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 KCNH5; the disease is nervous system disorder.