geneid | 1977 |
---|---|
ensemblid | ENSG00000151247.13 |
hgncid | 3287 |
symbol | EIF4E |
name | eukaryotic translation initiation factor 4E |
refseq_nuc | NM_001968.5 |
refseq_prot | NP_001959.1 |
ensembl_nuc | ENST00000450253.7 |
ensembl_prot | ENSP00000389624.2 |
mane_status | MANE Select |
chr | chr4 |
start | 98879276 |
end | 98929133 |
strand | - |
ver | v1.2 |
region | chr4:98879276-98929133 |
region5000 | chr4:98874276-98934133 |
regionname0 | EIF4E_chr4_98879276_98929133 |
regionname5000 | EIF4E_chr4_98874276_98934133 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 217 | 300 | 92 | 56 | 116 | 4 | 30 | 86 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 654 | 283 | 89 | 50 | 116 | 3 | 23 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
c0002 | 0/0 | 654 | 16 | 3 | 6 | 0 | 1 | 6 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
c0003 | 0/0 | 654 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1774 | 205 | 78 | 45 | 59 | 3 | 18 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0002 | 0/0 | 1774 | 60 | 1 | 3 | 51 | 0 | 5 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0003 | 0/0 | 1775 | 14 | 3 | 6 | 0 | 1 | 4 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0004 | 0/0 | 1774 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0005 | 0/0 | 1775 | 6 | 1 | 2 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0006 | 0/0 | 1774 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0007 | 0/0 | 1774 | 3 | 1 | 0 | 0 | 0 | 2 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
t0008 | 0/0 | 1774 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 654 | 283 | 89 | 50 | 116 | 3 | 23 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0002 | 0/0 | 654 | 16 | 3 | 6 | 0 | 1 | 6 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0003 | 0/0 | 654 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2427 | 204 | 78 | 45 | 59 | 3 | 17 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0001t0002 | 0/0 | 2427 | 60 | 1 | 3 | 51 | 0 | 5 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0001t0003 | 0/0 | 2428 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0001t0004 | 0/0 | 2427 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0001t0005 | 0/0 | 2428 | 6 | 1 | 2 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0001t0006 | 0/0 | 2427 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0001t0008 | 0/0 | 2427 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0002t0003 | 0/0 | 2428 | 13 | 2 | 6 | 0 | 1 | 4 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0002t0007 | 0/0 | 2427 | 3 | 1 | 0 | 0 | 0 | 2 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
a0001c0003t0001 | 0/0 | 2427 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | copy fasta | chr4 | 98874276 | 98934133 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0007g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0002t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00423 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00621 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0084 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0083 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0081 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01358 | hp1 | a0001 | c0002 | t0003 | g0088 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0082 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0077 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0199 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0163 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0078 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0079 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0076 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0006 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0006 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03491 | hp2 | a0001 | c0002 | t0007 | g0086 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03492 | hp2 | a0001 | c0002 | t0007 | g0085 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0273 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0087 | SAS | PJL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0161 | SAS | STU | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18987 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | LWK | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19063 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | GIH | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | GIH | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02486 | hp1 | a0001 | c0002 | t0007 | g0080 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0089 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | USA | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0271 | REF | REF | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | EIF4E_chr4_98874276_98934133 | EIF4E | chr4 | 98874276 | 98934133 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:98887103
|
G | A | 1 | a0001c0002 | 16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
synonymous_variant | LOW | c.375C>T | p.Asp125Asp | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/7 | 396/2427 | 375/654 | 125/217 | chr4 | 98887103 | ||
chr4:98901953
|
A | C | 1 | a0001c0003 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.48T>G | p.Thr16Thr | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/7 | 69/2427 | 48/654 | 16/217 | chr4 | 98901953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:98879493
|
G | A | 1 | a0001c0001t0006 | 3 | HG00621.hp1 NA18986.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 1535 | chr4 | 98879493 | |||||
chr4:98879999
|
G | C | 1 | a0001c0001t0008 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1029C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 1029 | chr4 | 98879999 | |||||
chr4:98880282
|
A | G | 3 | a0001c0001t0003a0001c0002t0003a0001c0002t0007 | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*746T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 746 | chr4 | 98880282 | |||||
chr4:98880501
|
G | A | 3 | a0001c0001t0003a0001c0002t0003a0001c0002t0007 | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*527C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 527 | chr4 | 98880501 | |||||
chr4:98880835
|
C | CA | 3 | a0001c0001t0003a0001c0001t0005a0001c0002t0003 | 20 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*192dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 192 | chr4 | 98880835 | |||||
chr4:98880919
|
A | C | 1 | a0001c0001t0002 | 60 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*109T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 7/7 | 109 | chr4 | 98880919 | |||||
chr4:98929133
|
C | G | 1 | a0001c0001t0004 | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/7 | chr4 | 98929133 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:98881158
|
AAAG | A | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.540-19_540-17delCT others(1): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881158 | ||||||
chr4:98881160
|
A | AG | 4 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG03491.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-19dupC | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881160 | ||||||
chr4:98881194
|
A | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.540-52T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881194 | ||||||
chr4:98881244
|
C | T | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 216 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.540-102G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881244 | ||||||
chr4:98881281
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.540-139G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881281 | ||||||
chr4:98881542
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540-400A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881542 | ||||||
chr4:98881583
|
G | GTTTAT | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 133 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(130): Show |
intron_variant | MODIFIER | c.540-442_540-441ins others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881583 | ||||||
chr4:98881709
|
G | A | 1 | a0001c0001t0005g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.540-567C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881709 | ||||||
chr4:98881725
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.540-583G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881725 | ||||||
chr4:98881800
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.540-658T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881800 | ||||||
chr4:98881866
|
G | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.540-724C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881866 | ||||||
chr4:98881949
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0268 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.540-807T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98881949 | ||||||
chr4:98882100
|
T | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 78 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.540-958A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882100 | ||||||
chr4:98882336
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540-1194C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882336 | ||||||
chr4:98882396
|
CA | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(188): Show | 209 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.540-1255delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882396 | ||||||
chr4:98882532
|
GT | G | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-1391delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882532 | ||||||
chr4:98882575
|
A | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-1433T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882575 | ||||||
chr4:98882703
|
T | C | 1 | a0001c0001t0005g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.540-1561A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882703 | ||||||
chr4:98882862
|
T | C | 3 | a0001c0002t0003g0083a0001c0002t0003g0088a0001c0002t0003g0089 | 3 | HG01081.hp1 HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.540-1720A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882862 | ||||||
chr4:98882947
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.540-1805C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98882947 | ||||||
chr4:98883129
|
T | C | 3 | a0001c0002t0003g0076a0001c0002t0003g0077a0001c0002t0003g0084 | 3 | HG00733.hp2 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.539+1793A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883129 | ||||||
chr4:98883166
|
G | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.539+1756C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883166 | ||||||
chr4:98883172
|
TGA | T | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+1748_539+1749d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883172 | ||||||
chr4:98883228
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.539+1694G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883228 | ||||||
chr4:98883242
|
A | T | 1 | a0001c0001t0001g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.539+1680T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883242 | ||||||
chr4:98883275
|
AAATT | A | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+1643_539+1646d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883275 | ||||||
chr4:98883333
|
A | C | 1 | a0001c0001t0002g0023 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.539+1589T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883333 | ||||||
chr4:98883335
|
C | A | 1 | a0001c0001t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.539+1587G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883335 | ||||||
chr4:98883392
|
A | AT | 2 | a0001c0001t0001g0007a0001c0001t0001g0107 | 3 | HG01515.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.539+1529_539+1530i others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883392 | ||||||
chr4:98883393
|
A | AT | 191 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(188): Show | 207 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.539+1528dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | ||||||
chr4:98883393
|
A | ATT | 51 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0047others(48): Show | 53 | HG00621.hp1 HG00733.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+1527_539+1528d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | ||||||
chr4:98883393
|
A | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0110 | 4 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+1529T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | ||||||
chr4:98883393
|
ATTTTTT | A | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.539+1523_539+1528d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883393 | ||||||
chr4:98883596
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.539+1326C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883596 | ||||||
chr4:98883605
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.539+1317C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883605 | ||||||
chr4:98883703
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.539+1219A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883703 | ||||||
chr4:98883739
|
C | CTTAG | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.539+1179_539+1182d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98883739 | ||||||
chr4:98884038
|
C | CA | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 97 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.539+883dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884038 | ||||||
chr4:98884292
|
G | A | 1 | a0001c0002t0003g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.539+630C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884292 | ||||||
chr4:98884461
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0130 | 2 | HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.539+461C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884461 | ||||||
chr4:98884511
|
C | G | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.539+411G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884511 | ||||||
chr4:98884514
