---|
ensemblid | ENSG00000113742.14 |
hgncid | 21747 |
symbol | CPEB4 |
name | cytoplasmic polyadenylation element binding protein 4 |
refseq_nuc | NM_030627.4 |
refseq_prot | NP_085130.2 |
ensembl_nuc | ENST00000265085.10 |
ensembl_prot | ENSP00000265085.5 |
mane_status | MANE Select |
chr | chr5 |
start | 173888349 |
end | 173961980 |
strand | + |
ver | v1.2 |
region | chr5:173888349-173961980 |
region5000 | chr5:173883349-173966980 |
regionname0 | CPEB4_chr5_173888349_173961980 |
regionname5000 | CPEB4_chr5_173883349_173966980 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 729 | 370 | 86 | 72 | 160 | 10 | 40 | 120 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0002 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0003 | 0/0 | 729 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2190 | 364 | 86 | 69 | 159 | 9 | 39 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0002 | 0/0 | 2190 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0003 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0004 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0005 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0006 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0007 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
c0008 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7229 | 70 | 0 | 17 | 50 | 0 | 3 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0002 | 0/0 | 7227 | 64 | 9 | 8 | 35 | 1 | 11 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0003 | 0/0 | 7228 | 43 | 11 | 8 | 19 | 2 | 3 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0004 | 0/0 | 7235 | 41 | 4 | 12 | 16 | 4 | 5 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0005 | 0/0 | 7228 | 40 | 14 | 9 | 10 | 1 | 6 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0006 | 1/0 | 7229 | 24 | 15 | 5 | 0 | 1 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0007 | 0/1 | 7228 | 17 | 1 | 4 | 9 | 1 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0008 | 0/0 | 7229 | 7 | 7 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0009 | 0/0 | 7223 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0010 | 0/0 | 7228 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0011 | 0/0 | 7228 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0012 | 0/0 | 7230 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0013 | 0/0 | 7229 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0014 | 0/0 | 7227 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0015 | 0/0 | 7228 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0016 | 0/0 | 7229 | 2 | 0 | 1 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0017 | 0/0 | 7229 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0018 | 0/0 | 7227 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0019 | 0/0 | 7228 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0020 | 0/0 | 7229 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0021 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0022 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0023 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0024 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0025 | 0/0 | 7227 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0026 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0027 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0028 | 0/0 | 7227 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0029 | 0/0 | 7227 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0030 | 0/0 | 7229 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0031 | 0/0 | 7229 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0032 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0033 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0034 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0035 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0036 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0037 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0038 | 0/0 | 7227 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0039 | 0/0 | 7177 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0040 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0041 | 0/0 | 7229 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0042 | 0/0 | 7229 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0043 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0044 | 0/0 | 7229 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0045 | 0/0 | 7229 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0046 | 0/0 | 7227 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0047 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0048 | 0/0 | 7228 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0049 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0050 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0051 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0052 | 0/0 | 7228 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0053 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0054 | 0/0 | 7234 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0055 | 0/0 | 7235 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0056 | 0/0 | 7235 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0057 | 0/0 | 7235 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
t0058 | 0/0 | 7235 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2190 | 364 | 86 | 69 | 159 | 9 | 39 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0002 | 0/0 | 2190 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0003 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0004 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0005 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0008 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0002c0006 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0003c0007 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9418 | 70 | 0 | 17 | 50 | 0 | 3 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0002 | 0/0 | 9416 | 63 | 9 | 8 | 35 | 1 | 10 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0003 | 0/0 | 9417 | 42 | 11 | 8 | 19 | 1 | 3 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0004 | 0/0 | 9424 | 39 | 4 | 11 | 15 | 4 | 5 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0005 | 0/0 | 9417 | 39 | 13 | 9 | 10 | 1 | 6 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0006 | 1/0 | 9418 | 23 | 14 | 5 | 0 | 1 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0007 | 0/1 | 9417 | 17 | 1 | 4 | 9 | 1 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0008 | 0/0 | 9418 | 7 | 7 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0009 | 0/0 | 9412 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0010 | 0/0 | 9417 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0011 | 0/0 | 9417 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0012 | 0/0 | 9419 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0013 | 0/0 | 9418 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0014 | 0/0 | 9416 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0015 | 0/0 | 9417 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0016 | 0/0 | 9418 | 2 | 0 | 1 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0017 | 0/0 | 9418 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0019 | 0/0 | 9417 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0020 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0021 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0022 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0023 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0024 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0025 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0026 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0027 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0028 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0029 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0030 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0031 | 0/0 | 9418 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0032 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0033 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0034 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0035 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0036 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0037 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0038 | 0/0 | 9416 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0039 | 0/0 | 9366 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0040 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0041 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0042 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0043 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0044 | 0/0 | 9418 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0045 | 0/0 | 9418 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0046 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0047 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0048 | 0/0 | 9417 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0049 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0050 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0051 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0052 | 0/0 | 9417 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0053 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0054 | 0/0 | 9423 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0055 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0056 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0057 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0001t0058 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0002t0018 | 0/0 | 9416 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0003t0002 | 0/0 | 9416 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0004t0003 | 0/0 | 9417 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0005t0004 | 0/0 | 9424 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0001c0008t0004 | 0/0 | 9424 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0002c0006t0006 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
a0003c0007t0005 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | copy fasta | chr5 | 173883349 | 173966980 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0010g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0012g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0014g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0015g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0015g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0016g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0016g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0017g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0017g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0019g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0019g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0020g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0021g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0022g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0023g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0024g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0025g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0026g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0027g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0028g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0029g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0030g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0031g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0032g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0033g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0034g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0035g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0036g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0037g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0038g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0039g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0040g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0041g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0042g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0043g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0044g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0045g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0046g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0047g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0048g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0049g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0050g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0051g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0052g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0053g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0054g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0055g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0056g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0057g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0001t0058g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0002t0018g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0004t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0005t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0001c0008t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0002c0006t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
a0003c0007t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0292 | EUR | GBR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0280 | EUR | FIN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0101 | EUR | FIN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00408 | hp1 | a0001 | c0001 | t0020 | g0015 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0318 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00544 | hp2 | a0001 | c0001 | t0030 | g0313 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0128 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00735 | hp2 | a0001 | c0001 | t0031 | g0121 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0295 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0191 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01074 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0170 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01099 | hp1 | a0001 | c0001 | t0023 | g0194 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01109 | hp2 | a0001 | c0001 | t0048 | g0006 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01167 | hp1 | a0001 | c0002 | t0018 | g0010 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01167 | hp2 | a0001 | c0001 | t0025 | g0308 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01169 | hp2 | a0001 | c0002 | t0018 | g0010 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0296 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01255 | hp1 | a0001 | c0005 | t0004 | g0297 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0250 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0098 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0115 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01346 | hp1 | a0001 | c0001 | t0054 | g0305 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01433 | hp1 | a0001 | c0001 | t0024 | g0206 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0211 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0175 | EUR | IBS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01517 | hp2 | a0001 | c0004 | t0003 | g0045 | EUR | IBS | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0247 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0044 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0249 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0097 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01943 | hp1 | a0001 | c0001 | t0007 | g0171 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0302 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01952 | hp2 | a0001 | c0001 | t0016 | g0048 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0197 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02015 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0042 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02071 | hp1 | a0001 | c0001 | t0056 | g0273 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02080 | hp2 | a0001 | c0001 | t0040 | g0057 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02135 | hp2 | a0001 | c0001 | t0027 | g0264 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02145 | hp2 | a0001 | c0001 | t0022 | g0310 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02165 | hp2 | a0001 | c0001 | t0055 | g0275 | EAS | CDX | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02257 | hp2 | a0003 | c0007 | t0005 | g0184 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02280 | hp1 | a0001 | c0001 | t0015 | g0307 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | PEL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0092 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02572 | hp2 | a0001 | c0001 | t0026 | g0223 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02602 | hp1 | a0001 | c0001 | t0044 | g0136 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02622 | hp1 | a0001 | c0001 | t0021 | g0189 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02647 | hp1 | a0001 | c0001 | t0032 | g0125 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0198 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0320 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02735 | hp1 | a0001 | c0001 | t0016 | g0067 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0290 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02809 | hp2 | a0001 | c0001 | t0035 | g0156 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0040 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0190 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02970 | hp2 | a0001 | c0001 | t0019 | g0039 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03098 | hp2 | a0001 | c0001 | t0011 | g0043 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0129 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0309 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03195 | hp2 | a0001 | c0001 | t0049 | g0267 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0315 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0179 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03453 | hp1 | a0002 | c0006 | t0006 | g0093 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03453 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03491 | hp2 | a0001 | c0001 | t0014 | g0036 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03492 | hp1 | a0001 | c0001 | t0014 | g0036 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0195 | AFR | GWD | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03669 | hp1 | a0001 | c0001 | t0028 | g0227 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0085 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03704 | hp1 | a0001 | c0001 | t0046 | g0228 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0208 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0205 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03927 | hp2 | a0001 | c0001 | t0017 | g0102 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0306 