Additional file 3: of Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants

Table S1. Demographic information for heterogeneous ASD cases and age- and sex-matched neurotypical controls. Table S2. Number of probes removed and remaining for analysis following quality control. Table S3. List of overlapping DMRs for 16p11.2del. Table S4. List of overlapping DMRs for CHD8+/−. Table S5. List of samples extracted from GEO database and respective 16p11.2del and CHD8+/− signature scores for specificity analysis. All sample data are from blood and from individuals with known ages < 50 years old. Table S6. List of significant (q < 0.05, |Δβ| ≥ 5%) sites in 16p11.2del DNAm signature. Table S7. List of significant (q < 0.05, |Δβ| ≥ 5%) sites in CHD8+/− DNAm signature. Table S8. GO Biological Process enrichment terms following GREAT enrichment analysis of differentially methylated genes in 16p11.2del DNAm signature. Table S9. GO Biological Process enrichment terms following GREAT enrichment analysis of differentially methylated genes in CHD8+/− DNAm signature. (XLSX 156 kb)