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. 2024 Jan 10;15:433. doi: 10.1038/s41467-023-44467-6

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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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Fig. 1 — In an overlapping set of kidney samples, tissue was interrogated by laser microdissection-guided whole genome bisulfite sequencing (WGBS), by multiome single nucleus Assay for Transposase-Accessible Chromatin for sequencing (snATAC-seq) and single nucleus RNA sequencing (snRNAseq) after cell disaggregation, and by Cleavage Under Targets & Release Using Nuclease (CUT&RUN) of kidney cortex. Datasets were aligned in the human genome 38 to create an integrated epigenomic atlas.