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). The gene discussed is SCN1A; the disease is Meckel syndrome, type 1.