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0077 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0293 | SAS | BEB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04199 | hp2 | a0001 | c0003 | t0002 | g0252 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0291 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0188 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04228 | hp1 | a0001 | c0001 | t0045 | g0149 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0285 | SAS | STU | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0120 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0196 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18946 | hp1 | a0001 | c0001 | t0038 | g0050 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0319 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18951 | hp1 | a0001 | c0001 | t0029 | g0218 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18952 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18959 | hp2 | a0001 | c0001 | t0057 | g0278 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18970 | hp1 | a0001 | c0001 | t0012 | g0100 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18981 | hp2 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18982 | hp1 | a0001 | c0001 | t0052 | g0053 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18986 | hp1 | a0001 | c0001 | t0051 | g0216 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18987 | hp2 | a0001 | c0001 | t0042 | g0004 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18991 | hp2 | a0001 | c0001 | t0058 | g0300 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18997 | hp2 | a0001 | c0001 | t0041 | g0112 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19001 | hp1 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19007 | hp1 | a0001 | c0001 | t0039 | g0065 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19030 | hp2 | a0001 | c0001 | t0033 | g0041 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19062 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19079 | hp1 | a0001 | c0008 | t0004 | g0287 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19080 | hp1 | a0001 | c0001 | t0047 | g0172 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19082 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19084 | hp2 | a0001 | c0001 | t0036 | g0054 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19086 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19087 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19089 | hp1 | a0001 | c0001 | t0043 | g0144 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19089 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19240 | hp1 | a0001 | c0001 | t0053 | g0146 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | YRI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | ASW | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ASW | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0283 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0007 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0270 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20905 | hp1 | a0001 | c0001 | t0017 | g0103 | SAS | GIH | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | GIH | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0167 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02486 | hp1 | a0001 | c0001 | t0034 | g0070 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG02559 | hp2 | a0001 | c0001 | t0050 | g0006 | AFR | ACB | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG06807 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
HG06807 | hp2 | a0001 | c0001 | t0037 | g0118 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0248 | AFR | USA | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | LWK | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0173 | REF | REF | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0119 | REF | REF | CPEB4_chr5_173883349_173966980 | CPEB4 | chr5 | 173883349 | 173966980 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:173889866
|
A | G | 1 | a0003 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.133A>G | p.Ile45Val | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1518/9418 | 133/2190 | 45/729 | chr5 | 173889866 | ||
chr5:173889868
|
A | G | 1 | a0002 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.135A>G | p.Ile45Met | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1520/9418 | 135/2190 | 45/729 | chr5 | 173889868 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:173889853
|
C | T | 1 | a0001c0008 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.120C>T | p.Ser40Ser | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1505/9418 | 120/2190 | 40/729 | chr5 | 173889853 | ||
chr5:173890015
|
G | A | 1 | a0001c0003 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.282G>A | p.Gln94Gln | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1667/9418 | 282/2190 | 94/729 | chr5 | 173890015 | ||
chr5:173890363
|
C | T | 1 | a0001c0005 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.630C>T | p.Phe210Phe | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 2015/9418 | 630/2190 | 210/729 | chr5 | 173890363 | ||
chr5:173944977
|
A | C | 1 | a0001c0002 | 2 | HG01167.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1293A>C | p.Ser431Ser | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/10 | 2678/9418 | 1293/2190 | 431/729 | chr5 | 173944977 | ||
chr5:173953194
|
G | A | 1 | a0001c0004 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.1884G>A | p.Ala628Ala | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/10 | 3269/9418 | 1884/2190 | 628/729 | chr5 | 173953194 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:173888413
|
T | TGGC | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-1305_-1303dupGGC | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1302 | INFO_REALIGN_3_PRIME | chr5 | 173888413 | ||||
chr5:173888657
|
T | C | 1 | a0001c0001t0020 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1077T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 1077 | chr5 | 173888657 | |||||
chr5:173888771
|
C | T | 1 | a0001c0001t0053 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-963C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 963 | chr5 | 173888771 | |||||
chr5:173888858
|
A | T | 1 | a0001c0001t0052 | 1 | NA18982.hp1 | 5_prime_UTR_variant | MODIFIER | c.-876A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 876 | chr5 | 173888858 | |||||
chr5:173888863
|
C | G | 7 | a0001c0001t0007a0001c0001t0019a0001c0001t0047others(4): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-871C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | chr5 | 173888863 | ||||||
chr5:173888880
|
C | T | 1 | a0001c0001t0046 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-854C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 854 | chr5 | 173888880 | |||||
chr5:173889229
|
A | G | 1 | a0001c0002t0018 | 2 | HG01167.hp1 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-505A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 505 | chr5 | 173889229 | |||||
chr5:173889471
|
A | C | 1 | a0001c0001t0045 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-263A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 263 | chr5 | 173889471 | |||||
chr5:173889501
|
T | C | 1 | a0001c0001t0021 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-233T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | chr5 | 173889501 | ||||||
chr5:173889726
|
G | A | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(33): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
5_prime_UTR_variant | MODIFIER | c.-8G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/10 | 8 | chr5 | 173889726 | |||||
chr5:173956153
|
C | T | 1 | a0001c0001t0058 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 16 | chr5 | 173956153 | |||||
chr5:173956191
|
C | A | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*54C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 54 | chr5 | 173956191 | |||||
chr5:173956498
|
A | G | 1 | a0001c0001t0030 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*361A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 361 | chr5 | 173956498 | |||||
chr5:173956553
|
G | A | 2 | a0001c0001t0022a0001c0001t0031 | 2 | HG00735.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*416G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 416 | chr5 | 173956553 | |||||
chr5:173956603
|
C | CTT | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*481_*482dupTT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 483 | INFO_REALIGN_3_PRIME | chr5 | 173956603 | ||||
chr5:173956605
|
T | A | 10 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(7): Show | 59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*468T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 468 | chr5 | 173956605 | |||||
chr5:173956793
|
C | T | 1 | a0001c0001t0024 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 656 | chr5 | 173956793 | |||||
chr5:173957129
|
C | T | 1 | a0001c0001t0057 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 992 | chr5 | 173957129 | |||||
chr5:173957460
|
A | C | 1 | a0001c0001t0013 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1323A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1323 | chr5 | 173957460 | |||||
chr5:173957539
|
A | G | 1 | a0001c0001t0051 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1402 | chr5 | 173957539 | |||||
chr5:173957559
|
C | T | 1 | a0001c0001t0029 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1422C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1422 | chr5 | 173957559 | |||||
chr5:173957660
|
T | A | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1523T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 1523 | chr5 | 173957660 | |||||
chr5:173958501
|
A | G | 1 | a0001c0001t0050 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2364 | chr5 | 173958501 | |||||
chr5:173958676
|
A | G | 1 | a0001c0001t0028 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2539A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2539 | chr5 | 173958676 | |||||
chr5:173958690
|
T | TA | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2563dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2564 | INFO_REALIGN_3_PRIME | chr5 | 173958690 | ||||
chr5:173958905
|
G | C | 6 | a0001c0001t0007a0001c0001t0047a0001c0001t0048others(3): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2768G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 2768 | chr5 | 173958905 | |||||
chr5:173959150
|
AG | A | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3016delG | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3016 | INFO_REALIGN_3_PRIME | chr5 | 173959150 | ||||
chr5:173959200
|
C | T | 8 | a0001c0001t0001a0001c0001t0012a0001c0001t0020others(5): Show | 79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3063C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3063 | chr5 | 173959200 | |||||
chr5:173959499
|
G | C | 1 | a0001c0001t0047 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3362G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3362 | chr5 | 173959499 | |||||
chr5:173959506
|
A | G | 1 | a0001c0001t0017 | 2 | HG03927.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3369A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3369 | chr5 | 173959506 | |||||
chr5:173959539
|
A | T | 1 | a0001c0001t0056 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3402A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3402 | chr5 | 173959539 | |||||
chr5:173959623
|
T | A | 1 | a0001c0001t0041 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3486T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3486 | chr5 | 173959623 | |||||
chr5:173959625
|
A | T | 1 | a0001c0001t0041 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3488A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3488 | chr5 | 173959625 | |||||
chr5:173959676
|
A | G | 1 | a0001c0001t0044 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3539A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3539 | chr5 | 173959676 | |||||
chr5:173959677
|
T | C | 1 | a0001c0001t0016 | 2 | HG01952.hp2 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3540T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3540 | chr5 | 173959677 | |||||
chr5:173959874
|
T | A | 1 | a0001c0001t0041 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3737T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 3737 | chr5 | 173959874 | |||||
chr5:173960332
|
C | A | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4195C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4195 | chr5 | 173960332 | |||||
chr5:173960467
|
G | A | 1 | a0001c0001t0032 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4330G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4330 | chr5 | 173960467 | |||||
chr5:173960493
|
C | T | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG02071.hp1 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4356C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4356 | chr5 | 173960493 | |||||
chr5:173960506
|
T | C | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*4369T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4369 | chr5 | 173960506 | |||||
chr5:173960528
|
T | G | 2 | a0001c0001t0011a0001c0001t0033 | 4 | HG01891.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4391T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4391 | chr5 | 173960528 | |||||
chr5:173960699
|
T | A | 1 | a0001c0001t0022 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4562T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4562 | chr5 | 173960699 | |||||
chr5:173960791
|
C | T | 1 | a0001c0001t0040 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4654C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4654 | chr5 | 173960791 | |||||
chr5:173960823
|
T | G | 1 | a0001c0001t0034 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4686T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4686 | chr5 | 173960823 | |||||
chr5:173960844
|
G | T | 1 | a0001c0001t0010 | 3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4707G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4707 | chr5 | 173960844 | |||||
chr5:173960852
|
A | G | 1 | a0001c0001t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4715A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4715 | chr5 | 173960852 | |||||
chr5:173960866
|
CTTTGA | C | 1 | a0001c0001t0009 | 3 | HG02965.hp2 HG03540.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4736_*4740delTTGA others(1): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4736 | INFO_REALIGN_3_PRIME | chr5 | 173960866 | ||||
chr5:173960924
|
T | C | 1 | a0001c0001t0035 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4787T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4787 | chr5 | 173960924 | |||||
chr5:173960932
|
A | T | 16 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(13): Show | 127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4795A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4795 | chr5 | 173960932 | |||||
chr5:173960957
|
AGGATTTA others(44): Show |
A | 1 | a0001c0001t0039 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4821_*4871delGGAT others(47): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4821 | chr5 | 173960957 | |||||
chr5:173961047
|
T | C | 1 | a0001c0001t0036 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4910T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4910 | chr5 | 173961047 | |||||
chr5:173961094
|
G | A | 16 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(13): Show | 127 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*4957G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4957 | chr5 | 173961094 | |||||
chr5:173961101
|
T | C | 1 | a0001c0001t0019 | 2 | HG02886.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4964T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 4964 | chr5 | 173961101 | |||||
chr5:173961308
|
G | T | 8 | a0001c0001t0004a0001c0001t0054a0001c0001t0055others(5): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*5171G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5171 | chr5 | 173961308 | |||||
chr5:173961340
|
A | G | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5203A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5203 | chr5 | 173961340 | |||||
chr5:173961441
|
G | A | 1 | a0001c0001t0037 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5304G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5304 | chr5 | 173961441 | |||||
chr5:173961516
|
T | A | 1 | a0001c0001t0026 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5379T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5379 | chr5 | 173961516 | |||||
chr5:173961717
|
AT | A | 28 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(25): Show | 131 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*5595delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5595 | INFO_REALIGN_3_PRIME | chr5 | 173961717 | ||||
chr5:173961717
|
ATT | A | 9 | a0001c0001t0002a0001c0001t0014a0001c0001t0025others(6): Show | 73 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*5594_*5595delTT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5594 | INFO_REALIGN_3_PRIME | chr5 | 173961717 | ||||
chr5:173961752
|
A | T | 10 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(7): Show | 59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*5615A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5615 | chr5 | 173961752 | |||||
chr5:173961864
|
G | A | 1 | a0001c0001t0048 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5727G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5727 | chr5 | 173961864 | |||||
chr5:173961945
|
C | CA | 9 | a0001c0001t0004a0001c0001t0012a0001c0001t0042others(6): Show | 49 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*5817dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 10/10 | 5818 | INFO_REALIGN_3_PRIME | chr5 | 173961945 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:173890981
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1125+123C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173890981 | ||||||
chr5:173891146
|
T | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+288T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891146 | ||||||
chr5:173891147
|
G | GAGAATCA others(81): Show |
13 | a0001c0001t0005g0035a0001c0001t0005g0311a0001c0001t0005g0312others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+370_1125+371i others(90): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173891147 | |||||
chr5:173891249
|
A | T | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+391A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891249 | ||||||
chr5:173891251
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+393A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891251 | ||||||
chr5:173891554
|
G | A | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+696G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891554 | ||||||
chr5:173891916
|
AAAT | A | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+1060_1125+106 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173891916 | |||||
chr5:173891939
|
G | C | 1 | a0001c0001t0013g0037 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1125+1081G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891939 | ||||||
chr5:173891984
|
