Eigen is a spectral approach to the functional annotation of genetic variants in coding and noncoding regions. Eigen makes use of a variety of functional annotations in both coding and noncoding regio
a SNVs that were predicted by both dmax and rmin measures are highlighted with †. b The p-value corresponding to the rmin measure is highlighted with *. c The conserved RNA secondary structure predict
The location of transcribed and DHSP overlapping variants on chromosome 15 (hg19 build), with transcribed SNPs indicated with asterisks. SNP alleles (mA) identified exclusively on the risk haplotype a
