SNV associated_with Gm12878

Subject: SNV
Relation: associated_with
Object: Gm12878
p-value: —

Evidence from: primary | all sources

Evidence (1 sources)

Annotation of functional variation in personal genomes using RegulomeDB. (2012) PMID:22955989 cited

We annotated the SNVs of GM12878 from Complete Genomics with RegulomeDB

confidence: 0.95