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. 2023 Oct 30;55(11):1912–1919. doi: 10.1038/s41588-023-01553-1

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© The Author(s) 2023

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — a, Fraction of females (n = 41,895 biologically independent individuals) and males (n = 25,495 biologically independent individuals) with one or more autosomal mCA across age bins. Error bars represent 95% confidence intervals. b, Fraction of individuals across different genetic ancestry groups with one or more autosomal mCA across age bins. c, Fraction of females (n = 41,895 biologically independent individuals) with a chrX mCA across age bins. Error bars represent 95% confidence intervals. The inset shows a histogram of chrX mCA calls. The X axis shows 1 Mb windows across chrX, and the Y axis is the number of mCA calls that span the genomic window. d, Fraction of females across different genetic ancestry groups with a chrX mCA across age bins.