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. 2021 Dec 22;21:701. doi: 10.1186/s12935-021-02413-w

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© The Author(s) 2021

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 5 — Mutant and transcriptional regulation analysis of SMARCC1 in HCC. a The schematic representation of SMARCC1 mutations in HCC. b, c The mutation types of SMARCC1 (%) in HCC. d Transcription factors with high regulatory potential in HepG2 cell lines from Cistrome DB database (10 k distance to TSS). e The prognostic values of ZBTB40 in HCC from Kaplan‐Meier Plotter online tool. f The relevance of SMARCC1 expression in relation to ZBTB40 expression in HCC from GEPIA database. g Relationships of SMARCC1 with DNA methylation in HCC based on TCGA database