C | A | 1 | a0001c0001t0005g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1125+1126C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173891984 | ||||||
chr5:173892055
|
T | C | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1125+1197T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892055 | ||||||
chr5:173892102
|
A | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+1244A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892102 | ||||||
chr5:173892260
|
G | A | 4 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0044others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1402G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892260 | ||||||
chr5:173892274
|
A | AT | 15 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(12): Show | 15 | HG01891.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+1431dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | |||||
chr5:173892274
|
A | ATTTTTTT | 28 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(25): Show | 34 | HG00099.hp1 HG00280.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1125+1425_1125+143 others(11): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | |||||
chr5:173892274
|
A | ATTTTTTT others(1): Show |
77 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(74): Show | 86 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1125+1424_1125+143 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | |||||
chr5:173892274
|
A | ATTTTTTT others(2): Show |
50 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(47): Show | 57 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1125+1423_1125+143 others(13): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | |||||
chr5:173892274
|
A | ATTTTTTT others(3): Show |
18 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0253others(15): Show | 20 | HG00639.hp1 HG00673.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1125+1422_1125+143 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | |||||
chr5:173892274
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0002g0268a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG02071.hp2 HG02145.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+1421_1125+143 others(15): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892274 | |||||
chr5:173892674
|
T | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+1816T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892674 | ||||||
chr5:173892848
|
A | G | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+1990A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173892848 | ||||||
chr5:173892997
|
C | CTG | 44 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(41): Show | 54 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1125+2178_1125+217 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTG | 37 | a0001c0001t0001g0023a0001c0001t0001g0150a0001c0001t0001g0151others(34): Show | 40 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1125+2176_1125+217 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTGTG | 11 | a0001c0001t0002g0033a0001c0001t0002g0243a0001c0001t0002g0244others(8): Show | 13 | HG00544.hp2 HG00738.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1125+2174_1125+217 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0005g0317a0001c0001t0005g0318a0001c0001t0005g0319others(2): Show | 6 | HG00423.hp1 HG02683.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+2172_1125+217 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0005g0207a0001c0001t0005g0251a0001c0001t0006g0153 | 3 | HG02257.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1125+2170_1125+217 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0005g0208 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1125+2168_1125+217 others(16): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTGTGT others(7): Show |
1 | a0001c0001t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1125+2166_1125+217 others(18): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0006g0155 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1125+2164_1125+217 others(20): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
CTG | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0080others(54): Show | 66 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1125+2178_1125+217 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
CTGTG | C | 32 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0002g0210others(29): Show | 38 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1125+2176_1125+217 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
CTGTGTG | C | 3 | a0001c0001t0004g0295a0001c0001t0004g0296a0001c0001t0005g0209 | 3 | HG00741.hp1 HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1125+2174_1125+217 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173892997
|
CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0004g0294 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1125+2164_1125+217 others(20): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173892997 | |||||
chr5:173893030
|
TGTGTGTG others(1): Show |
T | 3 | a0001c0001t0019g0039a0001c0001t0019g0040a0001c0001t0049g0267 | 3 | HG02886.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1125+2174_1125+218 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893030 | |||||
chr5:173893032
|
TGTGTGA | T | 16 | a0001c0001t0004g0288a0001c0001t0004g0289a0001c0001t0007g0006others(13): Show | 17 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1125+2176_1125+218 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893032 | |||||
chr5:173893034
|
TGTGA | T | 5 | a0001c0001t0007g0025a0001c0001t0007g0167a0001c0001t0007g0178others(2): Show | 6 | HG02015.hp1 HG02109.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+2178_1125+218 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893034 | |||||
chr5:173893036
|
T | A | 6 | a0001c0001t0001g0049a0001c0001t0004g0269a0001c0001t0005g0177others(3): Show | 6 | HG01952.hp2 HG02486.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1125+2178T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893036 | ||||||
chr5:173893036
|
T | TGA | 10 | a0001c0001t0001g0002a0001c0001t0001g0083a0001c0001t0001g0084others(7): Show | 14 | HG00438.hp1 HG00544.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.1125+2196_1125+219 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | |||||
chr5:173893036
|
T | TGTGTGA | 6 | a0001c0001t0001g0145a0001c0001t0005g0186a0001c0001t0005g0188others(3): Show | 7 | HG00558.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | |||||
chr5:173893036
|
T | TGTGTGTG others(1): Show |
4 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0191others(1): Show | 7 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(12): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | |||||
chr5:173893036
|
T | TGTGTGTG others(3): Show |
13 | a0001c0001t0005g0192a0001c0001t0005g0193a0001c0001t0005g0197others(10): Show | 15 | HG00558.hp2 HG01099.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | |||||
chr5:173893036
|
T | TGTGTGTG others(5): Show |
10 | a0001c0001t0005g0038a0001c0001t0005g0199a0001c0001t0005g0200others(7): Show | 10 | HG01243.hp1 HG01255.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1125+2179_1125+218 others(16): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | |||||
chr5:173893036
|
TGA | T | 7 | a0001c0001t0002g0221a0001c0001t0006g0122a0001c0001t0006g0123others(4): Show | 7 | HG01167.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+2196_1125+219 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893036 | |||||
chr5:173893038
|
A | T | 2 | a0001c0001t0002g0259a0001c0001t0003g0166 | 2 | HG02723.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1125+2180A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893038 | ||||||
chr5:173893152
|
C | A | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1125+2294C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893152 | ||||||
chr5:173893203
|
T | C | 1 | a0001c0001t0004g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1125+2345T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893203 | ||||||
chr5:173893223
|
A | G | 2 | a0001c0001t0006g0120a0001c0001t0031g0121 | 2 | HG00735.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1125+2365A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893223 | ||||||
chr5:173893424
|
T | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(321): Show | 370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.1125+2566T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893424 | ||||||
chr5:173893442
|
C | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1125+2584C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893442 | ||||||
chr5:173893456
|
A | G | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1125+2598A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893456 | ||||||
chr5:173893573
|
GA | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(64): Show | 80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1125+2724delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173893573 | |||||
chr5:173893696
|
C | T | 3 | a0001c0001t0005g0177a0001c0001t0021g0189a0003c0007t0005g0184 | 3 | HG02257.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1125+2838C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893696 | ||||||
chr5:173893812
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+2954G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173893812 | ||||||
chr5:173894193
|
C | T | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+3335C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894193 | ||||||
chr5:173894259
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1125+3401G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894259 | ||||||
chr5:173894295
|
T | G | 1 | a0001c0001t0006g0128 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1125+3437T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894295 | ||||||
chr5:173894336
|
T | A | 1 | a0001c0001t0038g0050 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1125+3478T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894336 | ||||||
chr5:173894342
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1125+3484G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894342 | ||||||
chr5:173894395
|
C | T | 1 | a0001c0001t0019g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1125+3537C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894395 | ||||||
chr5:173894412
|
A | G | 1 | a0001c0008t0004g0287 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1125+3554A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894412 | ||||||
chr5:173894491
|
G | A | 1 | a0001c0001t0030g0313 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1125+3633G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894491 | ||||||
chr5:173894620
|
C | CA | 55 | a0001c0001t0004g0290a0001c0001t0005g0007a0001c0001t0005g0027others(52): Show | 64 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1125+3781dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173894620 | |||||
chr5:173894620
|
CA | C | 59 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(56): Show | 67 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1125+3781delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173894620 | |||||
chr5:173894841
|
C | A | 1 | a0001c0001t0004g0295 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1125+3983C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894841 | ||||||
chr5:173894925
|
G | A | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+4067G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173894925 | ||||||
chr5:173895209
|
T | C | 60 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(57): Show | 68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1125+4351T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895209 | ||||||
chr5:173895239
|
A | T | 1 | a0001c0001t0004g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1125+4381A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895239 | ||||||
chr5:173895402
|
A | G | 1 | a0001c0001t0006g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1125+4544A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895402 | ||||||
chr5:173895531
|
G | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(321): Show | 370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.1125+4673G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895531 | ||||||
chr5:173895616
|
T | C | 1 | a0001c0001t0006g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1125+4758T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895616 | ||||||
chr5:173895816
|
G | A | 1 | a0001c0001t0015g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1125+4958G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895816 | ||||||
chr5:173895835
|
C | G | 1 | a0001c0001t0003g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1125+4977C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895835 | ||||||
chr5:173895836
|
T | G | 1 | a0001c0001t0005g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1125+4978T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173895836 | ||||||
chr5:173896166
|
C | T | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+5308C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896166 | ||||||
chr5:173896199
|
C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1125+5341C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896199 | ||||||
chr5:173896653
|
T | C | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1125+5795T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896653 | ||||||
chr5:173896834
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1125+5976C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173896834 | ||||||
chr5:173897113
|
T | C | 13 | a0001c0001t0005g0035a0001c0001t0005g0311a0001c0001t0005g0312others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1125+6255T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897113 | ||||||
chr5:173897426
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1125+6568T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897426 | ||||||
chr5:173897574
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1125+6716G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897574 | ||||||
chr5:173897620
|
A | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+6762A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897620 | ||||||
chr5:173897711
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1125+6853C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897711 | ||||||
chr5:173897804
|
G | T | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1125+6946G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897804 | ||||||
chr5:173897869
|
A | G | 1 | a0001c0001t0003g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1125+7011A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897869 | ||||||
chr5:173897877
|
CAT | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+7020_1125+702 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897877 | ||||||
chr5:173897905
|
A | G | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+7047A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897905 | ||||||
chr5:173897968
|
G | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+7110G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173897968 | ||||||
chr5:173898591
|
G | A | 1 | a0002c0006t0006g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1125+7733G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898591 | ||||||
chr5:173898651
|
G | A | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1125+7793G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898651 | ||||||
chr5:173898715
|
T | C | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+7857T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898715 | ||||||
chr5:173898740
|
G | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1125+7882G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898740 | ||||||
chr5:173898834
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1125+7976G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173898834 | ||||||
chr5:173899123
|
C | T | 1 | a0001c0001t0002g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1125+8265C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899123 | ||||||
chr5:173899196
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1125+8338C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899196 | ||||||
chr5:173899577
|
C | T | 113 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(110): Show | 130 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1125+8719C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899577 | ||||||
chr5:173899711
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+8853A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899711 | ||||||
chr5:173899738
|
T | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+8880T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899738 | ||||||
chr5:173899863
|
A | G | 1 | a0001c0001t0004g0293 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1125+9005A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899863 | ||||||
chr5:173899888
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+9030C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173899888 | ||||||
chr5:173900023
|
C | G | 60 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(57): Show | 68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1125+9165C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900023 | ||||||
chr5:173900143
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1125+9285C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900143 | ||||||
chr5:173900195
|
C | A | 18 | a0001c0001t0005g0038a0001c0001t0005g0186a0001c0001t0005g0192others(15): Show | 20 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1125+9337C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900195 | ||||||
chr5:173900386
|
C | T | 1 | a0001c0001t0003g0014 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1125+9528C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900386 | ||||||
chr5:173900405
|
C | CA | 20 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(17): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1125+9560dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173900405 | |||||
chr5:173900490
|
A | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+9632A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900490 | ||||||
chr5:173900538
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1125+9680C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900538 | ||||||
chr5:173900637
|
T | C | 1 | a0001c0005t0004g0297 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1125+9779T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900637 | ||||||
chr5:173900686
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1125+9828T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900686 | ||||||
chr5:173900790
|
T | C | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1126-9733T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900790 | ||||||
chr5:173900889
|
C | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0266 | 2 | HG00639.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1126-9634C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900889 | ||||||
chr5:173900933
|
C | T | 6 | a0001c0001t0003g0013a0001c0001t0003g0071a0001c0001t0003g0072others(3): Show | 7 | HG00438.hp2 HG00621.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-9590C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173900933 | ||||||