|
G | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.539+408C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884514 | ||||||
chr4:98884703
|
A | C | 20 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0207others(17): Show | 20 | HG00673.hp1 HG01243.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.539+219T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884703 | ||||||
chr4:98884732
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.539+190A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884732 | ||||||
chr4:98884744
|
C | CA | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.539+177dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884744 | ||||||
chr4:98884763
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.539+159C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 6/6 | chr4 | 98884763 | ||||||
chr4:98885095
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.400-34A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885095 | ||||||
chr4:98885364
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-303A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885364 | ||||||
chr4:98885390
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.400-329G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885390 | ||||||
chr4:98885475
|
T | C | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-414A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885475 | ||||||
chr4:98885479
|
G | C | 1 | a0001c0001t0001g0007 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.400-418C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98885479 | ||||||
chr4:98886056
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.400-995C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886056 | ||||||
chr4:98886525
|
G | A | 1 | a0001c0001t0005g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.399+554C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886525 | ||||||
chr4:98886531
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.399+548A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886531 | ||||||
chr4:98886723
|
A | G | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+356T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886723 | ||||||
chr4:98886727
|
G | A | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.399+352C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886727 | ||||||
chr4:98886817
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.399+262C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886817 | ||||||
chr4:98886923
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 18 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.399+156C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886923 | ||||||
chr4:98886931
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.399+148A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886931 | ||||||
chr4:98886985
|
CTTAAA | C | 15 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(12): Show | 16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.399+89_399+93delTT others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 5/6 | chr4 | 98886985 | ||||||
chr4:98887380
|
C | G | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-188G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887380 | ||||||
chr4:98887542
|
T | C | 279 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 298 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(295): Show |
intron_variant | MODIFIER | c.285+347A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887542 | ||||||
chr4:98887619
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.285+270C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887619 | ||||||
chr4:98887628
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.285+261T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887628 | ||||||
chr4:98887654
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.285+235T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887654 | ||||||
chr4:98887721
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.285+168A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 4/6 | chr4 | 98887721 | ||||||
chr4:98887990
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.222-38A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98887990 | ||||||
chr4:98888025
|
A | T | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-73T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888025 | ||||||
chr4:98888271
|
G | A | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-319C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888271 | ||||||
chr4:98888321
|
AAAAAAC | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0108a0001c0001t0001g0110others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-375_222-370del others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888321 | ||||||
chr4:98888350
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.222-398T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888350 | ||||||
chr4:98888438
|
C | T | 15 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(12): Show | 16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.222-486G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888438 | ||||||
chr4:98888546
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.222-594C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888546 | ||||||
chr4:98888677
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-725A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888677 | ||||||
chr4:98888952
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.222-1000T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888952 | ||||||
chr4:98888957
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.222-1005C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98888957 | ||||||
chr4:98889157
|
C | CA | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-1206dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889157 | ||||||
chr4:98889157
|
CA | C | 81 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 85 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.222-1206delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889157 | ||||||
chr4:98889340
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0110others(1): Show | 5 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.222-1388C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889340 | ||||||
chr4:98889359
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222-1407T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889359 | ||||||
chr4:98889406
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.222-1454G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889406 | ||||||
chr4:98889654
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.221+1583A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889654 | ||||||
chr4:98889804
|
CCT | C | 7 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0221others(4): Show | 7 | NA18952.hp2 NA18965.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+1431_221+1432d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889804 | ||||||
chr4:98889839
|
T | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0002t0007g0080 | 3 | HG02486.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.221+1398A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889839 | ||||||
chr4:98889844
|
G | A | 3 | a0001c0002t0003g0076a0001c0002t0003g0077a0001c0002t0003g0084 | 3 | HG00733.hp2 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.221+1393C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889844 | ||||||
chr4:98889889
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+1348A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98889889 | ||||||
chr4:98890018
|
A | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.221+1219T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890018 | ||||||
chr4:98890771
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.221+466A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890771 | ||||||
chr4:98890785
|
G | C | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 132 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(129): Show |
intron_variant | MODIFIER | c.221+452C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890785 | ||||||
chr4:98890832
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0129 | 2 | NA18948.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.221+405T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890832 | ||||||
chr4:98890836
|
C | T | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.221+401G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98890836 | ||||||
chr4:98891149
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.221+88G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 3/6 | chr4 | 98891149 | ||||||
chr4:98891645
|
C | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-313G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98891645 | ||||||
chr4:98892104
|
T | C | 1 | a0001c0001t0004g0188 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.126-772A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892104 | ||||||
chr4:98892115
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126-783C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892115 | ||||||
chr4:98892143
|
T | C | 1 | a0001c0002t0003g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-811A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892143 | ||||||
chr4:98892252
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-920T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892252 | ||||||
chr4:98892277
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0178others(3): Show | 6 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-945G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892277 | ||||||
chr4:98892327
|
AC | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 112 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(109): Show |
intron_variant | MODIFIER | c.126-996delG | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892327 | ||||||
chr4:98892328
|
C | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0072a0001c0001t0001g0096others(15): Show | 18 | HG01081.hp1 HG01123.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.126-996G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892328 | ||||||
chr4:98892335
|
A | C | 15 | a0001c0001t0001g0011a0001c0001t0001g0072a0001c0001t0001g0096others(12): Show | 15 | HG01081.hp1 HG01123.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.126-1003T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892335 | ||||||
chr4:98892337
|
A | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 116 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.126-1005T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892337 | ||||||
chr4:98892340
|
C | A | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 131 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(128): Show |
intron_variant | MODIFIER | c.126-1008G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892340 | ||||||
chr4:98892344
|
A | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(66): Show | 83 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.126-1012T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892344 | ||||||
chr4:98892352
|
A | C | 1 | a0001c0001t0005g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.126-1020T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892352 | ||||||
chr4:98892353
|
C | A | 1 | a0001c0001t0005g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.126-1021G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892353 | ||||||
chr4:98892357
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-1025T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892357 | ||||||
chr4:98892453
|
C | T | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-1121G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892453 | ||||||
chr4:98892477
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.126-1145C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892477 | ||||||
chr4:98892498
|
G | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.126-1166C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892498 | ||||||
chr4:98892553
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-1221C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892553 | ||||||
chr4:98892609
|
G | C | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.126-1277C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892609 | ||||||
chr4:98892610
|
T | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-1278A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892610 | ||||||
chr4:98892681
|
C | CA | 8 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0248others(5): Show | 8 | HG01074.hp2 HG01934.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-1350dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892681 | ||||||
chr4:98892681
|
CA | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0093others(24): Show | 28 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.126-1350delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892681 | ||||||
chr4:98892681
|
CAA | C | 165 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 182 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.126-1351_126-1350d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892681 | ||||||
chr4:98892888
|
A | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG00423.hp2 NA18955.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.126-1556T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98892888 | ||||||
chr4:98893032
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.126-1700T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893032 | ||||||
chr4:98893147
|
TA | T | 8 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0077others(5): Show | 9 | HG01358.hp1 HG01515.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-1816delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893147 | ||||||
chr4:98893148
|
A | AAAAAAAA others(3301): Show |
2 | a0001c0002t0003g0076a0001c0002t0003g0084 | 2 | HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.126-1817_126-1816i others(3310): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893148 | ||||||
chr4:98893148
