Fig. 2From: Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypesGenetic colocalization reveals shared regulatory loci and implicates causal genes underlying genetic associations between hematopoietic traits and disease end-points. a Number of traits identified at each colocalization site (max = 24). b Heat map depicting percent overlap at colocalization sites between each trait pair. In each box, the number of sites where the row-specified trait and column-specified trait colocalized was normalized to the total number of colocalization sites for the ‘row trait’. For this reason, the heat map is asymmetric. c Hierarchical clustering based on colocalization results associates related traits, which are color coded according to the key in part b. d Degree of colocalization (% overlap) reflects genetic correlation between trait pairs. Shaded area depicts the 95% prediction interval, with gray line at mean. Exemplary trait pairs are circled. Depsx, depressive symptoms. Rbc, red blood cell count. Baso, basophil cell count. Brca, breast cancer. Scz, schizophrenia. Eo%, eosinophil percentage of white blood cells (‘eo_p’) or granulocytes (‘eo_p_gran’)Back to article page