To disentangle specific CAD associations, we intersected the combined HCASMC-based ATAC, H3K27ac and TCF21/AP-1 ChIP-seq data with the CARDIoGRAMplusC4D variants, resulting in 87 candidate variants (30 variants ex vivo; Supplementary Data 7). The gene discussed is JUN; the disease is coronary artery disorder.