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. 2021 Aug 30;4:1016. doi: 10.1038/s42003-021-02556-6

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© The Author(s) 2021

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. 6 — a Venn diagram of alignment of CPG to three human genomes, HX1 (Chinese), KOREF1.0 (Korean), and NA18507 (African). The alignments were based on at least 90% identity. b The length distribution of novel sequences from APG and CPG that can be aligned with each other with ≥90% identity. CPG2APG: CPG aligned to APG. APG2CPG: APG aligned to CPG. c The length distribution of novel sequences from CPG and HCPG that can be aligned with each other with ≥90% identity. CPG2HCPG: CPG aligned to HCPG. HCPG2CPG: HCPG aligned to CPG.