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. 2020 Oct 7;13:42. doi: 10.1186/s13072-020-00361-9

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© The Author(s) 2020

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. 7 — DMRs and H3K9me2 levels in leaf and flower samples. a Total number of CG, CHG, and CHH hyper-DMRs in flower and leaf samples. b Distribution of CG, CHG, and CHH hyper-DMRs in chromosomal arms and heterochromatins. c Enrichment of CG, CHG, and CHH hyper-DMRs in various regions relative to genes. Expected level (1, marked by dotted line) is estimated based on genomic distribution of randomly selected regions of equal size from Arabidopsis genome. d H3K9me2 levels in TEs from chromosomal arms (without flower hyper-CHG DMRs) and heterochromatins (with flower hyper-CHG DMRs)