Fig. 3
Bayesian risk variant inference for SNPs within the RBSG4 and the MIR486/NKX6.3 loci. Panel (a) corresponds to RBSG4 (LINC01363) and panel (b) to MIR486/NKX6.3. Tracks from top to bottom display: (1) gene track, (2) −log10 association p-values from the meta-analysis, (3) posterior probability of disease association (PPA), (4) the number of overlapping epigenomic annotation at a given marker, (5) the detail of the epigenomic marks that overlap a given variant. The risk inference analyses are limited to variants with p-values smaller than 10−3; all other variants are not displayed. Due to a large number of DNase annotation tracks (>100 for specific variants), these tracks have been reduced to a single one (referred as “DNase”). Source data are provided as a Source Data file
