Comprehensive multi-omics integration identifies differentially active enhancers during human brain development with clinical relevance.

Genome Med · 2021 · PMC8524963 · PMID 34663447

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nominally significantno p-value reported

They found an enrichment of rare non-coding CNVs near known epilepsy genes, with the GABRD gene showing the strongest and only nominally significant association with 4 non-coding deletions amongst the epilepsy patients.

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