Individual probes were screened to assess if the strong cis-effects are due to hybridization artifacts caused by SNPs in probe targets. Thirteen candidate genes with cis-QTLs were then selected for further analysis and validation of cis-regulation by measuring allele specific expression (ASE) difference [56]. This method exploits transcribed SNPs, and uses single base extension to assess expression difference in F1 hybrids. By means of ASE, we validated the cis-regulation of 10 candidate genes—Ndufs2, Nit1, Pfdn2, Usf1, Copa, Atp1a2, Kcnj9, Kcnj10, Dfy, and Fmn2 (table 4). Adamts4 and Igsf4b failed to show significant allelic expression difference. In the case of Ufc1, the polarity of the allele effect failed to agree with the ASE result (D positive at p-value = 0.02).
