nominally significantp < 0.0001
We performed colocalization analyses for each of the identified loci with an nominally significant eQTL ( p < 0.0001) and assumed a single causal variant within the window tested (lead eQTL SNP +/− 200KB).
We performed colocalization analyses for each of the identified loci with an nominally significant eQTL ( p < 0.0001) and assumed a single causal variant within the window tested (lead eQTL SNP +/− 200KB).