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. 2024 Nov 21;56(12):2646–2658. doi: 10.1038/s41588-024-01952-y

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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. 4 — a, Fine-mapped variants at genomic risk loci with variants with high CADD Phred scores (>20) annotated to the nearest gene. b, Total number and function of fine-mapped variants at each locus. c, Distribution of CADD Phred scores for fine-mapped variants across all genomic risk loci, stratified by variant function. d, Number of fine-mapped variants stratified by function.