We screened all Affymetrix probe sets with cis-QTLs in Qrr1 for SNPs in target sequences. This step was taken to identity false cis-QTLs caused by differences in hybridization. As probe design is based on the B6 sequence, such spurious cis-QTLs show high expression for the B allele, and low expression for the D allele. Our screening identified only two probe sets in which SNPs result in spurious local QTLs—1429382_at (Tomm40l), and 1452308_a_at (Atp1a2). The majority of cis-QTLs in Qrr1 are likely to be due to actual differences in mRNA abundance. We did not detect a bias in favor of the B allele on cis-regulated expression and the ratio of transcripts with B- and D- positive additive effects is close to 1∶1.