chr5:173901017
|
G | T | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-9506G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901017 | ||||||
chr5:173901021
|
G | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-9502G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901021 | ||||||
chr5:173901202
|
T | C | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-9321T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901202 | ||||||
chr5:173901240
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1126-9283T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901240 | ||||||
chr5:173901279
|
A | G | 4 | a0001c0001t0005g0007a0001c0001t0005g0188a0001c0001t0005g0191others(1): Show | 6 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-9244A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901279 | ||||||
chr5:173901298
|
A | G | 3 | a0001c0001t0004g0034a0001c0001t0004g0285a0001c0001t0004g0291 | 4 | HG01256.hp1 HG01258.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-9225A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901298 | ||||||
chr5:173901329
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1126-9194A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901329 | ||||||
chr5:173901518
|
C | T | 2 | a0001c0001t0005g0320a0001c0001t0014g0036 | 3 | HG02683.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1126-9005C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901518 | ||||||
chr5:173901615
|
C | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-8908C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901615 | ||||||
chr5:173901617
|
G | T | 21 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1126-8906G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901617 | ||||||
chr5:173901814
|
C | G | 34 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0038others(31): Show | 40 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1126-8709C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901814 | ||||||
chr5:173901834
|
A | G | 1 | a0001c0001t0003g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1126-8689A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901834 | ||||||
chr5:173901958
|
A | G | 1 | a0001c0001t0004g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1126-8565A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173901958 | ||||||
chr5:173902282
|
T | C | 33 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(30): Show | 38 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1126-8241T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902282 | ||||||
chr5:173902633
|
T | C | 6 | a0001c0001t0003g0166a0001c0001t0011g0042a0001c0001t0011g0043others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-7890T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902633 | ||||||
chr5:173902668
|
C | T | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1126-7855C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902668 | ||||||
chr5:173902749
|
G | C | 1 | a0001c0001t0003g0051 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1126-7774G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902749 | ||||||
chr5:173902850
|
C | T | 2 | a0001c0001t0004g0291a0001c0001t0032g0125 | 2 | HG02647.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1126-7673C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902850 | ||||||
chr5:173902886
|
T | C | 1 | a0001c0001t0006g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1126-7637T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902886 | ||||||
chr5:173902952
|
T | G | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1126-7571T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173902952 | ||||||
chr5:173903060
|
G | GA | 5 | a0001c0001t0001g0106a0001c0001t0001g0135a0001c0001t0045g0149others(2): Show | 6 | HG01167.hp1 HG01169.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1126-7447dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173903060 | |||||
chr5:173903060
|
GA | G | 49 | a0001c0001t0001g0143a0001c0001t0001g0163a0001c0001t0002g0240others(46): Show | 55 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1126-7447delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173903060 | |||||
chr5:173903082
|
A | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-7441A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903082 | ||||||
chr5:173903461
|
C | T | 1 | a0001c0001t0021g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1126-7062C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903461 | ||||||
chr5:173903517
|
A | C | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1126-7006A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903517 | ||||||
chr5:173903540
|
T | G | 2 | a0001c0001t0006g0097a0001c0001t0006g0098 | 2 | HG01256.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1126-6983T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173903540 | ||||||
chr5:173903862
|
GA | G | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126-6658delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173903862 | |||||
chr5:173904271
|
G | A | 33 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(30): Show | 38 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1126-6252G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904271 | ||||||
chr5:173904590
|
A | G | 44 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(41): Show | 51 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1126-5933A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904590 | ||||||
chr5:173904655
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1126-5868T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904655 | ||||||
chr5:173904678
|
A | C | 1 | a0001c0001t0003g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1126-5845A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904678 | ||||||
chr5:173904690
|
A | T | 113 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(110): Show | 129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1126-5833A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904690 | ||||||
chr5:173904727
|
T | TC | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(260): Show | 301 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.1126-5795dupC | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904727 | |||||
chr5:173904848
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-5675A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904848 | ||||||
chr5:173904962
|
C | A | 1 | a0001c0001t0005g0317 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1126-5561C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173904962 | ||||||
chr5:173904972
|
G | GATA | 27 | a0001c0001t0002g0217a0001c0001t0002g0222a0001c0001t0003g0011others(24): Show | 30 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1126-5507_1126-550 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | |||||
chr5:173904972
|
G | GATAATA | 4 | a0001c0001t0003g0075a0001c0001t0006g0123a0001c0001t0006g0124others(1): Show | 4 | HG02647.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-5510_1126-550 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | |||||
chr5:173904972
|
GATA | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(60): Show | 75 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1126-5507_1126-550 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | |||||
chr5:173904972
|
GATAATA | G | 12 | a0001c0001t0001g0126a0001c0001t0001g0150a0001c0001t0001g0164others(9): Show | 16 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1126-5510_1126-550 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173904972 | |||||
chr5:173905001
|
TAATAATA others(11): Show |
T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-5519_1126-550 others(22): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905001 | |||||
chr5:173905004
|
TAATAATA others(8): Show |
T | 2 | a0001c0001t0002g0253a0001c0002t0018g0010 | 3 | HG01167.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1126-5516_1126-550 others(19): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905004 | |||||
chr5:173905007
|
TAATAATA others(5): Show |
T | 9 | a0001c0001t0002g0029a0001c0001t0002g0213a0001c0001t0005g0251others(6): Show | 11 | HG01167.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1126-5513_1126-550 others(16): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905007 | |||||
chr5:173905010
|
TAATAATA others(2): Show |
T | 25 | a0001c0001t0002g0030a0001c0001t0002g0180a0001c0001t0002g0225others(22): Show | 28 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1126-5510_1126-550 others(13): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905010 | |||||
chr5:173905013
|
TAATAAA | T | 69 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0032others(66): Show | 78 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1126-5507_1126-550 others(10): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905013 | |||||
chr5:173905014
|
A | G | 4 | a0001c0001t0005g0209a0001c0001t0009g0190a0001c0001t0009g0195others(1): Show | 4 | HG02965.hp2 HG03516.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-5509A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905014 | ||||||
chr5:173905016
|
T | A | 2 | a0001c0001t0006g0128a0002c0006t0006g0093 | 2 | HG00733.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1126-5507T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905016 | ||||||
chr5:173905016
|
TAAA | T | 59 | a0001c0001t0002g0239a0001c0001t0002g0244a0001c0001t0002g0246others(56): Show | 66 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1126-5502_1126-550 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173905016 | |||||
chr5:173905019
|
A | T | 12 | a0001c0001t0001g0160a0001c0001t0002g0217a0001c0001t0002g0220others(9): Show | 13 | HG00741.hp1 HG01175.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1126-5504A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905019 | ||||||
chr5:173905374
|
C | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-5149C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905374 | ||||||
chr5:173905608
|
T | C | 1 | a0001c0001t0005g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1126-4915T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905608 | ||||||
chr5:173905639
|
C | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-4884C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905639 | ||||||
chr5:173905726
|
G | A | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1126-4797G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905726 | ||||||
chr5:173905763
|
G | T | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-4760G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173905763 | ||||||
chr5:173906343
|
T | C | 1 | a0001c0001t0005g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1126-4180T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906343 | ||||||
chr5:173906583
|
C | T | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1126-3940C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906583 | ||||||
chr5:173906719
|
T | C | 1 | a0001c0001t0002g0231 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1126-3804T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906719 | ||||||
chr5:173906847
|
C | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-3676C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906847 | ||||||
chr5:173906872
|
A | T | 2 | a0001c0001t0016g0048a0001c0001t0016g0067 | 2 | HG01952.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1126-3651A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906872 | ||||||
chr5:173906906
|
C | T | 18 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0167others(15): Show | 19 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1126-3617C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173906906 | ||||||
chr5:173907025
|
T | C | 26 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(23): Show | 28 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1126-3498T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907025 | ||||||
chr5:173907127
|
C | T | 7 | a0001c0001t0005g0038a0001c0001t0005g0192a0001c0001t0005g0200others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1126-3396C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907127 | ||||||
chr5:173907181
|
C | T | 21 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1126-3342C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907181 | ||||||
chr5:173907216
|
T | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-3307T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907216 | ||||||
chr5:173907267
|
A | AAAC | 8 | a0001c0001t0004g0283a0001c0001t0004g0290a0001c0001t0005g0316others(5): Show | 9 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1126-3229_1126-322 others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173907267 | |||||
chr5:173907302
|
G | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-3221G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907302 | ||||||
chr5:173907380
|
A | C | 2 | a0001c0001t0005g0198a0001c0001t0005g0205 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1126-3143A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907380 | ||||||
chr5:173907393
|
C | T | 5 | a0001c0001t0005g0311a0001c0001t0005g0316a0001c0001t0005g0317others(2): Show | 5 | HG00423.hp1 HG00558.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-3130C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907393 | ||||||
chr5:173907398
|
C | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(64): Show | 80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1126-3125C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907398 | ||||||
chr5:173907473
|
A | C | 1 | a0001c0001t0002g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1126-3050A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907473 | ||||||
chr5:173907498
|
C | T | 1 | a0001c0001t0005g0312 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1126-3025C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907498 | ||||||
chr5:173907514
|
A | G | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1126-3009A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907514 | ||||||
chr5:173907535
|
C | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-2988C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907535 | ||||||
chr5:173907576
|
T | C | 113 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(110): Show | 129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1126-2947T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907576 | ||||||
chr5:173907789
|
G | A | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(136): Show | 158 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.1126-2734G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173907789 | ||||||
chr5:173908283
|
T | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-2240T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908283 | ||||||
chr5:173908299
|
A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1126-2224A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908299 | ||||||
chr5:173908379
|
G | A | 1 | a0001c0001t0004g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1126-2144G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908379 | ||||||
chr5:173908601
|
T | C | 1 | a0001c0001t0002g0210 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1126-1922T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908601 | ||||||
chr5:173908654
|
A | G | 3 | a0001c0001t0003g0013a0001c0001t0003g0072a0001c0001t0003g0074 | 4 | HG00621.hp2 HG02155.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-1869A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908654 | ||||||
chr5:173908728
|
G | A | 1 | a0001c0001t0007g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1126-1795G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908728 | ||||||
chr5:173908737
|
G | C | 1 | a0001c0001t0004g0295 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1126-1786G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173908737 | ||||||
chr5:173908823
|
TTGTAA | T | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1126-1694_1126-169 others(9): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173908823 | |||||
chr5:173908920
|
CTT | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1126-1601_1126-160 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173908920 | |||||
chr5:173909157
|
A | G | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1126-1366A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909157 | ||||||
chr5:173909243
|
T | G | 1 | a0001c0001t0006g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1126-1280T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909243 | ||||||
chr5:173909341
|
G | C | 2 | a0001c0001t0015g0307a0001c0001t0025g0308 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1126-1182G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909341 | ||||||
chr5:173909528
|
G | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1126-995G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909528 | ||||||
chr5:173909531
|
AT | A | 305 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(302): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1126-980delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173909531 | |||||
chr5:173909682
|
T | C | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1126-841T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909682 | ||||||
chr5:173909788
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1126-735C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909788 | ||||||
chr5:173909789
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-734G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909789 | ||||||
chr5:173909846
|
G | A | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1126-677G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909846 | ||||||
chr5:173909856
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1126-667C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909856 | ||||||
chr5:173909925
|
G | A | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126-598G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909925 | ||||||
chr5:173909943
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1126-580T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173909943 | ||||||
chr5:173910130
|
T | C | 1 | a0001c0001t0002g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1126-393T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910130 | ||||||
chr5:173910132
|
C | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0051 | 3 | HG01099.hp2 HG01106.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1126-391C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910132 | ||||||
chr5:173910168
|
A | G | 1 | a0001c0001t0003g0060 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1126-355A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910168 | ||||||
chr5:173910177
|
A | G | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1126-346A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910177 | ||||||
chr5:173910178
|
C | T | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1126-345C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910178 | ||||||
chr5:173910208
|
