Additional file 4 of Universal annotation of the human genome through integration of over a thousand epigenomic datasets

Additional file 4. Full-stack states enrichments with repeats, prioritized variants, common variants, structural variants, CTCF, PRC1-PRC2, GWAS catalog variants, sex chromosomes, fine-mapped variants, cancer-associated variants. Excel version of Additional File 1: Figure S28: Full stack states enrichments with RepeatMasker classes of repeats and CG content. Excel version of Additional File 1: Figure S37: Enrichment of all full-stack states for top 1% bases prioritized by variant prioritization scores. Excel version of Additional File 1: Figure S32: Full-stack states enrichments with structural variants. Excel version of Additional File 1: Figure S42: Full-stack states enrichments with variants from GNOMAD stratified by minor allele frequencies, common variants and CG dinucleotides. Excel version of Additional File 1: Figure S14: Full-stack states enrichments with CTCF associated chromatin states. Excel version of Additional File 1: Figure S17B: Neighborhood enrichments of full-stack states with binding sites of PRC1 and PRC2 complexes. Excel version of Additional File 1: Figure S16: Full-stack states enrichments with Polycomb Repressive protein complexes PRC1 and PRC2. Excel version of Additional File 1: Figure S43: Full-stack states enrichments with GWAS catalog variants and sex chromosomes. Excel version of Additional File 1: Figure S44: Full-stack states enrichment values for fine-mapped variants at phenotype associated loci. Excel version of Additional File 1: Figure S47: Full-stack states enrichments with cancer-associated somatic mutations in the non-coding genome.