|
A | AAAAAAAA others(3301): Show |
5 | a0001c0002t0003g0081a0001c0002t0003g0082a0001c0002t0003g0083others(2): Show | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-1817_126-1816i others(3310): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893148 | ||||||
chr4:98893148
|
A | AAAAAAAA others(3301): Show |
1 | a0001c0002t0003g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-1817_126-1816i others(3310): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893148 | ||||||
chr4:98893163
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.126-1831A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893163 | ||||||
chr4:98893165
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-1833G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893165 | ||||||
chr4:98893258
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126-1926G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893258 | ||||||
chr4:98893291
|
T | C | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.126-1959A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893291 | ||||||
chr4:98893366
|
T | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-2034A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893366 | ||||||
chr4:98893379
|
T | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-2047A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893379 | ||||||
chr4:98893393
|
T | C | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.126-2061A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893393 | ||||||
chr4:98893470
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.126-2138C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893470 | ||||||
chr4:98893728
|
C | CGGGTTGG others(3302): Show |
1 | a0001c0002t0003g0077 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.126-2397_126-2396i others(3311): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893728 | ||||||
chr4:98893763
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.126-2431A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893763 | ||||||
chr4:98893852
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126-2520A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893852 | ||||||
chr4:98893907
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-2575A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98893907 | ||||||
chr4:98894035
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126-2703C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98894035 | ||||||
chr4:98894096
|
C | T | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-2764G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98894096 | ||||||
chr4:98894799
|
T | C | 8 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0142others(5): Show | 8 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-3467A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98894799 | ||||||
chr4:98895008
|
G | A | 1 | a0001c0002t0003g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.126-3676C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895008 | ||||||
chr4:98895076
|
C | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 216 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.126-3744G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895076 | ||||||
chr4:98895156
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.126-3824T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895156 | ||||||
chr4:98895198
|
G | A | 34 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(31): Show | 35 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.126-3866C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895198 | ||||||
chr4:98895319
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-3987G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895319 | ||||||
chr4:98895370
|
A | G | 1 | a0001c0002t0003g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-4038T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895370 | ||||||
chr4:98895590
|
A | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0005g0199others(1): Show | 4 | HG01943.hp1 HG01975.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-4258T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895590 | ||||||
chr4:98895674
|
G | C | 1 | a0001c0001t0002g0037 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126-4342C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895674 | ||||||
chr4:98895982
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 70 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.126-4650C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895982 | ||||||
chr4:98895984
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126-4652A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895984 | ||||||
chr4:98895990
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.126-4658C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98895990 | ||||||
chr4:98896020
|
ACC | A | 17 | a0001c0001t0001g0072a0001c0001t0003g0091a0001c0002t0003g0006others(14): Show | 18 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.126-4690_126-4689d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896020 | ||||||
chr4:98896025
|
G | A | 3 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0254 | 3 | HG00621.hp1 NA18986.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.126-4693C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896025 | ||||||
chr4:98896068
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.126-4736G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896068 | ||||||
chr4:98896111
|
G | A | 8 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0142others(5): Show | 8 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-4779C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896111 | ||||||
chr4:98896128
|
G | A | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-4796C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896128 | ||||||
chr4:98896150
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(3): Show | 6 | HG01261.hp2 HG01934.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-4818G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896150 | ||||||
chr4:98896195
|
C | CAATAA | 6 | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0001g0120others(3): Show | 6 | HG01109.hp1 HG01109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-4868_126-4864d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896195 | ||||||
chr4:98896224
|
A | AAAATAAA others(98): Show |
1 | a0001c0001t0001g0195 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(107): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(93): Show |
1 | a0001c0001t0001g0194 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(102): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(83): Show |
1 | a0001c0001t0004g0185 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.126-4893_126-4892i others(92): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(53): Show |
1 | a0001c0001t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(62): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(43): Show |
1 | a0001c0001t0001g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126-4893_126-4892i others(52): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(38): Show |
13 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0177others(10): Show | 13 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-4893_126-4892i others(47): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(33): Show |
4 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0004g0173others(1): Show | 4 | HG02622.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-4893_126-4892i others(42): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(28): Show |
1 | a0001c0001t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126-4893_126-4892i others(37): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(23): Show |
1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126-4893_126-4892i others(32): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896224
|
A | AAAATAAA others(13): Show |
2 | a0001c0001t0001g0181a0001c0001t0001g0183 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.126-4893_126-4892i others(22): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896224 | ||||||
chr4:98896363
|
C | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 70 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.126-5031G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896363 | ||||||
chr4:98896486
|
C | CA | 104 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0056others(101): Show | 117 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.126-5155dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896486
|
C | CAA | 40 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0074others(37): Show | 43 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.126-5156_126-5155d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896486
|
C | CAAA | 7 | a0001c0001t0001g0072a0001c0001t0001g0090a0001c0001t0001g0145others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-5157_126-5155d others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896486
|
C | CAAAAA | 9 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0092others(6): Show | 9 | HG01123.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.126-5159_126-5155d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896486
|
C | CAAAAAA | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0004g0185others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-5160_126-5155d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896486
|
C | CAAAAAAA | 10 | a0001c0001t0001g0095a0001c0001t0001g0174a0001c0001t0001g0175others(7): Show | 10 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.126-5161_126-5155d others(9): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896486
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0100a0001c0001t0001g0176a0001c0001t0001g0181others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-5162_126-5155d others(10): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896486 | ||||||
chr4:98896502
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.126-5170T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896502 | ||||||
chr4:98896667
|
C | CA | 33 | a0001c0001t0001g0200a0001c0001t0001g0206a0001c0001t0001g0207others(30): Show | 33 | HG00423.hp2 HG00621.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.125+5208dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896667
|
CAA | C | 30 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(27): Show | 31 | HG00673.hp2 HG01884.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.125+5207_125+5208d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896667
|
CAAA | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(86): Show | 104 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.125+5206_125+5208d others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896667
|
CAAAA | C | 9 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0120others(6): Show | 9 | HG01109.hp2 HG01934.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.125+5205_125+5208d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896667
|
CAAAAA | C | 28 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0093others(25): Show | 29 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.125+5204_125+5208d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896667
|
CAAAAAA | C | 22 | a0001c0001t0001g0096a0001c0001t0001g0174a0001c0001t0001g0175others(19): Show | 22 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.125+5203_125+5208d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896667
|
CAAAAAAA others(6): Show |
C | 18 | a0001c0001t0001g0008a0001c0001t0001g0121a0001c0001t0001g0122others(15): Show | 19 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.125+5196_125+5208d others(15): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896667 | ||||||
chr4:98896738
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+5138C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896738 | ||||||
chr4:98896801
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+5075G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896801 | ||||||
chr4:98896918
|
C | T | 1 | a0001c0002t0007g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125+4958G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896918 | ||||||
chr4:98896946
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125+4930G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896946 | ||||||
chr4:98896972
|
C | T | 6 | a0001c0002t0003g0076a0001c0002t0003g0077a0001c0002t0003g0083others(3): Show | 6 | HG00733.hp2 HG01081.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+4904G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98896972 | ||||||
chr4:98897108
|
G | T | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+4768C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897108 | ||||||
chr4:98897275
|
T | TAAGAATG others(311): Show |
22 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(19): Show | 22 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.125+4600_125+4601i others(320): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897275 | ||||||
chr4:98897275
|
T | TAAGAATG others(312): Show |
4 | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0193others(1): Show | 4 | HG00735.hp1 HG02145.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+4600_125+4601i others(321): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897275 | ||||||
chr4:98897318
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 133 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(130): Show |
intron_variant | MODIFIER | c.125+4558A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897318 | ||||||
chr4:98897482
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+4394T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897482 | ||||||
chr4:98897497
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.125+4379G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897497 | ||||||
chr4:98897670
|
T | C | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+4206A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897670 | ||||||
chr4:98897682
|
A | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 216 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.125+4194T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897682 | ||||||
chr4:98897807
|
A | G | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+4069T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98897807 | ||||||
chr4:98898123
|
GA | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01070.hp2 HG01243.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+3752delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898123 | ||||||
chr4:98898124
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.125+3752T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898124 | ||||||
chr4:98898238
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.125+3638A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898238 | ||||||
chr4:98898429
|
A | G | 5 | a0001c0001t0001g0243a0001c0001t0001g0248a0001c0001t0001g0265others(2): Show | 5 | HG01074.hp2 HG01123.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+3447T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898429 | ||||||
chr4:98898448
|
A | C | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+3428T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898448 | ||||||
chr4:98898465
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 70 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.125+3411C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898465 | ||||||
chr4:98898492
|
C | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.125+3384G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898492 | ||||||
chr4:98898533
|
G | A | 1 | a0001c0002t0003g0006 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.125+3343C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898533 | ||||||
chr4:98898782
|
A | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0214a0001c0001t0001g0250others(3): Show | 6 | HG02027.hp2 HG02083.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+3094T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898782 | ||||||
chr4:98898897
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+2979A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898897 | ||||||
chr4:98898916
|
G | A | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+2960C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98898916 | ||||||
chr4:98899054
|
T | TA | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0160others(4): Show | 7 | HG01168.hp1 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+2821dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899054 | ||||||
chr4:98899054
|
TA | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0004g0173others(8): Show | 11 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+2821delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899054 | ||||||
chr4:98899105
|
T | A | 13 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(10): Show | 14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.125+2771A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899105 | ||||||
chr4:98899209
|
T | C | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+2667A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899209 | ||||||
chr4:98899318
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+2558A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899318 | ||||||
chr4:98899389
|
G | A | 17 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.125+2487C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899389 | ||||||
chr4:98899396
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.125+2480T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899396 | ||||||
chr4:98899427
|
A | C | 2 | a0001c0001t0006g0234a0001c0001t0006g0254 | 2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.125+2449T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899427 | ||||||
chr4:98899456
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.125+2420C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899456 | ||||||
chr4:98899819
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.125+2057A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899819 | ||||||
chr4:98899883
|
T | C | 1 | a0001c0002t0003g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.125+1993A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899883 | ||||||
chr4:98899945
|
T | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+1931A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98899945 | ||||||
chr4:98900048
|
T | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.125+1828A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900048 | ||||||
chr4:98900313
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0107others(44): Show | 49 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.125+1563G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900313 | ||||||
chr4:98900462
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+1414T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900462 | ||||||
chr4:98900471
|
G | A | 199 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(196): Show | 217 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.125+1405C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900471 | ||||||
chr4:98900478
|
TA | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.125+1397delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900478 | ||||||
chr4:98900518
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.125+1358C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900518 | ||||||
chr4:98900525
|
CTT | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+1349_125+1350d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900525 | ||||||
chr4:98900634
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.125+1242G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900634 | ||||||
chr4:98900825
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 78 | HG00558.hp2 HG00733.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.125+1051T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900825 | ||||||
chr4:98900902
|
C | T | 1 | a0001c0002t0003g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.125+974G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98900902 | ||||||
chr4:98901030
|
T | C | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+846A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901030 | ||||||
chr4:98901120
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+756A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901120 | ||||||
chr4:98901123
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+753G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901123 | ||||||
chr4:98901200
|
C | CT | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.125+675dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901200 | ||||||
chr4:98901259
|
G | A | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.125+617C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901259 | ||||||
chr4:98901323
|
G | A | 1 | a0001c0002t0007g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125+553C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901323 | ||||||
chr4:98901436
|
T | G | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+440A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901436 | ||||||
chr4:98901443
|
CCCGCCT | C | 10 | a0001c0001t0001g0011a0001c0001t0001g0072a0001c0001t0001g0102others(7): Show | 10 | HG00735.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.125+427_125+432del others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901443 | ||||||
chr4:98901491
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.125+385C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901491 | ||||||
chr4:98901754
|
T | C | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.125+122A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 2/6 | chr4 | 98901754 | ||||||
chr4:98902030
|
T | C | 7 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0248others(4): Show | 7 | HG01074.hp2 HG01123.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-48A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902030 | ||||||
chr4:98902159
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19-177G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902159 | ||||||
chr4:98902376
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-394C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902376 | ||||||
chr4:98902391
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19-409T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902391 | ||||||
chr4:98902554
|
T | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0107others(44): Show | 49 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.19-572A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902554 | ||||||
chr4:98902620
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.19-638A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902620 | ||||||
chr4:98902640
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-658C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902640 | ||||||
chr4:98902864
|
CA | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-883delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98902864 | ||||||
chr4:98903049
|
A | G | 1 | a0001c0002t0003g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19-1067T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903049 | ||||||
chr4:98903210
|
A | G | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-1228T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903210 | ||||||
chr4:98903275
|
C | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-1293G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903275 | ||||||
chr4:98903360
|
G | GT | 16 | a0001c0001t0001g0174a0001c0001t0001g0275a0001c0001t0002g0027others(13): Show | 17 | HG00735.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-1379dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903360 | ||||||
chr4:98903435
|
T | C | 35 | a0001c0001t0001g0060a0001c0001t0001g0073a0001c0001t0002g0001others(32): Show | 48 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.19-1453A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903435 | ||||||
chr4:98903452
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.19-1470A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903452 | ||||||
chr4:98903486
|
T | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-1504A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903486 | ||||||
chr4:98903514
|
T | C | 13 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(10): Show | 14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-1532A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903514 | ||||||
chr4:98903677
|
G | A | 3 | a0001c0002t0003g0006a0001c0002t0007g0085a0001c0002t0007g0086 | 4 | HG03017.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1695C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98903677 | ||||||
chr4:98904122
|
GAGA | G | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-2143_19-2141del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904122 | ||||||
chr4:98904455
|
AT | A | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-2474delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904455 | ||||||
chr4:98904488
|
C | T | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-2506G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904488 | ||||||
chr4:98904502
|
G | A | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-2520C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904502 | ||||||
chr4:98904552
|
C | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19-2570G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904552 | ||||||
chr4:98904640
|
A | G | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 132 | HG00558.hp2 HG00733.hp1 HG00733.hp2 others(129): Show |
intron_variant | MODIFIER | c.19-2658T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904640 | ||||||
chr4:98904643
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-2661G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904643 | ||||||
chr4:98904831
|
T | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-2849A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98904831 | ||||||
chr4:98905096
|
G | T | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-3114C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905096 | ||||||
chr4:98905206
|
C | T | 17 | a0001c0001t0001g0072a0001c0001t0003g0091a0001c0002t0003g0006others(14): Show | 18 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-3224G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905206 | ||||||
chr4:98905231
|
T | TAA | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(68): Show | 74 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.19-3251_19-3250dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905231 | ||||||
chr4:98905231
|
TA | T | 28 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(25): Show | 28 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.19-3250delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905231 | ||||||
chr4:98905233
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-3251T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905233 | ||||||
chr4:98905416
|
G | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-3434C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905416 | ||||||
chr4:98905432
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19-3450G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905432 | ||||||
chr4:98905727
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.19-3745G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98905727 | ||||||
chr4:98906163
|
T | A | 1 | a0001c0001t0006g0254 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-4181A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906163 | ||||||
chr4:98906264
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-4282C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906264 | ||||||
chr4:98906509
|
A | G | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-4527T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906509 | ||||||
chr4:98906642
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.19-4660G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906642 | ||||||
chr4:98906651
|
