SCNM1 and Meckel syndrome, type 1: In total, 15 genes were detected to harbor MEs among the epilepsy-associated genes, and genes which are more frequent to harbor MEs in TLE include BRD2, DOCK7, HERC2, IGSF8, NF1, NIN, PCLO, RFX3, SCN1A, SCNM1, and TBCK (Supplementary Table S4).