Annotation of functional variation in personal genomes using RegulomeDB

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 3.
Figure 3.

Protein coding and noncoding SNVs can be classified as potentially functional by Polyphen-2 and RegulomeDB, respectively. Heterozygous, damaging coding SNVs can act in conjunction with a heterozygous regulatory SNV on the opposite allele to create a compound heterozygote and loss of function on both alleles (one regulatory, the other coding).

This Article

  1. Genome Res. 22: 1790-1797

Preprint Server