We also identified potentially novel, strong cis-eQTLs for SNF8 and ATP5G1 at the UBE2Z locus, and OAS2 at the SH2B3 locus where the CAD/MI GWAS risk SNP was in very strong LD with our lead eQTL (Additional file 1: Table S12). The gene discussed is SNF8; the disease is coronary artery disorder.