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. 2023 May 10;617(7960):325–334. doi: 10.1038/s41586-023-05895-y

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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 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/.

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Extended Data Fig. 7 — a) Density of IGC acceptor (top, blue) and donor (bottom, orange) sites across the “SD genome”. The SD genome consists of all main SD regions (>50 kbp) minus the intervening unique sequences. b) All intrachromosomal IGC events from 102 human haplotypes analyzed for chromosome 15. Arcs drawn in blue (top) have the acceptor site on the left-hand side and the donor site on the right. Arcs drawn in orange (bottom) are arranged oppositely. Protein-coding genes are drawn as vertical black lines above the ideogram, and large duplication (blue) and deletion (red) events associated with human diseases are drawn as horizontal lines just above the ideogram. c) Zoom of the 100 highest confidence (lowest p-value) IGC events identified on chromosome 15 between 17 and 31 Mbp. Genes that are intersected by IGC events are highlighted in red.