C | T | 15 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(12): Show | 16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.19-4669G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906651 | ||||||
chr4:98906796
|
C | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-4814G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906796 | ||||||
chr4:98906888
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-4906A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906888 | ||||||
chr4:98906956
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.19-4974A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98906956 | ||||||
chr4:98907176
|
A | G | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-5194T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907176 | ||||||
chr4:98907217
|
A | G | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-5235T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907217 | ||||||
chr4:98907396
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 5 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-5414G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907396 | ||||||
chr4:98907431
|
T | TCAAAAAA others(4): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-5460_19-5450dup others(11): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907431 | ||||||
chr4:98907523
|
T | C | 1 | a0001c0002t0003g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-5541A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907523 | ||||||
chr4:98907605
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19-5623C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907605 | ||||||
chr4:98907755
|
T | A | 1 | a0001c0001t0006g0235 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-5773A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907755 | ||||||
chr4:98907855
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-5873T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98907855 | ||||||
chr4:98908103
|
A | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-6121T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908103 | ||||||
chr4:98908154
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.19-6172G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908154 | ||||||
chr4:98908224
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-6242T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908224 | ||||||
chr4:98908525
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-6543A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908525 | ||||||
chr4:98908711
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-6729G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908711 | ||||||
chr4:98908815
|
C | G | 64 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(61): Show | 78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-6833G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98908815 | ||||||
chr4:98909114
|
G | A | 17 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-7132C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909114 | ||||||
chr4:98909203
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-7221C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909203 | ||||||
chr4:98909528
|
A | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-7546T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909528 | ||||||
chr4:98909689
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-7707C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909689 | ||||||
chr4:98909855
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.19-7873G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909855 | ||||||
chr4:98909943
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-7961G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98909943 | ||||||
chr4:98910153
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-8171A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910153 | ||||||
chr4:98910311
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096 | 3 | HG02809.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.19-8329C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910311 | ||||||
chr4:98910349
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19-8367T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910349 | ||||||
chr4:98910383
|
A | C | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-8401T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910383 | ||||||
chr4:98910458
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19-8476A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910458 | ||||||
chr4:98910508
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-8526T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910508 | ||||||
chr4:98910704
|
A | C | 3 | a0001c0001t0006g0234a0001c0001t0006g0235a0001c0001t0006g0254 | 3 | HG00621.hp1 NA18986.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.19-8722T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910704 | ||||||
chr4:98910734
|
C | CT | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 70 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.19-8753dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910734 | ||||||
chr4:98910799
|
G | A | 17 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-8817C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910799 | ||||||
chr4:98910832
|
C | G | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-8850G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910832 | ||||||
chr4:98910854
|
C | G | 1 | a0001c0001t0002g0013 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.19-8872G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910854 | ||||||
chr4:98910919
|
C | T | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-8937G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910919 | ||||||
chr4:98910943
|
C | G | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-8961G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98910943 | ||||||
chr4:98911016
|
G | A | 17 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(14): Show | 17 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-9034C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911016 | ||||||
chr4:98911022
|
C | T | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-9040G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911022 | ||||||
chr4:98911193
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG01070.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-9211G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911193 | ||||||
chr4:98911195
|
C | T | 13 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(10): Show | 14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-9213G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911195 | ||||||
chr4:98911206
|
G | A | 1 | a0001c0002t0007g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-9224C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911206 | ||||||
chr4:98911210
|
G | A | 17 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-9228C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911210 | ||||||
chr4:98911221
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-9239C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911221 | ||||||
chr4:98911294
|
C | T | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-9312G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911294 | ||||||
chr4:98911426
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-9444C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911426 | ||||||
chr4:98911489
|
A | G | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.19-9507T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911489 | ||||||
chr4:98911583
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-9601G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911583 | ||||||
chr4:98911661
|
C | CA | 19 | a0001c0001t0001g0072a0001c0001t0001g0090a0001c0001t0001g0121others(16): Show | 19 | HG01069.hp1 HG01168.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.19-9680dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
C | CAA | 48 | a0001c0001t0001g0008a0001c0001t0001g0108a0001c0001t0001g0109others(45): Show | 49 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.19-9681_19-9680dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
C | CAAA | 8 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0113others(5): Show | 8 | HG00733.hp1 HG02074.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-9682_19-9680dup others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
C | CAAAA | 4 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0168others(1): Show | 6 | HG01515.hp1 HG01517.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-9683_19-9680dup others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
CA | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(73): Show | 90 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.19-9680delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
CAA | C | 27 | a0001c0001t0001g0011a0001c0001t0001g0047a0001c0001t0001g0075others(24): Show | 28 | HG00733.hp2 HG01081.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.19-9681_19-9680del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
CAAA | C | 9 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG01496.hp1 HG02647.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-9682_19-9680del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.19-9692_19-9680del others(13): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911661
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19-9693_19-9680del others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911661 | ||||||
chr4:98911979
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.19-9997C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911979 | ||||||
chr4:98911992
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.19-10010G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98911992 | ||||||
chr4:98912177
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-10195C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912177 | ||||||
chr4:98912228
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-10246C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912228 | ||||||
chr4:98912269
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-10287T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912269 | ||||||
chr4:98912470
|
G | A | 1 | a0001c0001t0004g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.19-10488C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912470 | ||||||
chr4:98912524
|
T | C | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.19-10542A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912524 | ||||||
chr4:98912525
|
G | A | 13 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(10): Show | 14 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-10543C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912525 | ||||||
chr4:98912586
|
CAAAGA | C | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0075others(43): Show | 48 | HG00558.hp2 HG00733.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.19-10609_19-10605d others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912586 | ||||||
chr4:98912636
|
A | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.19-10654T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912636 | ||||||
chr4:98912636
|
AT | A | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-10655delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912636 | ||||||
chr4:98912763
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19-10781A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912763 | ||||||
chr4:98912929
|
G | A | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-10947C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98912929 | ||||||
chr4:98913081
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.19-11099C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913081 | ||||||
chr4:98913098
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.19-11116G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913098 | ||||||
chr4:98913099
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-11117C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913099 | ||||||
chr4:98913130
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.19-11148G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913130 | ||||||
chr4:98913207
|
C | CA | 9 | a0001c0001t0001g0075a0001c0001t0004g0173a0001c0001t0004g0185others(6): Show | 9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-11226dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913207 | ||||||
chr4:98913207
|
CA | C | 17 | a0001c0001t0001g0260a0001c0001t0001g0268a0001c0002t0003g0006others(14): Show | 18 | HG00733.hp2 HG01081.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.19-11226delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913207 | ||||||
chr4:98913226
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.19-11244T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913226 | ||||||
chr4:98913324
|
T | G | 1 | a0001c0002t0007g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-11342A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913324 | ||||||
chr4:98913436
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0262 | 2 | HG00673.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.19-11454G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913436 | ||||||
chr4:98913802
|
A | C | 1 | a0001c0001t0006g0235 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-11820T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913802 | ||||||
chr4:98913859
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19-11877A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913859 | ||||||
chr4:98913964
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.19-11982G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98913964 | ||||||
chr4:98914033
|
C | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-12051G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914033 | ||||||
chr4:98914064
|
TA | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-12083delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914064 | ||||||
chr4:98914228
