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. 2024 Jul 11;632(8026):832–840. doi: 10.1038/s41586-024-07773-7

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© The Author(s) 2024

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. 5 — Median proportion of possible SNVs observed in UK Biobank per 18 bp window across 1,000 intergenic regions on chromosome 12 (grey) and RNU4-1, RNU4-2 (teal). A median of 76% of all possible SNVs in RNU4-2 are observed compared with 13% on average in the intergenic sequences of the same length (141 bp; P < 0.001, Monte Carlo Fisher-Pitman test).

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