In this analysis, significant H3K27ac signal at MAGI2 introns and the coding region was found of in-house patient-derived MM tissues (MM 1–10), also in another independent MM dataset (MM 11–13), and HMCLs (JJN3 and MM1.S), but not in the control samples (Fig. 4D). The gene discussed is MAGI2; the disease is Miyoshi myopathy.