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-12246A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914228 | ||||||
chr4:98914274
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19-12292A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914274 | ||||||
chr4:98914337
|
T | TG | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-12356dupC | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914337 | ||||||
chr4:98914361
|
C | CA | 21 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0059others(18): Show | 21 | HG01192.hp1 HG01243.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-12380dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
C | CAA | 6 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG01123.hp2 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-12381_19-12380d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.19-12391_19-12380d others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0003g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-12393_19-12380d others(16): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0003g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-12398_19-12380d others(21): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
C | CAAAAAAA others(34): Show |
1 | a0001c0002t0007g0080 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-12380_19-12379i others(43): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
CA | C | 111 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0045others(108): Show | 125 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.19-12380delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
CAA | C | 62 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0107others(59): Show | 64 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.19-12381_19-12380d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914361
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG02647.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-12389_19-12380d others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914361 | ||||||
chr4:98914392
|
CT | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 71 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.19-12411delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914392 | ||||||
chr4:98914508
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19-12526C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914508 | ||||||
chr4:98914655
|
T | G | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096 | 3 | HG02809.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.19-12673A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914655 | ||||||
chr4:98914810
|
A | G | 1 | a0001c0002t0003g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.19-12828T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914810 | ||||||
chr4:98914860
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.19-12878C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98914860 | ||||||
chr4:98915002
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.19-13020C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915002 | ||||||
chr4:98915017
|
C | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.19-13035G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915017 | ||||||
chr4:98915099
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19-13117T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915099 | ||||||
chr4:98915253
|
G | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-13271C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915253 | ||||||
chr4:98915256
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.19-13274G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915256 | ||||||
chr4:98915387
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(66): Show | 83 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.19-13405T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915387 | ||||||
chr4:98915545
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+13539_18+13549d others(13): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915545 | ||||||
chr4:98915601
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.18+13494G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915601 | ||||||
chr4:98915645
|
A | G | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+13450T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915645 | ||||||
chr4:98915659
|
A | G | 64 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(61): Show | 78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.18+13436T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915659 | ||||||
chr4:98915690
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+13405C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915690 | ||||||
chr4:98915732
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.18+13363C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98915732 | ||||||
chr4:98916020
|
G | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+13075C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916020 | ||||||
chr4:98916083
|
C | T | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+13012G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916083 | ||||||
chr4:98916206
|
G | A | 1 | a0001c0002t0003g0087 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.18+12889C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916206 | ||||||
chr4:98916254
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.18+12841T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916254 | ||||||
chr4:98916286
|
C | CA | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(102): Show | 108 | HG00558.hp2 HG00733.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.18+12808dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916286 | ||||||
chr4:98916286
|
C | CAA | 83 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(80): Show | 98 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.18+12807_18+12808d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916286 | ||||||
chr4:98916286
|
CA | C | 9 | a0001c0001t0001g0281a0001c0001t0004g0173a0001c0001t0004g0185others(6): Show | 9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12808delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916286 | ||||||
chr4:98916310
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+12785T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916310 | ||||||
chr4:98916348
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+12747G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916348 | ||||||
chr4:98916410
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12685G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916410 | ||||||
chr4:98916493
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+12602C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916493 | ||||||
chr4:98916534
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12561A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916534 | ||||||
chr4:98916578
|
G | A | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12517C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916578 | ||||||
chr4:98916661
|
G | T | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12434C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916661 | ||||||
chr4:98916751
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.18+12344T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916751 | ||||||
chr4:98916768
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12327A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98916768 | ||||||
chr4:98917005
|
A | G | 1 | a0001c0001t0003g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.18+12090T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917005 | ||||||
chr4:98917083
|
A | AAC | 8 | a0001c0001t0001g0162a0001c0001t0001g0237a0001c0001t0001g0240others(5): Show | 8 | HG00735.hp2 HG01891.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12010_18+12011d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | ||||||
chr4:98917083
|
A | AACAC | 4 | a0001c0001t0001g0046a0001c0001t0001g0233a0001c0001t0001g0261others(1): Show | 4 | HG00673.hp1 HG02040.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12008_18+12011d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | ||||||
chr4:98917083
|
AAC | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0229a0001c0001t0001g0230others(3): Show | 6 | HG01167.hp1 HG01346.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+12010_18+12011d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | ||||||
chr4:98917083
|
AACAC | A | 8 | a0001c0001t0001g0206a0001c0001t0001g0250a0001c0001t0001g0251others(5): Show | 8 | HG00423.hp2 HG01123.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+12008_18+12011d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | ||||||
chr4:98917083
|
AACACAC | A | 4 | a0001c0001t0001g0208a0001c0001t0001g0252a0001c0001t0001g0260others(1): Show | 4 | HG01168.hp2 HG03834.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+12006_18+12011d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917083 | ||||||
chr4:98917109
|
CACACACA others(21): Show |
C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+11958_18+11985d others(30): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917109 | ||||||
chr4:98917113
|
CACACACA others(17): Show |
C | 2 | a0001c0001t0001g0011a0001c0001t0002g0039 | 2 | HG01123.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.18+11958_18+11981d others(26): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917113 | ||||||
chr4:98917115
|
CACACACA others(15): Show |
C | 16 | a0001c0001t0001g0198a0001c0001t0003g0091a0001c0002t0003g0006others(13): Show | 17 | HG01081.hp1 HG01192.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+11958_18+11979d others(24): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917115 | ||||||
chr4:98917117
|
CACACACA others(13): Show |
C | 7 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0115others(4): Show | 8 | HG00733.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+11958_18+11977d others(22): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917117 | ||||||
chr4:98917119
|
CACACACA others(11): Show |
C | 8 | a0001c0001t0001g0075a0001c0001t0004g0173a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+11958_18+11975d others(20): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917119 | ||||||
chr4:98917121
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+11958_18+11973d others(18): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917121 | ||||||
chr4:98917123
|
CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0171a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG01261.hp1 HG01517.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+11960_18+11971d others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917123 | ||||||
chr4:98917123
|
CACACACA others(7): Show |
C | 6 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0067others(3): Show | 6 | HG02602.hp1 HG02738.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+11958_18+11971d others(16): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917123 | ||||||
chr4:98917125
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.18+11960_18+11969d others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917125 | ||||||
chr4:98917125
|
CACACACA others(5): Show |
C | 12 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0148others(9): Show | 12 | HG01070.hp2 HG03041.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+11958_18+11969d others(14): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917125 | ||||||
chr4:98917127
|
CACACACA others(3): Show |
C | 23 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0073others(20): Show | 23 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.18+11958_18+11967d others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917127 | ||||||
chr4:98917129
|
CACACAAA others(1): Show |
C | 26 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(23): Show | 26 | HG00558.hp2 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+11958_18+11965d others(10): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917129 | ||||||
chr4:98917131
|
CACAA | C | 19 | a0001c0001t0001g0010a0001c0001t0001g0207a0001c0001t0001g0215others(16): Show | 20 | HG00438.hp2 HG01934.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.18+11960_18+11963d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917131 | ||||||
chr4:98917131
|
CACAAAA | C | 37 | a0001c0001t0001g0058a0001c0001t0001g0096a0001c0001t0001g0104others(34): Show | 50 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.18+11958_18+11963d others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917131 | ||||||
chr4:98917133
|
C | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0253 | 3 | HG02258.hp2 NA18953.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.18+11962G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917133 | ||||||
chr4:98917133
|
CAA | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0092others(31): Show | 35 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.18+11960_18+11961d others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917133 | ||||||
chr4:98917133
|
CAAAA | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0093others(17): Show | 22 | HG01346.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.18+11958_18+11961d others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917133 | ||||||
chr4:98917135
|
A | C | 27 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0097others(24): Show | 27 | HG00673.hp1 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+11960T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917135 | ||||||
chr4:98917136
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0255 | 2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.18+11959T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917136 | ||||||
chr4:98917137
|
A | C | 39 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0057others(36): Show | 40 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.18+11958T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917137 | ||||||
chr4:98917138
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+11957T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917138 | ||||||
chr4:98917139
