The top candidates include TNFAIP3, which has been reported before, but also include other, novel regions, containing genes involved in blood diseases (CYCS), neurological diseases (PRKCH, KCNH5, LRNN1), metabolism (SFRP4, SUMF1), and skin development (ASCL4, RAB27A). The gene discussed is TNFAIP3; the disease is blood disease.