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. 2022 Oct 7;11(1):60. doi: 10.1038/s41389-022-00435-1

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© The Author(s) 2022

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 — A Doughnut chart showing the percentage distribution of ZNF148 chromatin occupancy peak locations determined by BioChIP-seq. B Consensus DNA binding motif analysis of ZNF148 occupied sequences (HOMER) [43]. The top 5 representative DNA binding sequence motifs were ranked by p-value and known transcription factors. C Representative BioChIP-seq signals at the bone morphogenetic protein 4 (BMP4) locus in MDA-MB-231 cells expressing BirA alone or BirA and FB-ZNF148. D As in “C” for SMAD family member 6 (SMAD6) locus. E As in “C” for discoidin domain receptor tyrosine kinase 1 (DDR1) locus. F GO biological process analysis of ZNF148 top 1500 peaks. G GO cellular component analysis of ZNF148 top 1500 peaks.