Fig. 1: Examples of the enrichment of variant–gene pairs in whole-blood eQTL PIP bins for functional genomics features. | Nature Communications

Fig. 1: Examples of the enrichment of variant–gene pairs in whole-blood eQTL PIP bins for functional genomics features.

From: Leveraging supervised learning for functionally informed fine-mapping of cis-eQTLs identifies an additional 20,913 putative causal eQTLs

Fig. 1

Enrichments of variant–gene pairs in different posterior inclusion probability (PIP) bins in binary functional features (non-tissue specific (a), tissue-specific in peripheral blood mononuclear cells (b), deep learning-derived regulatory activity (CAGE46) prediction in neutrophils (c), and distance to TSS (d) are shown (n is the number of variant–gene pairs).

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