Discovery of genome-wide association studies (GWAS) variants in different genomic elements and disease types. GWAS variants were assigned to a disease type (y axis) or non-disease traits. For each disease type, the P-value (x axis) for a skew towards a particular genomic category (x xis) was calculated (see Additional file 1: Supplementary Text). Numbers of unique GWAS variants for each of the genomic categories are shown as the purple bars; the corresponding numbers for each of the disease types are shown in parenthesis. Only disease types with >100 GWAS variants are shown. CDS, coding DNA sequence (coding regions of known genes); UTR, untranslated region (non-coding regions of known genes; promoter and intronic regions are those of known genes). See Additional file 1: Supplementary Text for details of the analysis.
St. Laurent et al. BMC Medicine 2014 12:97 doi:10.1186/1741-7015-12-97