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.18+11956T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917139 | ||||||
chr4:98917279
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+11816T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917279 | ||||||
chr4:98917363
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.18+11732T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917363 | ||||||
chr4:98917680
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+11415C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917680 | ||||||
chr4:98917729
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.18+11366G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98917729 | ||||||
chr4:98918007
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.18+11088G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918007 | ||||||
chr4:98918071
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+11024T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918071 | ||||||
chr4:98918360
|
G | GA | 13 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(10): Show | 13 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.18+10734dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918360 | ||||||
chr4:98918409
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0232 | 2 | NA18953.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.18+10686A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918409 | ||||||
chr4:98918502
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+10593A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918502 | ||||||
chr4:98918536
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+10559C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918536 | ||||||
chr4:98918639
|
A | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 77 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.18+10456T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918639 | ||||||
chr4:98918648
|
A | T | 1 | a0001c0002t0003g0082 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.18+10447T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918648 | ||||||
chr4:98918652
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+10443A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918652 | ||||||
chr4:98918918
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.18+10177G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918918 | ||||||
chr4:98918938
|
A | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+10157T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918938 | ||||||
chr4:98918954
|
T | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+10141A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98918954 | ||||||
chr4:98919069
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.18+10026C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919069 | ||||||
chr4:98919071
|
G | T | 1 | a0001c0002t0003g0081 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.18+10024C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919071 | ||||||
chr4:98919122
|
C | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0119a0001c0001t0001g0120others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.18+9973G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919122 | ||||||
chr4:98919162
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+9933A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919162 | ||||||
chr4:98919175
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(71): Show | 77 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.18+9920G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919175 | ||||||
chr4:98919332
|
C | CA | 25 | a0001c0001t0001g0055a0001c0001t0001g0206a0001c0001t0001g0233others(22): Show | 26 | HG00621.hp1 HG00673.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+9762dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919332 | ||||||
chr4:98919332
|
CAA | C | 25 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(22): Show | 25 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+9761_18+9762del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919332 | ||||||
chr4:98919337
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.18+9748_18+9757del others(10): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919337 | ||||||
chr4:98919342
|
A | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 76 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+9753T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919342 | ||||||
chr4:98919345
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+9750T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919345 | ||||||
chr4:98919429
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+9666C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919429 | ||||||
chr4:98919452
|
C | T | 1 | a0001c0002t0003g0082 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.18+9643G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919452 | ||||||
chr4:98919485
|
T | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+9610A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919485 | ||||||
chr4:98919501
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0074 | 2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.18+9594T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919501 | ||||||
chr4:98919558
|
C | CT | 14 | a0001c0001t0001g0090a0001c0001t0001g0170a0001c0001t0001g0207others(11): Show | 14 | HG01243.hp1 HG02027.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.18+9536dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919558 | ||||||
chr4:98919558
|
CT | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0113others(4): Show | 7 | HG01123.hp2 HG01168.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+9536delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919558 | ||||||
chr4:98919850
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+9245A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98919850 | ||||||
chr4:98920231
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.18+8864A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920231 | ||||||
chr4:98920403
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.18+8692G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920403 | ||||||
chr4:98920452
|
G | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+8643C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920452 | ||||||
chr4:98920460
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.18+8635T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920460 | ||||||
chr4:98920512
|
C | G | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.18+8583G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920512 | ||||||
chr4:98920608
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.18+8487T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920608 | ||||||
chr4:98920808
|
C | A | 1 | a0001c0002t0003g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.18+8287G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920808 | ||||||
chr4:98920840
|
C | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(63): Show | 80 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.18+8255G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98920840 | ||||||
chr4:98921028
|
C | G | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+8067G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921028 | ||||||
chr4:98921051
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+8044T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921051 | ||||||
chr4:98921055
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+8040A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921055 | ||||||
chr4:98921100
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+7995A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921100 | ||||||
chr4:98921185
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+7910T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921185 | ||||||
chr4:98921205
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+7890A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921205 | ||||||
chr4:98921378
|
TA | T | 18 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.18+7716delT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921378 | ||||||
chr4:98921416
|
T | C | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+7679A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921416 | ||||||
chr4:98921962
|
A | G | 64 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(61): Show | 78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.18+7133T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98921962 | ||||||
chr4:98922142
|
C | T | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+6953G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922142 | ||||||
chr4:98922310
|
C | A | 1 | a0001c0002t0003g0006 | 2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.18+6785G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922310 | ||||||
chr4:98922312
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0110 | 4 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+6783G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922312 | ||||||
chr4:98922326
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+6769C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922326 | ||||||
chr4:98922332
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.18+6763G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922332 | ||||||
chr4:98922333
|
G | A | 1 | a0001c0001t0005g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.18+6762C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922333 | ||||||
chr4:98922353
|
C | T | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG01081.hp2 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+6742G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922353 | ||||||
chr4:98922413
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.18+6682C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922413 | ||||||
chr4:98922463
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.18+6632C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922463 | ||||||
chr4:98922553
|
C | CA | 19 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0106others(16): Show | 19 | HG01123.hp2 HG01192.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.18+6541dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922553 | ||||||
chr4:98922568
|
A | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0167others(2): Show | 6 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+6527T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922568 | ||||||
chr4:98922713
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18+6382A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922713 | ||||||
chr4:98922753
|
T | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+6342A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922753 | ||||||
chr4:98922830
|
T | G | 15 | a0001c0002t0003g0006a0001c0002t0003g0076a0001c0002t0003g0077others(12): Show | 16 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+6265A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922830 | ||||||
chr4:98922850
|
C | CT | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 66 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+6244dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922850 | ||||||
chr4:98922850
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.18+6245G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922850 | ||||||
chr4:98922850
|
CT | C | 66 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0047others(63): Show | 80 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.18+6244delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922850 | ||||||
chr4:98922865
|
TGA | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0154others(2): Show | 5 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+6228_18+6229del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922865 | ||||||
chr4:98922868
|
G | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0154others(2): Show | 5 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+6227C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922868 | ||||||
chr4:98922869
|
A | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0154others(2): Show | 5 | HG00558.hp2 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+6226T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922869 | ||||||
chr4:98922931
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0115a0001c0001t0001g0167others(2): Show | 6 | HG02145.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+6164A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922931 | ||||||
chr4:98922997
|
G | A | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+6098C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98922997 | ||||||
chr4:98923094
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.18+6001C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923094 | ||||||
chr4:98923157
|
C | A | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+5938G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923157 | ||||||
chr4:98923204
|
C | CA | 39 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0058others(36): Show | 39 | HG01109.hp1 HG01123.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+5890dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923204 | ||||||
chr4:98923208
|
A | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0162 | 2 | NA18956.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.18+5887T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923208 | ||||||
chr4:98923283
|
G | GAC | 65 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(62): Show | 79 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+5810_18+5811dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923283 | ||||||
chr4:98923319
|
CT | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 70 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.18+5775delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923319 | ||||||
chr4:98923596
|
C | T | 3 | a0001c0002t0003g0076a0001c0002t0003g0077a0001c0002t0003g0084 | 3 | HG00733.hp2 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.18+5499G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923596 | ||||||
