Barely Significant
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Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networks.

Nat Genet · 2025 · PMC12513834 · PMID 40968290

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closest p · 1.0× alpha
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of marginal significanceP < 0.05actually significant
Finally, to assess whether genes identified by our scCRISPRi screens were enriched in T cell-related networks, we relaxed our calling threshold to include variant CRE:gene interactions of marginal significance ( P < 0.05).

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