BANF1 and intellectual disability-sparse hair-brachydactyly syndrome: In addition, our group previously described a shared DNAm episignature in Coffrin–Siris and Nicolaides–Baraitser syndromes (NCBRS) [64], which are two phenotypically similar NDDs associated with mutations in subunits of the BAF chromatin remodeling complex (commonly referred to as BAFopathies).