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. 2021 Jun 18;12:3797. doi: 10.1038/s41467-021-23824-3

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© The Author(s) 2021

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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Fig. 4 — ATAC-seq and ChIP-seq data from all mature OSNs^21,27 in genomic regions corresponding to TE1 and TE2, and known functional OR enhancers: H, P, A (J core), Lipsi, Sfaktiria and Kefallonia. T-elements show similar chromatin accessibility, but lack Lhx2, Ebf1 (O/E), and Ldb1 binding that is observed in most of the known functional OR enhancers.