Linking disease associations with regulatory information in the human genome.

Genome Res · 2012 · PMC3431491 · PMID 22955986

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barely significantno p-value reported

At an r 2 LD threshold of 0.8, enrichments for most individual modalities are barely significant, but enrichment for functional SNPs supported by multiple sources of evidence remains significant (Supplemental Tables 3, 4).

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.