Barely Significant
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Recurrent somatic mutations in regulatory regions of human cancer genomes.

Nat Genet · 2015 · PMC4485503 · PMID 26053494

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highly significantno p-value reported
We focused our attention on the highly significant enrichment of mutations in sites of the CEBP transcription factors and screened known binding site motifs for those with significantly higher match scores in the mutant CEBP sites than in the reference sites.

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