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. 2021 Aug 11;13:157. doi: 10.1186/s13148-021-01145-y

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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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