Barely Significant
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Chromatin accessibility variation provides insights into missing regulation underlying immune-mediated diseases.

Elife · 2025 · PMC12705069 · PMID 41396161

Europe PMCDOI
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hedged sentence
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closest p · 1.0× alpha
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nominally significantp<0.05actually significant
Interestingly, SCZ showed a nominally significant proportion of caQTL-mediated heritability in LCLs (p<0.05, MESC), consistent with the hypothesis that B cells may play some role in SCZ pathogenesis ( Schizophrenia Working Group of the Psychiatric Genomics Consortium, 2014 ; van Mierlo et al., 2019 ).

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