Recently, we have identified eight variants in linkage disequilibrium with the reported CELF1/rs10838725 that have suggestive functional relevance (RegulomeDB score: 1f) and are eQTLs for C1QTNF4. These data suggest that CELF1 may be acting in conjunction with or serving as a proxy for other genes in this region that mediate AD risk [Rosenthal, unpublished data]. The gene discussed is CELF1; the disease is Alzheimer disease.