TY - JOUR AB - We develop a Bayesian model (BayesRR-RC) that provides robust SNP-heritability estimation, an alternative to marker discovery, and accurate genomic prediction, taking 22 seconds per iteration to estimate 8.4 million SNP-effects and 78 SNP-heritability parameters in the UK Biobank. We find that only ≤10% of the genetic variation captured for height, body mass index, cardiovascular disease, and type 2 diabetes is attributable to proximal regulatory regions within 10kb upstream of genes, while 12-25% is attributed to coding regions, 32–44% to introns, and 22-28% to distal 10-500kb upstream regions. Up to 24% of all cis and coding regions of each chromosome are associated with each trait, with over 3,100 independent exonic and intronic regions and over 5,400 independent regulatory regions having ≥95% probability of contributing ≥0.001% to the genetic variance of these four traits. Our open-source software (GMRM) provides a scalable alternative to current approaches for biobank data. AU - Patxot, Marion AU - Trejo Banos, Daniel AU - Kousathanas, Athanasios AU - Orliac, Etienne J AU - Ojavee, Sven E AU - Moser, Gerhard AU - Sidorenko, Julia AU - Kutalik, Zoltan AU - Magi, Reedik AU - Visscher, Peter M AU - Ronnegard, Lars AU - Robinson, Matthew Richard ID - 8429 IS - 1 JF - Nature Communications TI - Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits VL - 12 ER -