Stroke-associated intergenic variants modulate a human FOXF2 transcriptional enhancer.

Proc Natl Acad Sci U S A · 2022 · PMC9436329 · PMID 35994645

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highly significantno p-value reported

Discussion Despite the large number of GWASs identifying highly significant disease-associated loci, correlation between GWAS-identified SNPs and a biological function has been a major barrier in implementing the findings, particularly when variants are located in intergenic regions.

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