Mapping common regulatory variants to human haplotypes

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Abstract

Inter-individual variation in gene expression has proven to be in part governed by genetic determinants, which may be trans- or cis-acting. The underlying cause of cis-acting regulatory variation has been identified in only a handful of the hundreds of genes shown to display differential allelic expression. In this report, we describe a systematic effort to map common cis-acting variants in 64 genes, using association methods in HapMap samples. We identified 16 loci (25%), each of which harbors common haplotypes that affect total expression of a gene, and a further 17 loci (27%) with evidence of haplotypes affecting relative allelic expression in heterozygote samples. Our survey suggests that detailed mapping of allele-specific in vivo expression will provide a rich source of regulatory SNPs or haplotypes that should be given high priority in association studies of human phenotypes. © The Author 2005. Published by Oxford University Press. All rights reserved.

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Pastinen, T., Ge, B., Gurd, S., Gaudin, T., Dore, C., Lemire, M., … Hudson, T. J. (2005). Mapping common regulatory variants to human haplotypes. Human Molecular Genetics, 14(24), 3963–3971. https://doi.org/10.1093/hmg/ddi420

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