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. 2021 Feb 26;12:1344. doi: 10.1038/s41467-021-21536-2

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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. 5 — a Flow cytometry plot of G₁ stage FUCCI B cells that were flow cytometry purified by monomeric Kusabira Orange 2 (mKO2) and monomeric Azami Green (mAG) expression just prior to the first division (33 h). b Multidimensional-scaling plot of the filtered and normalized logCPM values for interacting promoters during B-cell activation with Pre-S samples included. c Bar plot showing the number of differentially interacting promoters (DIPs) between each transition of B-cell activation with Pre-S samples included. Blue indicates decreased promoter interactions. Red indicates increased promoter interactions. Source data are provided as a Source Data file.