{{Rsnum
|rsid=3729639
|Gene=E2F4
|Chromosome=16
|position=67191598
|Orientation=plus
|GMAF=0.152
|Gene_s=EXOC3L,E2F4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 86.7 | 13.3 | 0.0
| HCB | 93.4 | 6.6 | 0.0
| JPT | 96.5 | 3.5 | 0.0
| YRI | 18.4 | 53.7 | 27.9
| ASW | 47.4 | 36.8 | 15.8
| CHB | 93.4 | 6.6 | 0.0
| CHD | 97.2 | 2.8 | 0.0
| GIH | 68.3 | 25.7 | 5.9
| LWK | 20.9 | 52.7 | 26.4
| MEX | 86.2 | 13.8 | 0.0
| MKK | 35.9 | 46.8 | 17.3
| TSI | 91.2 | 7.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21347282
|Trait=None
|Title=Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
|RiskAllele=T
|Pval=2E-11
|OR=0.0900
|ORtxt=[0.06-0.12] SD increase
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}