Fig. 4

Scatterplot of SNVs in the 9p21.3 locus with Posterior Inclusion Probability (PIP) (y-axis) against Chromosome 9 Position (x-axis) for FINEMAP (A) and SuSie (B). The first credible set of both approaches include the same 13 SNVs which are highlighted with larger darker circles and annotated with rsIDs.