Description:

The eQTL Fine-Mapping module collects the 90% credible sets of potential causal variants for eQTLs in each gene across 25 types of human cancers. You can search fine-mapping results by selecting a cancer type and a gene name or entering an SNP ID. The result table displays the 90% credible sets for each gene and the PIP value for each SNP. You can click the 'Plot' button to generate a locus plot displaying the PIP values of all SNPs in the cis-region of the target gene.