Because four of 33, or 12% of neuHP overlapped with neurodevelopmental susceptibility genes (CNTN4, CHL1, DPP10, SORCS1), we then checked whether the entire set of 410 human-specific peaks is enriched for genes and loci conferring genetic risk for autism, intellectual disability, and related neurological disease with onset in early childhood. This evidence concerns the gene CNTN4 and Intellectual disability.