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Fig. 4 | Clinical Epigenetics

Fig. 4

From: Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile

Fig. 4

DYT28 is characterized by a hypermethylation pattern on specific gene regions. Histograms illustrate the non-random gene region distribution for episignature’s probes (A), and DMRs (B) in DYT28 patients. Fisher’s exact test was used to report the statistical significance of the enrichment/depletion with respect to genomic background (EPIC array). TSS200, transcription start sites 1–200; TSS, transcription start sites 201–1500; IGR, intergenic regions. A Percentage and statistical significance of feature enrichment for DYT28 episignature: *P < 0.01; **P < 10−3 ***P < 10−6; B Percentage and statistical significance of feature enrichment for DMRs in DYT28 patients: *P < 0.05; **P < 0.01 ***P < 0.001

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