A | AT | 8 | a0001c0001t0003g0166a0001c0001t0011g0042a0001c0001t0011g0043others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126-303dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 173910208 | |||||
chr5:173910228
|
T | C | 1 | a0001c0001t0007g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1126-295T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910228 | ||||||
chr5:173910292
|
G | T | 1 | a0001c0001t0005g0251 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1126-231G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910292 | ||||||
chr5:173910373
|
G | A | 1 | a0001c0001t0023g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1126-150G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 1/9 | chr5 | 173910373 | ||||||
chr5:173910621
|
A | C | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1207+17A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910621 | ||||||
chr5:173910720
|
T | G | 2 | a0001c0001t0003g0052a0001c0001t0003g0061 | 2 | NA18959.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1207+116T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910720 | ||||||
chr5:173910850
|
T | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+246T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910850 | ||||||
chr5:173910855
|
A | G | 1 | a0001c0001t0004g0306 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1207+251A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173910855 | ||||||
chr5:173910882
|
A | AT | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0131others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+286dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173910882 | |||||
chr5:173911024
|
G | A | 3 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0032g0125 | 3 | HG02647.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1207+420G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911024 | ||||||
chr5:173911081
|
T | TA | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+486dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911081 | |||||
chr5:173911141
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0213 | 3 | NA18943.hp1 NA19058.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1207+537C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911141 | ||||||
chr5:173911184
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0031g0121 | 2 | HG00735.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1207+580C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911184 | ||||||
chr5:173911196
|
G | T | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1207+592G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911196 | ||||||
chr5:173911207
|
C | A | 1 | a0001c0001t0044g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1207+603C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911207 | ||||||
chr5:173911263
|
G | A | 1 | a0001c0001t0006g0115 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207+659G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911263 | ||||||
chr5:173911273
|
G | GT | 25 | a0001c0001t0002g0238a0001c0001t0007g0006a0001c0001t0007g0024others(22): Show | 27 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1207+674dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911273 | |||||
chr5:173911279
|
A | T | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1207+675A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911279 | ||||||
chr5:173911309
|
C | T | 1 | a0001c0001t0051g0216 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1207+705C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911309 | ||||||
chr5:173911386
|
C | T | 1 | a0001c0001t0021g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1207+782C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911386 | ||||||
chr5:173911397
|
G | A | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+793G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911397 | ||||||
chr5:173911523
|
A | G | 1 | a0001c0001t0006g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1207+919A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911523 | ||||||
chr5:173911609
|
C | T | 2 | a0001c0001t0004g0295a0001c0001t0004g0296 | 2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1207+1005C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911609 | ||||||
chr5:173911681
|
G | GT | 11 | a0001c0001t0003g0064a0001c0001t0003g0132a0001c0001t0004g0272others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207+1100dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | |||||
chr5:173911681
|
G | GTT | 35 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(32): Show | 41 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1207+1099_1207+110 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | |||||
chr5:173911681
|
GT | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(177): Show | 208 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1207+1100delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | |||||
chr5:173911681
|
GTT | G | 28 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0002g0008others(25): Show | 32 | HG01943.hp1 HG02071.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.1207+1099_1207+110 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911681 | |||||
chr5:173911758
|
CTTCA | C | 6 | a0001c0001t0003g0154a0001c0001t0005g0198a0001c0001t0005g0205others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207+1183_1207+118 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173911758 | |||||
chr5:173911870
|
G | C | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1207+1266G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911870 | ||||||
chr5:173911912
|
T | C | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0131others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+1308T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173911912 | ||||||
chr5:173912022
|
G | A | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1207+1418G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912022 | ||||||
chr5:173912041
|
AT | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1207+1438delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912041 | ||||||
chr5:173912058
|
G | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0187 | 3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1207+1454G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912058 | ||||||
chr5:173912132
|
T | C | 1 | a0001c0001t0004g0291 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1207+1528T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912132 | ||||||
chr5:173912219
|
G | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+1615G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912219 | ||||||
chr5:173912367
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1207+1763A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912367 | ||||||
chr5:173912528
|
T | C | 44 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(41): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1207+1924T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912528 | ||||||
chr5:173912626
|
A | AT | 17 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0003g0058others(14): Show | 20 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1207+2038dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173912626 | |||||
chr5:173912626
|
AT | A | 21 | a0001c0001t0001g0016a0001c0001t0001g0090a0001c0001t0001g0137others(18): Show | 22 | HG00280.hp2 HG00609.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1207+2038delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173912626 | |||||
chr5:173912642
|
T | A | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2038T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912642 | ||||||
chr5:173912643
|
A | T | 1 | a0001c0001t0002g0237 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1207+2039A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912643 | ||||||
chr5:173912647
|
A | T | 1 | a0001c0001t0006g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207+2043A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912647 | ||||||
chr5:173912779
|
A | T | 1 | a0002c0006t0006g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1207+2175A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912779 | ||||||
chr5:173912839
|
C | A | 60 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(57): Show | 68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1207+2235C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912839 | ||||||
chr5:173912852
|
A | G | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1207+2248A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912852 | ||||||
chr5:173912882
|
C | T | 1 | a0001c0001t0006g0101 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1207+2278C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912882 | ||||||
chr5:173912883
|
A | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(64): Show | 80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1207+2279A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912883 | ||||||
chr5:173912910
|
C | T | 1 | a0002c0006t0006g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1207+2306C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173912910 | ||||||
chr5:173912918
|
C | CA | 115 | a0001c0001t0001g0083a0001c0001t0001g0109a0001c0001t0001g0116others(112): Show | 131 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1207+2334dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173912918 | |||||
chr5:173913355
|
G | A | 41 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(38): Show | 48 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1207+2751G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913355 | ||||||
chr5:173913493
|
T | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+2889T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913493 | ||||||
chr5:173913914
|
G | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+3310G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913914 | ||||||
chr5:173913949
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1207+3345A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173913949 | ||||||
chr5:173914421
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1207+3817A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173914421 | ||||||
chr5:173914613
|
G | A | 1 | a0001c0001t0056g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1207+4009G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173914613 | ||||||
chr5:173914656
|
T | C | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1207+4052T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173914656 | ||||||
chr5:173915146
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1207+4542C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915146 | ||||||
chr5:173915174
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1207+4570G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915174 | ||||||
chr5:173915463
|
A | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+4859A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915463 | ||||||
chr5:173915487
|
C | T | 1 | a0001c0001t0005g0320 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1207+4883C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915487 | ||||||
chr5:173915542
|
C | A | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1207+4938C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915542 | ||||||
chr5:173915747
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1207+5143A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915747 | ||||||
chr5:173915749
|
G | A | 1 | a0001c0001t0009g0195 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1207+5145G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915749 | ||||||
chr5:173915755
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1207+5151T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915755 | ||||||
chr5:173915994
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1207+5390C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173915994 | ||||||
chr5:173916099
|
A | C | 1 | a0001c0001t0004g0281 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1207+5495A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916099 | ||||||
chr5:173916230
|
G | C | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+5626G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916230 | ||||||
chr5:173916274
|
A | G | 3 | a0001c0001t0004g0269a0001c0001t0004g0280a0001c0005t0004g0297 | 3 | HG00280.hp1 HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1207+5670A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916274 | ||||||
chr5:173916296
|
A | G | 1 | a0001c0001t0006g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1207+5692A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916296 | ||||||
chr5:173916513
|
G | A | 1 | a0001c0001t0005g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207+5909G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916513 | ||||||
chr5:173916617
|
C | T | 1 | a0001c0001t0006g0124 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207+6013C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916617 | ||||||
chr5:173916632
|
G | C | 1 | a0001c0001t0003g0074 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1207+6028G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916632 | ||||||
chr5:173916852
|
A | G | 2 | a0001c0001t0006g0129a0001c0001t0006g0133 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1207+6248A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916852 | ||||||
chr5:173916897
|
G | C | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1207+6293G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173916897 | ||||||
chr5:173917101
|
G | A | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1207+6497G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917101 | ||||||
chr5:173917150
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+6546T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917150 | ||||||
chr5:173917158
|
A | G | 1 | a0001c0001t0031g0121 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1207+6554A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917158 | ||||||
chr5:173917175
|
A | G | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+6571A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917175 | ||||||
chr5:173917658
|
G | A | 1 | a0001c0001t0005g0197 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1207+7054G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917658 | ||||||
chr5:173917874
|
C | G | 1 | a0002c0006t0006g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1207+7270C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917874 | ||||||
chr5:173917891
|
G | C | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1207+7287G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173917891 | ||||||
chr5:173918020
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+7416A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918020 | ||||||
chr5:173918083
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1207+7479A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918083 | ||||||
chr5:173918223
|
C | CTGTA | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1207+7620_1207+762 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173918223 | |||||
chr5:173918349
|
C | T | 3 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0025g0308 | 3 | HG01167.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1207+7745C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918349 | ||||||
chr5:173918406
|
G | T | 33 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0013others(30): Show | 38 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1207+7802G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918406 | ||||||
chr5:173918484
|
T | C | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+7880T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918484 | ||||||
chr5:173918909
|
A | T | 1 | a0001c0001t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1207+8305A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918909 | ||||||
chr5:173918963
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1207+8359G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173918963 | ||||||
chr5:173919082
|
C | T | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1207+8478C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919082 | ||||||
chr5:173919552
|
C | G | 1 | a0001c0001t0035g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1207+8948C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919552 | ||||||
chr5:173919575
|
A | G | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+8971A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919575 | ||||||
chr5:173919582
|
G | C | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+8978G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919582 | ||||||
chr5:173919617
|
G | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1207+9013G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919617 | ||||||
chr5:173919623
|
G | A | 1 | a0001c0001t0005g0316 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207+9019G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919623 | ||||||
chr5:173919648
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(305): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1207+9044T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919648 | ||||||
chr5:173919805
|
C | G | 21 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1207+9201C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919805 | ||||||
chr5:173919830
|
T | C | 3 | a0001c0001t0003g0076a0001c0001t0003g0094a0001c0001t0036g0054 | 3 | HG02602.hp2 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1207+9226T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919830 | ||||||
chr5:173919949
|
G | C | 1 | a0001c0001t0003g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1207+9345G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173919949 | ||||||
chr5:173920072
|
G | A | 3 | a0001c0001t0005g0035a0001c0001t0005g0312a0001c0001t0005g0321 | 4 | NA18947.hp2 NA18956.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+9468G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920072 | ||||||
chr5:173920303
|
T | G | 3 | a0001c0001t0003g0019a0001c0001t0003g0147a0001c0001t0006g0148 | 4 | HG02109.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+9699T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920303 | ||||||
chr5:173920350
|
G | C | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+9746G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920350 | ||||||
chr5:173920385
|
A | G | 1 | a0001c0001t0002g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1207+9781A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920385 | ||||||
chr5:173920565
|
G | T | 1 | a0001c0001t0003g0079 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1207+9961G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920565 | ||||||
chr5:173920817
|
T | C | 1 | a0001c0001t0006g0115 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207+10213T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920817 | ||||||
chr5:173920868
|
C | T | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1207+10264C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920868 | ||||||
chr5:173920890
|
C | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+10286C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173920890 | ||||||
