Extended Data Fig. 4: Distribution of annotations of lead rare pQTL non-coding non-cognate variants compared to all variants tested.

Proportion of variants in sets of lead variants (N = 261; dark blue) compared to all variants tested (N = 35,120,659 light blue), if the variant was not annotated to the cognate gene. 95% confidence intervals of proportions shown by whiskers. p-values are derived from a two-sided Fisher’s exact test. Text in bolded red indicates a comparison with evidence of enrichment or depletion at P < 0.05/9.