First, the genomic segment on human chromosome 15q26 containing NR2F2 was 1 of 6 moderately associated regions for hypertension identified by the Wellcome Trust Case Control Consortium88 Second, a reanalysis of the Wellcome Trust Case Control Consortium data by haplotypic analysis points to a CAA haplotype within the human NR2F2 gene as the only region that is associated with very high significance to hypertension.89 Here, NR2F2 is linked to hypertensive disorder.