chr5:173921153
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1207+10549G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921153 | ||||||
chr5:173921328
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207+10724G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921328 | ||||||
chr5:173921454
|
G | A | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1207+10850G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921454 | ||||||
chr5:173921476
|
C | G | 2 | a0001c0001t0004g0288a0001c0001t0004g0289 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1207+10872C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921476 | ||||||
chr5:173921599
|
G | C | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1208-10851G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921599 | ||||||
chr5:173921969
|
T | C | 3 | a0001c0001t0004g0271a0001c0001t0004g0274a0001c0001t0004g0282 | 3 | NA18973.hp2 NA19075.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1208-10481T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173921969 | ||||||
chr5:173922042
|
A | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-10408A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922042 | ||||||
chr5:173922113
|
A | G | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1208-10337A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922113 | ||||||
chr5:173922181
|
C | T | 3 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0025g0308 | 3 | HG01167.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-10269C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922181 | ||||||
chr5:173922286
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1208-10164A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922286 | ||||||
chr5:173922333
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1208-10117C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922333 | ||||||
chr5:173922401
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-10049C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922401 | ||||||
chr5:173922649
|
T | A | 2 | a0001c0001t0006g0097a0001c0001t0006g0098 | 2 | HG01256.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1208-9801T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922649 | ||||||
chr5:173922754
|
A | G | 51 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(48): Show | 59 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1208-9696A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922754 | ||||||
chr5:173922788
|
G | A | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1208-9662G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922788 | ||||||
chr5:173922826
|
C | T | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-9624C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922826 | ||||||
chr5:173922837
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-9613A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173922837 | ||||||
chr5:173923402
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-9048A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923402 | ||||||
chr5:173923556
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1208-8894T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923556 | ||||||
chr5:173923562
|
C | A | 1 | a0001c0001t0002g0237 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1208-8888C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923562 | ||||||
chr5:173923813
|
C | T | 1 | a0001c0001t0003g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1208-8637C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923813 | ||||||
chr5:173923814
|
T | A | 1 | a0001c0001t0003g0095 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1208-8636T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923814 | ||||||
chr5:173923987
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-8463G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173923987 | ||||||
chr5:173924078
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-8372C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924078 | ||||||
chr5:173924357
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1208-8093C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924357 | ||||||
chr5:173924485
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-7965C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924485 | ||||||
chr5:173924756
|
C | A | 1 | a0001c0001t0044g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1208-7694C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924756 | ||||||
chr5:173924855
|
G | A | 157 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(154): Show | 180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1208-7595G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924855 | ||||||
chr5:173924858
|
G | T | 157 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(154): Show | 180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1208-7592G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924858 | ||||||
chr5:173924910
|
A | G | 1 | a0001c0001t0006g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1208-7540A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173924910 | ||||||
chr5:173925308
|
T | C | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-7142T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925308 | ||||||
chr5:173925350
|
C | A | 51 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0035others(48): Show | 59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1208-7100C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925350 | ||||||
chr5:173925474
|
G | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0109 | 3 | HG00735.hp1 HG01261.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1208-6976G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925474 | ||||||
chr5:173925712
|
G | A | 1 | a0001c0001t0035g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1208-6738G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925712 | ||||||
chr5:173925760
|
G | A | 308 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(305): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1208-6690G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925760 | ||||||
chr5:173925800
|
T | C | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1208-6650T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173925800 | ||||||
chr5:173926429
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1208-6021T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926429 | ||||||
chr5:173926511
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-5939T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926511 | ||||||
chr5:173926826
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1208-5624G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926826 | ||||||
chr5:173926946
|
C | T | 51 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0035others(48): Show | 59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1208-5504C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173926946 | ||||||
chr5:173927007
|
C | T | 3 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0032g0125 | 3 | HG02647.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1208-5443C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927007 | ||||||
chr5:173927010
|
G | A | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1208-5440G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927010 | ||||||
chr5:173927019
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1208-5431C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927019 | ||||||
chr5:173927044
|
G | A | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1208-5406G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927044 | ||||||
chr5:173927157
|
T | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-5293T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927157 | ||||||
chr5:173927278
|
G | C | 4 | a0001c0001t0006g0012a0001c0001t0006g0068a0001c0001t0006g0069others(1): Show | 5 | HG02486.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-5172G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927278 | ||||||
chr5:173927283
|
T | C | 20 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(17): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1208-5167T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927283 | ||||||
chr5:173927339
|
C | G | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-5111C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927339 | ||||||
chr5:173927370
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1208-5080C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927370 | ||||||
chr5:173927427
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-5023G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927427 | ||||||
chr5:173927543
|
C | T | 1 | a0001c0001t0034g0070 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1208-4907C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927543 | ||||||
chr5:173927620
|
T | C | 1 | a0001c0001t0013g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1208-4830T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927620 | ||||||
chr5:173927650
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1208-4800G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927650 | ||||||
chr5:173927669
|
C | T | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1208-4781C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927669 | ||||||
chr5:173927731
|
C | T | 20 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(17): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1208-4719C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927731 | ||||||
chr5:173927740
|
GCACTC | G | 20 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(17): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1208-4707_1208-470 others(9): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173927740 | |||||
chr5:173927839
|
G | A | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1208-4611G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927839 | ||||||
chr5:173927907
|
A | G | 1 | a0001c0001t0007g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1208-4543A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927907 | ||||||
chr5:173927988
|
A | T | 1 | a0001c0001t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-4462A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173927988 | ||||||
chr5:173928139
|
C | T | 1 | a0001c0001t0007g0212 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1208-4311C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928139 | ||||||
chr5:173928387
|
A | G | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1208-4063A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928387 | ||||||
chr5:173928474
|
C | T | 1 | a0001c0001t0006g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1208-3976C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928474 | ||||||
chr5:173928585
|
G | A | 3 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0025g0308 | 3 | HG01167.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-3865G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928585 | ||||||
chr5:173928711
|
C | T | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1208-3739C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173928711 | ||||||
chr5:173929285
|
A | G | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1208-3165A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929285 | ||||||
chr5:173929288
|
T | A | 3 | a0001c0001t0012g0004a0001c0001t0012g0100a0001c0001t0042g0004 | 4 | NA18952.hp2 NA18970.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-3162T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929288 | ||||||
chr5:173929434
|
C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1208-3016C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929434 | ||||||
chr5:173929538
|
T | A | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1208-2912T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929538 | ||||||
chr5:173929557
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-2893G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929557 | ||||||
chr5:173929614
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1208-2836C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929614 | ||||||
chr5:173929635
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-2815G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929635 | ||||||
chr5:173929658
|
A | G | 1 | a0001c0001t0002g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1208-2792A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929658 | ||||||
chr5:173929745
|
A | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(41): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1208-2705A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929745 | ||||||
chr5:173929749
|
G | C | 44 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(41): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1208-2701G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929749 | ||||||
chr5:173929785
|
G | A | 1 | a0001c0001t0044g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1208-2665G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929785 | ||||||
chr5:173929801
|
A | T | 1 | a0001c0001t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1208-2649A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929801 | ||||||
chr5:173929826
|
A | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0140others(1): Show | 6 | HG01192.hp1 HG01243.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-2624A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173929826 | ||||||
chr5:173930039
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1208-2411C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930039 | ||||||
chr5:173930056
|
G | GT | 8 | a0001c0001t0002g0217a0001c0001t0003g0157a0001c0001t0004g0285others(5): Show | 8 | HG02040.hp1 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-2379dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173930056 | |||||
chr5:173930121
|
C | A | 2 | a0001c0001t0004g0288a0001c0001t0004g0289 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1208-2329C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930121 | ||||||
chr5:173930200
|
A | C | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1208-2250A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930200 | ||||||
chr5:173930203
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-2247G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930203 | ||||||
chr5:173930327
|
G | A | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1208-2123G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930327 | ||||||
chr5:173930392
|
GCTCGTAG others(3): Show |
G | 8 | a0001c0001t0004g0271a0001c0001t0004g0274a0001c0001t0004g0282others(5): Show | 8 | HG02071.hp1 HG02155.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-2054_1208-204 others(14): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173930392 | |||||
chr5:173930403
|
C | G | 51 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(48): Show | 59 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1208-2047C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930403 | ||||||
chr5:173930533
|
C | T | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1208-1917C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930533 | ||||||
chr5:173930671
|
C | A | 1 | a0001c0001t0004g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1208-1779C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930671 | ||||||
chr5:173930715
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1208-1735G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930715 | ||||||
chr5:173930791
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1208-1659A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930791 | ||||||
chr5:173930807
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208-1643T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930807 | ||||||
chr5:173930829
|
A | G | 1 | a0001c0001t0029g0218 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1208-1621A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173930829 | ||||||
chr5:173930990
|
CA | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(285): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1208-1440delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 173930990 | |||||
chr5:173931132
|
A | T | 5 | a0001c0001t0005g0007a0001c0001t0005g0188a0001c0001t0005g0191others(2): Show | 7 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-1318A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931132 | ||||||
chr5:173931151
|
G | A | 132 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(129): Show | 150 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.1208-1299G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931151 | ||||||
chr5:173931288
|
G | A | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1208-1162G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931288 | ||||||
chr5:173931334
|
C | T | 42 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(39): Show | 48 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1208-1116C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931334 | ||||||
chr5:173931954
|
A | G | 31 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0038others(28): Show | 37 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1208-496A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931954 | ||||||
chr5:173931962
|
T | C | 1 | a0001c0001t0002g0221 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1208-488T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173931962 | ||||||
chr5:173932048
|
A | C | 51 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0035others(48): Show | 59 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1208-402A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932048 | ||||||
chr5:173932081
|
G | A | 2 | a0001c0001t0011g0044a0001c0001t0033g0041 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1208-369G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932081 | ||||||
chr5:173932149
|
A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1208-301A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932149 | ||||||
chr5:173932328
|
A | G | 4 | a0001c0001t0002g0030a0001c0001t0002g0230a0001c0001t0002g0260others(1): Show | 5 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-122A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932328 | ||||||
chr5:173932373
|
A | G | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 5 | HG02040.hp2 NA18949.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-77A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 2/9 | chr5 | 173932373 | ||||||
chr5:173932678
|
T | G | 1 | a0001c0001t0005g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1258+178T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173932678 | ||||||
chr5:173932722
|
A | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1258+222A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173932722 | ||||||
chr5:173932998
|
C | T | 98 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(95): Show | 112 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1258+498C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173932998 | ||||||
chr5:173933282
|
G | A | 2 | a0001c0001t0007g0171a0001c0001t0007g0173 | 2 | HG01943.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1258+782G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933282 | ||||||
