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. 2023 Jul 27;55(8):1301–1310. doi: 10.1038/s41588-023-01446-3

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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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Extended Data Fig. 1 — Average somatic mutation frequencies computed in sliding 2.5 megabase (Mb) windows with a step size of 100 kb across chromosome 1 obtained from an analysis of 2,511 PCAWG samples across 25 common cancer types. Adeno, adenocarcinoma; TCC, transitional cell carcinoma; Osteo, osteosarcoma; CNS, central nervous system; GBM, glioblastoma multiforme; Medullo, medulloblastoma; SCC, squamous cell carcinoma; ChRCC, chromophobe renal cell carcinoma; RCC, renal cell carcinoma; HCC, hepatocellular carcinoma; BNHL, B cell non-Hodgkin lymphoma; CLL, chronic lymphoid leukemia; MPN, myeloproliferative neoplasm; Endo, endocrine.