Table_S8_PPC_CandidateCausalVariants_PP0.01.robj

For each significant iPSC-PPC egQTL and eiQTL, we provide all fine-mapped SNPs with PP >= 1%. Missing eQTLs in this table are due to not having SNPs above the threshold. Specifically, we provide: the eQTL phenotype (gene expression or isoform usage); transcript ID; gene ID; eQTL discovery order (0 represents primary eQTL; 1-4 represents conditional eQTLs with 1 being the first conditional and 4 being the fourth conditional); eQTL ID (first term corresponds to the discovery order and the second term corresponds to the transcript ID); SNP ID; fine-mapping statistics from COLOC (Giambartolomei et al., 2014); and posterior probability (PP) for the SNP (“SNP.PP”).