chr5:173933519
|
A | G | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+1019A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933519 | ||||||
chr5:173933663
|
G | C | 1 | a0001c0001t0005g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1258+1163G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933663 | ||||||
chr5:173933898
|
C | G | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1258+1398C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933898 | ||||||
chr5:173933992
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1258+1492C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933992 | ||||||
chr5:173933993
|
G | A | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1258+1493G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173933993 | ||||||
chr5:173934537
|
C | T | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1258+2037C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934537 | ||||||
chr5:173934545
|
G | A | 1 | a0001c0001t0006g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1258+2045G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934545 | ||||||
chr5:173934699
|
C | A | 1 | a0001c0001t0036g0054 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1258+2199C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934699 | ||||||
chr5:173934707
|
G | A | 1 | a0001c0001t0008g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1258+2207G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934707 | ||||||
chr5:173934777
|
G | A | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1258+2277G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934777 | ||||||
chr5:173934826
|
A | C | 1 | a0001c0001t0006g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1258+2326A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934826 | ||||||
chr5:173934948
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1258+2448C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173934948 | ||||||
chr5:173935106
|
C | T | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+2606C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935106 | ||||||
chr5:173935274
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1258+2774C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935274 | ||||||
chr5:173935309
|
T | C | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0131others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258+2809T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935309 | ||||||
chr5:173935454
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(304): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1258+2954T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935454 | ||||||
chr5:173935455
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1258+2955G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935455 | ||||||
chr5:173935598
|
A | G | 13 | a0001c0001t0005g0035a0001c0001t0005g0311a0001c0001t0005g0312others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1258+3098A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935598 | ||||||
chr5:173935723
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1258+3223C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935723 | ||||||
chr5:173935743
|
C | T | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1258+3243C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173935743 | ||||||
chr5:173935780
|
G | GA | 325 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(322): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1258+3286dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173935780 | |||||
chr5:173936463
|
A | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0160a0001c0001t0001g0165 | 3 | HG01934.hp1 NA18943.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1258+3963A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936463 | ||||||
chr5:173936664
|
G | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(136): Show | 158 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.1258+4164G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936664 | ||||||
chr5:173936771
|
A | G | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1258+4271A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936771 | ||||||
chr5:173936814
|
C | A | 1 | a0001c0001t0001g0081 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1258+4314C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936814 | ||||||
chr5:173936814
|
CT | C | 120 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(117): Show | 136 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1258+4329delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173936814 | |||||
chr5:173936848
|
C | T | 5 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1258+4348C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936848 | ||||||
chr5:173936886
|
C | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(136): Show | 158 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.1258+4386C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936886 | ||||||
chr5:173936907
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1258+4407T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936907 | ||||||
chr5:173936922
|
G | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(304): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1258+4422G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936922 | ||||||
chr5:173936953
|
T | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0260 | 3 | HG01070.hp1 HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1258+4453T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936953 | ||||||
chr5:173936974
|
T | C | 1 | a0001c0001t0004g0276 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1258+4474T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173936974 | ||||||
chr5:173937019
|
C | CT | 9 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0089others(6): Show | 9 | HG01192.hp1 HG02293.hp1 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258+4541dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173937019 | |||||
chr5:173937019
|
CT | C | 45 | a0001c0001t0001g0084a0001c0001t0002g0263a0001c0001t0003g0056others(42): Show | 51 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1258+4541delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173937019 | |||||
chr5:173937019
|
CTT | C | 135 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(132): Show | 154 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1258+4540_1258+454 others(6): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173937019 | |||||
chr5:173937021
|
T | C | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1258+4521T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937021 | ||||||
chr5:173937022
|
T | C | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1258+4522T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937022 | ||||||
chr5:173937090
|
T | C | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1258+4590T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937090 | ||||||
chr5:173937284
|
C | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0187 | 3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1258+4784C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937284 | ||||||
chr5:173937400
|
G | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1258+4900G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937400 | ||||||
chr5:173937874
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1259-5152T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173937874 | ||||||
chr5:173938076
|
A | G | 1 | a0001c0001t0003g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1259-4950A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938076 | ||||||
chr5:173938145
|
A | G | 5 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1259-4881A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938145 | ||||||
chr5:173938273
|
T | C | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1259-4753T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938273 | ||||||
chr5:173938290
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1259-4736A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938290 | ||||||
chr5:173938307
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1259-4719T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938307 | ||||||
chr5:173938423
|
A | G | 1 | a0001c0001t0045g0149 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1259-4603A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938423 | ||||||
chr5:173938445
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1259-4581C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938445 | ||||||
chr5:173938484
|
C | T | 1 | a0001c0001t0052g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1259-4542C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938484 | ||||||
chr5:173938500
|
A | G | 1 | a0001c0001t0004g0276 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1259-4526A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938500 | ||||||
chr5:173938501
|
T | TA | 17 | a0001c0001t0003g0003a0001c0001t0003g0052a0001c0001t0003g0055others(14): Show | 19 | HG01069.hp1 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1259-4524dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173938501 | |||||
chr5:173938534
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1259-4492C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938534 | ||||||
chr5:173938574
|
C | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | NA18949.hp2 NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1259-4452C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938574 | ||||||
chr5:173938712
|
C | T | 1 | a0001c0001t0017g0103 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1259-4314C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938712 | ||||||
chr5:173938757
|
G | A | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1259-4269G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938757 | ||||||
chr5:173938853
|
C | T | 1 | a0001c0001t0006g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1259-4173C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938853 | ||||||
chr5:173938858
|
A | G | 1 | a0001c0001t0006g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1259-4168A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938858 | ||||||
chr5:173938861
|
A | ATATAATA others(9): Show |
1 | a0001c0001t0006g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1259-4165_1259-416 others(20): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173938861 | ||||||
chr5:173939103
|
A | T | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1259-3923A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939103 | ||||||
chr5:173939308
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1259-3718T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939308 | ||||||
chr5:173939341
|
GTACA | G | 277 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(274): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1259-3656_1259-365 others(8): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173939341 | |||||
chr5:173939527
|
C | T | 1 | a0001c0001t0002g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1259-3499C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939527 | ||||||
chr5:173939607
|
A | G | 5 | a0001c0001t0005g0007a0001c0001t0005g0188a0001c0001t0005g0191others(2): Show | 7 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259-3419A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939607 | ||||||
chr5:173939618
|
C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1259-3408C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939618 | ||||||
chr5:173939671
|
C | T | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1259-3355C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939671 | ||||||
chr5:173939742
|
A | G | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0131others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1259-3284A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939742 | ||||||
chr5:173939753
|
CT | C | 135 | a0001c0001t0001g0111a0001c0001t0001g0160a0001c0001t0002g0008others(132): Show | 154 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1259-3260delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173939753 | |||||
chr5:173939890
|
T | C | 7 | a0001c0001t0003g0166a0001c0001t0004g0276a0001c0001t0011g0042others(4): Show | 7 | HG01891.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1259-3136T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939890 | ||||||
chr5:173939956
|
C | CA | 58 | a0001c0001t0001g0078a0001c0001t0002g0008a0001c0001t0002g0009others(55): Show | 66 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1259-3053dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173939956 | |||||
chr5:173939988
|
T | C | 1 | a0001c0001t0003g0058 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1259-3038T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173939988 | ||||||
chr5:173940340
|
T | C | 1 | a0001c0001t0004g0292 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1259-2686T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940340 | ||||||
chr5:173940366
|
T | C | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1259-2660T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940366 | ||||||
chr5:173940391
|
A | T | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1259-2635A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940391 | ||||||
chr5:173940484
|
T | C | 1 | a0001c0001t0004g0296 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1259-2542T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940484 | ||||||
chr5:173940532
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1259-2494T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940532 | ||||||
chr5:173940578
|
G | C | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1259-2448G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940578 | ||||||
chr5:173940583
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1259-2443T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940583 | ||||||
chr5:173940971
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1259-2055C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173940971 | ||||||
chr5:173941137
|
A | G | 1 | a0001c0001t0006g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1259-1889A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941137 | ||||||
chr5:173941177
|
G | C | 3 | a0001c0001t0004g0034a0001c0001t0004g0285a0001c0001t0004g0291 | 4 | HG01256.hp1 HG01258.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259-1849G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941177 | ||||||
chr5:173941548
|
T | A | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1259-1478T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941548 | ||||||
chr5:173941651
|
T | TC | 20 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(17): Show | 22 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1259-1374dupC | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 173941651 | |||||
chr5:173941672
|
A | C | 10 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0188others(7): Show | 13 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1259-1354A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941672 | ||||||
chr5:173941785
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1259-1241C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941785 | ||||||
chr5:173941786
|
G | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0263 | 2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1259-1240G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941786 | ||||||
chr5:173941810
|
G | A | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259-1216G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941810 | ||||||
chr5:173941817
|
G | A | 42 | a0001c0001t0002g0185a0001c0001t0003g0003a0001c0001t0003g0011others(39): Show | 49 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1259-1209G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941817 | ||||||
chr5:173941827
|
G | A | 1 | a0001c0001t0016g0048 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1259-1199G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941827 | ||||||
chr5:173941916
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1259-1110C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941916 | ||||||
chr5:173941989
|
G | C | 1 | a0001c0001t0015g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1259-1037G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941989 | ||||||
chr5:173941997
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1259-1029C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173941997 | ||||||
chr5:173942552
|
T | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(67): Show | 83 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1259-474T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942552 | ||||||
chr5:173942558
|
T | C | 1 | a0001c0001t0004g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1259-468T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942558 | ||||||
chr5:173942642
|
A | G | 1 | a0001c0001t0007g0178 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1259-384A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942642 | ||||||
chr5:173942663
|
A | G | 4 | a0001c0001t0011g0042a0001c0001t0011g0043a0001c0001t0011g0044others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259-363A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942663 | ||||||
chr5:173942970
|
T | C | 1 | a0001c0005t0004g0297 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1259-56T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 3/9 | chr5 | 173942970 | ||||||
chr5:173943312
|
C | T | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1282+263C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943312 | ||||||
chr5:173943485
|
A | G | 33 | a0001c0001t0005g0007a0001c0001t0005g0027a0001c0001t0005g0038others(30): Show | 39 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1282+436A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943485 | ||||||
chr5:173943489
|
A | G | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1282+440A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943489 | ||||||
chr5:173943660
|
T | C | 1 | a0001c0001t0003g0055 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1282+611T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943660 | ||||||
chr5:173943786
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(73): Show | 89 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282+737T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173943786 | ||||||
chr5:173944474
|
C | CA | 7 | a0001c0001t0001g0107a0001c0001t0003g0061a0001c0001t0003g0154others(4): Show | 7 | HG00735.hp2 HG01943.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1283-473dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 173944474 | |||||
chr5:173944474
|
CA | C | 137 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(134): Show | 156 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.1283-473delA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 173944474 | |||||
chr5:173944474
|
CAA | C | 40 | a0001c0001t0002g0181a0001c0001t0004g0001a0001c0001t0004g0034others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1283-474_1283-473d others(4): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 173944474 | |||||
