Variants in the three-way intersections of credible sets predicetd to alter chromatin accessibility in brain cell types.
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The columns contain:– cell_type: as in [32]– coordinates: SNP coordinates, hg38– rsid: SNP id– ref: reference allele– alt: alternate allele– delta_svm: deltaSVM value– ENSG00000267801, ENSG00000178952, ENSG00000237742, ENSG00000160695: whether the SNP is included in the three-way intersection of credible sets for each gene – cell_type: as in [32] – coordinates: SNP coordinates, hg38 – rsid: SNP id – ref: reference allele – alt: alternate allele – delta_svm: deltaSVM value – ENSG00000267801, ENSG00000178952, ENSG00000237742, ENSG00000160695: whether the SNP is included in the three-way intersection of credible sets for each gene (XLSX)
创建时间：
2025-04-10
