Breast cancer risk–associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression

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Integrative functional genomics identifies an enhancer looping to the SOX9 gene disrupted by the 17q24.3 prostate cancer risk locus

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Epigenomic Enhancer Profiling Defines a Signature of Colon Cancer

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Polymorphisms in the TOX3/LOC643714 Locus and Risk of Breast Cancer in African-American Women

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TOX3 is a neuronal survival factor that induces transcription depending on the presence of CITED1 or phosphorylated CREB in the transcriptionally active complex

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Upregulation of c-MYC in cis through a Large Chromatin Loop Linked to a Cancer Risk-Associated Single-Nucleotide Polymorphism in Colorectal Cancer Cells

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A map of open chromatin in human pancreatic islets

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

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FOXA1 is a key determinant of estrogen receptor function and endocrine response

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Identification of a Functional Genetic Variant at 16q12.1 for Breast Cancer Risk: Results from the Asia Breast Cancer Consortium

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Androgen Receptor Regulates a Distinct Transcription Program in Androgen-Independent Prostate Cancer

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Histone modifications at human enhancers reflect global cell-type-specific gene expression

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The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer

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The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling

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Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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FoxA1 Translates Epigenetic Signatures into Enhancer-Driven Lineage-Specific Transcription

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Microarray Technology and Applications in the Arena of Genome-Wide Association

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Unique ERα Cistromes Control Cell Type-Specific Gene Regulation

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Model-based Analysis of ChIP-Seq (MACS)

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