chr5:173944500
|
T | A | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1283-467T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944500 | ||||||
chr5:173944663
|
C | A | 3 | a0001c0001t0005g0177a0001c0001t0021g0189a0003c0007t0005g0184 | 3 | HG02257.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1283-304C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944663 | ||||||
chr5:173944914
|
T | C | 1 | a0001c0001t0015g0309 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1283-53T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944914 | ||||||
chr5:173944938
|
T | G | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1283-29T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944938 | ||||||
chr5:173944941
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1283-26C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 4/9 | chr5 | 173944941 | ||||||
chr5:173945155
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1456+15G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945155 | ||||||
chr5:173945181
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1456+41G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945181 | ||||||
chr5:173945424
|
C | G | 2 | a0001c0001t0004g0288a0001c0001t0004g0289 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1456+284C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945424 | ||||||
chr5:173945480
|
C | CT | 41 | a0001c0001t0001g0080a0001c0001t0004g0001a0001c0001t0004g0034others(38): Show | 47 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1456+345dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 173945480 | |||||
chr5:173945484
|
T | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0060 | 2 | HG01123.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1456+344T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945484 | ||||||
chr5:173945622
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+482G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945622 | ||||||
chr5:173945647
|
T | C | 1 | a0001c0001t0040g0057 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1456+507T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173945647 | ||||||
chr5:173946100
|
G | T | 4 | a0001c0001t0006g0012a0001c0001t0006g0068a0001c0001t0006g0069others(1): Show | 5 | HG02486.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1456+960G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946100 | ||||||
chr5:173946140
|
T | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+1000T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946140 | ||||||
chr5:173946329
|
A | G | 113 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(110): Show | 129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1456+1189A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946329 | ||||||
chr5:173946485
|
A | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+1345A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946485 | ||||||
chr5:173946582
|
G | A | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1456+1442G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946582 | ||||||
chr5:173946887
|
G | A | 4 | a0001c0001t0004g0277a0001c0001t0004g0298a0001c0001t0004g0299others(1): Show | 4 | HG00423.hp2 NA18941.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1456+1747G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946887 | ||||||
chr5:173946945
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1456+1805A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946945 | ||||||
chr5:173946965
|
C | A | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1456+1825C>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173946965 | ||||||
chr5:173947033
|
A | G | 21 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(18): Show | 23 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1456+1893A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947033 | ||||||
chr5:173947155
|
T | G | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1456+2015T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947155 | ||||||
chr5:173947164
|
C | CT | 3 | a0001c0001t0005g0177a0001c0001t0021g0189a0003c0007t0005g0184 | 3 | HG02257.hp2 HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1456+2027dupT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 173947164 | |||||
chr5:173947259
|
G | A | 2 | a0001c0001t0004g0283a0001c0001t0004g0290 | 2 | HG02738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1456+2119G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947259 | ||||||
chr5:173947267
|
G | A | 2 | a0001c0001t0004g0283a0001c0001t0004g0290 | 2 | HG02738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1456+2127G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947267 | ||||||
chr5:173947434
|
C | T | 1 | a0001c0001t0004g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1457-2074C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947434 | ||||||
chr5:173947435
|
G | A | 1 | a0001c0001t0004g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1457-2073G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947435 | ||||||
chr5:173947458
|
C | T | 113 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(110): Show | 129 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1457-2050C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947458 | ||||||
chr5:173947494
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0099a0001c0001t0001g0161 | 3 | NA18978.hp1 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1457-2014A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947494 | ||||||
chr5:173947612
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1457-1896A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947612 | ||||||
chr5:173947652
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1457-1856A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947652 | ||||||
chr5:173947749
|
T | C | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1457-1759T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947749 | ||||||
chr5:173947751
|
T | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(71): Show | 87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1457-1757T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947751 | ||||||
chr5:173947757
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1457-1751C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947757 | ||||||
chr5:173947906
|
G | A | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1457-1602G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947906 | ||||||
chr5:173947952
|
G | A | 112 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(109): Show | 128 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1457-1556G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947952 | ||||||
chr5:173947983
|
C | T | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1457-1525C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173947983 | ||||||
chr5:173948129
|
A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1457-1379A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948129 | ||||||
chr5:173948144
|
A | G | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1457-1364A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948144 | ||||||
chr5:173948153
|
A | C | 1 | a0001c0001t0003g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1457-1355A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948153 | ||||||
chr5:173948165
|
T | A | 22 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(19): Show | 24 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1457-1343T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948165 | ||||||
chr5:173948254
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1457-1254A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948254 | ||||||
chr5:173948419
|
C | T | 3 | a0001c0001t0005g0192a0001c0001t0005g0201a0001c0001t0005g0202 | 3 | HG01884.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1457-1089C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948419 | ||||||
chr5:173948574
|
G | A | 13 | a0001c0001t0005g0035a0001c0001t0005g0311a0001c0001t0005g0312others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1457-934G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948574 | ||||||
chr5:173948670
|
G | C | 60 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(57): Show | 68 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1457-838G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948670 | ||||||
chr5:173948981
|
G | A | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1457-527G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173948981 | ||||||
chr5:173949084
|
A | C | 1 | a0001c0001t0006g0098 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1457-424A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173949084 | ||||||
chr5:173949192
|
C | T | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1457-316C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173949192 | ||||||
chr5:173949503
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
splice_region_variant&intron_variant | LOW | c.1457-5A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 5/9 | chr5 | 173949503 | ||||||
chr5:173949694
|
A | G | 1 | a0001c0001t0002g0255 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1546+97A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 6/9 | chr5 | 173949694 | ||||||
chr5:173949738
|
A | G | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0131others(3): Show | 8 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546+141A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 6/9 | chr5 | 173949738 | ||||||
chr5:173950332
|
T | C | 2 | a0001c0001t0010g0026a0001c0001t0010g0187 | 3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1665+254T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950332 | ||||||
chr5:173950432
|
C | T | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1665+354C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950432 | ||||||
chr5:173950466
|
A | G | 176 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(173): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1665+388A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950466 | ||||||
chr5:173950603
|
C | CAAAAT | 13 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0083others(10): Show | 17 | HG00544.hp1 HG00639.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1665+555_1665+559d others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 173950603 | |||||
chr5:173950603
|
CAAAAT | C | 140 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(137): Show | 159 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.1665+555_1665+559d others(7): Show |
CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 173950603 | |||||
chr5:173950614
|
A | T | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1665+536A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950614 | ||||||
chr5:173950633
|
T | A | 39 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(36): Show | 45 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1665+555T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950633 | ||||||
chr5:173950814
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1665+736G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950814 | ||||||
chr5:173950993
|
G | A | 18 | a0001c0001t0005g0038a0001c0001t0005g0186a0001c0001t0005g0192others(15): Show | 20 | HG01099.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1666-831G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173950993 | ||||||
chr5:173951177
|
A | G | 44 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(41): Show | 50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1666-647A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951177 | ||||||
chr5:173951281
|
C | T | 1 | a0001c0001t0049g0267 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1666-543C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951281 | ||||||
chr5:173951283
|
T | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1666-541T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951283 | ||||||
chr5:173951313
|
T | TA | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1666-502dupA | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 173951313 | |||||
chr5:173951314
|
A | T | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1666-510A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951314 | ||||||
chr5:173951768
|
T | C | 4 | a0001c0001t0004g0277a0001c0001t0004g0298a0001c0001t0004g0299others(1): Show | 4 | HG00423.hp2 NA18941.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1666-56T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951768 | ||||||
chr5:173951812
|
T | C | 1 | a0001c0001t0022g0310 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1666-12T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 7/9 | chr5 | 173951812 | ||||||
chr5:173952103
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1780+165G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952103 | ||||||
chr5:173952344
|
G | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1780+406G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952344 | ||||||
chr5:173952538
|
G | A | 2 | a0001c0001t0019g0039a0001c0001t0019g0040 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1781-553G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952538 | ||||||
chr5:173952643
|
C | G | 1 | a0001c0001t0006g0129 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1781-448C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952643 | ||||||
chr5:173952692
|
A | C | 1 | a0001c0001t0026g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1781-399A>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952692 | ||||||
chr5:173952713
|
A | G | 1 | a0001c0001t0037g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1781-378A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952713 | ||||||
chr5:173952794
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1781-297C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 8/9 | chr5 | 173952794 | ||||||
chr5:173953343
|
C | T | 157 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(154): Show | 180 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1962+71C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953343 | ||||||
chr5:173953344
|
G | A | 1 | a0001c0001t0003g0003 | 3 | HG01069.hp1 HG01074.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1962+72G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953344 | ||||||
chr5:173953408
|
T | C | 2 | a0001c0001t0015g0307a0001c0001t0025g0308 | 2 | HG01167.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1962+136T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953408 | ||||||
chr5:173953592
|
T | A | 179 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(176): Show | 204 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.1962+320T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953592 | ||||||
chr5:173953726
|
CT | C | 175 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0029others(172): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1962+468delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 173953726 | |||||
chr5:173953891
|
C | T | 6 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0169others(3): Show | 8 | HG02015.hp1 HG02135.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1962+619C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953891 | ||||||
chr5:173953931
|
A | G | 40 | a0001c0001t0004g0001a0001c0001t0004g0034a0001c0001t0004g0269others(37): Show | 46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1962+659A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173953931 | ||||||
chr5:173954172
|
T | G | 3 | a0001c0001t0013g0037a0001c0001t0013g0091a0001c0001t0013g0092 | 3 | HG02451.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1962+900T>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954172 | ||||||
chr5:173954270
|
A | T | 2 | a0001c0001t0004g0269a0001c0001t0004g0280 | 2 | HG00280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1962+998A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954270 | ||||||
chr5:173954497
|
C | T | 2 | a0001c0001t0010g0026a0001c0001t0010g0187 | 3 | HG02630.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1962+1225C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954497 | ||||||
chr5:173954596
|
C | G | 1 | a0001c0001t0002g0180 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1963-1314C>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954596 | ||||||
chr5:173954860
|
G | T | 4 | a0001c0001t0015g0307a0001c0001t0015g0309a0001c0001t0022g0310others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1963-1050G>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954860 | ||||||
chr5:173954945
|
A | T | 1 | a0001c0001t0003g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1963-965A>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954945 | ||||||
chr5:173954946
|
T | A | 18 | a0001c0001t0002g0180a0001c0001t0002g0181a0001c0001t0002g0182others(15): Show | 21 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1963-964T>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954946 | ||||||
chr5:173954971
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1963-939C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173954971 | ||||||
chr5:173955265
|
T | C | 1 | a0001c0002t0018g0010 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1963-645T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955265 | ||||||
chr5:173955338
|
CT | C | 9 | a0001c0001t0002g0214a0001c0001t0002g0221a0001c0001t0004g0279others(6): Show | 9 | HG01167.hp2 HG01517.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1963-557delT | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 173955338 | |||||
chr5:173955445
|
G | C | 1 | a0001c0001t0010g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1963-465G>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955445 | ||||||
chr5:173955474
|
A | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(321): Show | 370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.1963-436A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955474 | ||||||
chr5:173955628
|
T | C | 5 | a0001c0001t0005g0311a0001c0001t0005g0316a0001c0001t0005g0317others(2): Show | 5 | HG00423.hp1 HG00558.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1963-282T>C | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955628 | ||||||
chr5:173955635
|
C | T | 3 | a0001c0001t0003g0154a0001c0001t0006g0153a0001c0001t0006g0155 | 3 | HG02145.hp1 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1963-275C>T | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955635 | ||||||
chr5:173955758
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0015others(70): Show | 86 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1963-152G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955758 | ||||||
chr5:173955774
|
A | G | 19 | a0001c0001t0007g0006a0001c0001t0007g0024a0001c0001t0007g0025others(16): Show | 21 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1963-136A>G | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955774 | ||||||
chr5:173955838
|
G | A | 1 | a0001c0001t0005g0199 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1963-72G>A | CPEB4 | ENSG00000113742.14 | transcript | ENST00000265085.10 | protein_coding | 9/9 | chr5 | 173955838 |