chr4:98923611
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.18+5484G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923611 | ||||||
chr4:98923683
|
T | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+5412A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923683 | ||||||
chr4:98923816
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+5279T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98923816 | ||||||
chr4:98924077
|
G | GT | 3 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0003t0001g0161 | 3 | HG02615.hp2 HG03516.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.18+5017dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924077 | ||||||
chr4:98924081
|
A | AT | 18 | a0001c0001t0001g0075a0001c0001t0001g0238a0001c0001t0003g0091others(15): Show | 19 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.18+5013dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924081 | ||||||
chr4:98924081
|
A | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(70): Show | 76 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+5014T>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924081 | ||||||
chr4:98924081
|
AT | A | 10 | a0001c0001t0001g0260a0001c0001t0002g0044a0001c0001t0004g0173others(7): Show | 10 | HG01168.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+5013delA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924081 | ||||||
chr4:98924156
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0073 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+4939G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924156 | ||||||
chr4:98924235
|
C | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+4860G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924235 | ||||||
chr4:98924270
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+4825C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924270 | ||||||
chr4:98924322
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+4773G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924322 | ||||||
chr4:98924428
|
G | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+4667C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924428 | ||||||
chr4:98924593
|
G | GT | 16 | a0001c0001t0003g0091a0001c0002t0003g0006a0001c0002t0003g0076others(13): Show | 17 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+4501dupA | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924593 | ||||||
chr4:98924594
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.18+4501A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924594 | ||||||
chr4:98924813
|
G | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(6): Show | 9 | HG02647.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+4282C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924813 | ||||||
chr4:98924847
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.18+4248C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924847 | ||||||
chr4:98924955
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.18+4140C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924955 | ||||||
chr4:98924964
|
C | T | 47 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(44): Show | 60 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.18+4131G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924964 | ||||||
chr4:98924965
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4130C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924965 | ||||||
chr4:98924981
|
G | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+4114C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98924981 | ||||||
chr4:98925023
|
T | G | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+4072A>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925023 | ||||||
chr4:98925169
|
A | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+3926T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925169 | ||||||
chr4:98925326
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.18+3769A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925326 | ||||||
chr4:98925420
|
G | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG01070.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+3675C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925420 | ||||||
chr4:98925527
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+3568T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925527 | ||||||
chr4:98925543
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+3552G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925543 | ||||||
chr4:98925618
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0107a0001c0001t0001g0110 | 4 | HG00733.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+3477T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925618 | ||||||
chr4:98925679
|
A | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+3416T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925679 | ||||||
chr4:98925793
|
T | C | 3 | a0001c0002t0003g0083a0001c0002t0003g0088a0001c0002t0003g0089 | 3 | HG01081.hp1 HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.18+3302A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925793 | ||||||
chr4:98925811
|
G | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+3284C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925811 | ||||||
chr4:98925921
|
T | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+3174A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925921 | ||||||
chr4:98925922
|
TGA | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+3171_18+3172del others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98925922 | ||||||
chr4:98926011
|
T | TAAAAATT others(321): Show |
1 | a0001c0001t0001g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+3083_18+3084ins others(328): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926011 | ||||||
chr4:98926089
|
C | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+3006G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926089 | ||||||
chr4:98926110
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.18+2985C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926110 | ||||||
chr4:98926172
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.18+2923G>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926172 | ||||||
chr4:98926630
|
A | C | 8 | a0001c0001t0004g0173a0001c0001t0004g0185a0001c0001t0004g0186others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+2465T>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926630 | ||||||
chr4:98926690
|
A | G | 1 | a0001c0002t0003g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.18+2405T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926690 | ||||||
chr4:98926725
|
C | T | 26 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(23): Show | 26 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.18+2370G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926725 | ||||||
chr4:98926801
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 69 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.18+2294C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926801 | ||||||
chr4:98926955
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02280.hp2 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.18+2140G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98926955 | ||||||
chr4:98927163
|
T | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+1932A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927163 | ||||||
chr4:98927288
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.18+1807C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927288 | ||||||
chr4:98927327
|
G | A | 4 | a0001c0001t0004g0185a0001c0001t0004g0186a0001c0001t0004g0187others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+1768C>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927327 | ||||||
chr4:98927472
|
ATGG | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(65): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.18+1620_18+1622del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927472 | ||||||
chr4:98927528
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0046others(61): Show | 78 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.18+1567G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927528 | ||||||
chr4:98927550
|
A | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.18+1545T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927550 | ||||||
chr4:98927600
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.18+1495T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927600 | ||||||
chr4:98927654
|
C | CA | 30 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0238others(27): Show | 30 | HG00438.hp2 HG01168.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+1440dupT | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
C | CAA | 14 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(11): Show | 14 | HG00423.hp2 HG00735.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+1439_18+1440dup others(2): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAA | C | 6 | a0001c0002t0003g0084a0001c0002t0003g0087a0001c0002t0003g0088others(3): Show | 6 | HG00733.hp2 HG01358.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+1438_18+1440del others(3): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAA | C | 18 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(15): Show | 18 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.18+1437_18+1440del others(4): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAAA | C | 17 | a0001c0001t0001g0075a0001c0001t0001g0174a0001c0001t0001g0175others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+1436_18+1440del others(5): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAAAA | C | 25 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(22): Show | 25 | HG01346.hp2 HG02074.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.18+1435_18+1440del others(6): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAAAAA | C | 106 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 123 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.18+1434_18+1440del others(7): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG01074.hp1 HG01261.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+1433_18+1440del others(8): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 6 | HG01081.hp2 HG01123.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+1429_18+1440del others(12): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927654
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0005g0199others(1): Show | 4 | HG01943.hp1 HG01975.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+1428_18+1440del others(13): Show |
EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927654 | ||||||
chr4:98927836
|
C | A | 6 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(3): Show | 6 | HG00423.hp2 HG02129.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+1259G>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98927836 | ||||||
chr4:98928143
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG04115.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.18+952A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928143 | ||||||
chr4:98928519
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+576G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928519 | ||||||
chr4:98928520
|
G | C | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+575C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928520 | ||||||
chr4:98928532
|
G | C | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+563C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928532 | ||||||
chr4:98928533
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+562G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928533 | ||||||
chr4:98928612
|
G | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+483C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928612 | ||||||
chr4:98928640
|
G | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+455C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928640 | ||||||
chr4:98928671
|
G | C | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+424C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928671 | ||||||
chr4:98928673
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+422A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928673 | ||||||
chr4:98928676
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+419G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928676 | ||||||
chr4:98928680
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+415A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928680 | ||||||
chr4:98928684
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+411A>T | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928684 | ||||||
chr4:98928694
|
G | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+401C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928694 | ||||||
chr4:98928703
|
G | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+392C>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928703 | ||||||
chr4:98928713
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+382G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928713 | ||||||
chr4:98928719
|
G | C | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+376C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928719 | ||||||
chr4:98928721
|
G | C | 1 | a0001c0001t0002g0101 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.18+374C>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928721 | ||||||
chr4:98928773
|
C | T | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG01081.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+322G>A | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928773 | ||||||
chr4:98928779
|
T | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 103 | HG00558.hp2 HG00733.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.18+316A>G | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928779 | ||||||
chr4:98928975
|
A | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 215 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.18+120T>C | EIF4E | ENSG00000151247.13 | transcript | ENST00000450253.7 | protein_coding | 1/6 | chr4 | 98928975 |