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. 2023 Mar 15;616(7955):113–122. doi: 10.1038/s41586-023-05795-1

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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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Fig. 5 — a, Brightfield image, spatial distribution and UMAP of all clusters based on ATAC and RNA in the human hippocampus. ML, molecular layer; Pyr, pyramidal neurons. Pixel size, 50 μm, scale bars, 1 mm. b, Integration of our ATAC data with scATAC-seq data⁴² from human hippocampus. c, Integration of our RNA data with snRNA-seq data from human brain⁴³. d, Spatial mapping of GAS and gene expression for selected marker genes in different clusters for ATAC and RNA. Oligo, oligodendrocytes; astro, astrocytes; DG, dentate gyrus.