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). This evidence concerns the gene RAB27A and nervous system disorder.