SEA version 4.0: a major expansion and update of the Super-Enhancer Archive

Super-enhancers (SEs) are pivotal epigenetic regulatory elements that profoundly influence cell fate and disease. We herein present an updated SEA version 4.0, a systematic platform designed to elucidate the roles of SEs. A uniform computational pipeline was established to identify SEs based on five key histone marks, using H3K27ac, BRD4, p300, Med1, and the newly added H3K4me1, across 14 species. 496 071 SEs and 29 584 078 enhancers have been stored in the database. It provides extensive genome annotations, including nearby genes, transcription factor binding sites, chromatin accessibility, and other gene regulation signatures. SEA version 4.0 has also achieved functional enrichment analysis of SEs. And a Shannon entropy-based algorithm is employed to identify specific SEs. Furthermore, SEA version 4.0 introduces an interactive regulatory network that incorporates SEs, enhancers, transcription factors, and proximal genes for human and mouse. Additionally, a cell-specific SE detector is provided, designed for cancer research by leveraging scRNA-seq data from 12 cancer and normal samples to explore cell-type-specific SEs. The performance interaction and visualization of SEA version 4.0 enable genomic and cross-species comparisons, revealing complex genomic interactions and becoming an indispensable resource for decoding the mechanisms of SE in development and disease. Access freely at http://sea4.edbc.org.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-10-31
DOI
https://doi.org/10.1093/nar/gkaf1114
Primary Topic
Genomics and Chromatin Dynamics
Type
article
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article

SEA version 4.0: a major expansion and update of the Super-Enhancer Archive

Li Yu, Ruiyang Zhai, Chenye Zhang, Tao Feng et al.
Nucleic Acids Research
Genomics and Chromatin Dynamics
article

SEA version 4.0: a major expansion and update of the Super-Enhancer Archive

Li Yu, Ruiyang Zhai, Chenye Zhang, Tao Feng, Yue Gu, Jiyun Zhao, Yan Zhang, Bowen Shi, Li Deng, Chao Ji, Hongli Wang
article en

Abstract

Super-enhancers (SEs) are pivotal epigenetic regulatory elements that profoundly influence cell fate and disease. We herein present an updated SEA version 4.0, a systematic platform designed to elucidate the roles of SEs. A uniform computational pipeline was established to identify SEs based on five key histone marks, using H3K27ac, BRD4, p300, Med1, and the newly added H3K4me1, across 14 species. 496 071 SEs and 29 584 078 enhancers have been stored in the database. It provides extensive genome annotations, including nearby genes, transcription factor binding sites, chromatin accessibility, and other gene regulation signatures. SEA version 4.0 has also achieved functional enrichment analysis of SEs. And a Shannon entropy-based algorithm is employed to identify specific SEs. Furthermore, SEA version 4.0 introduces an interactive regulatory network that incorporates SEs, enhancers, transcription factors, and proximal genes for human and mouse. Additionally, a cell-specific SE detector is provided, designed for cancer research by leveraging scRNA-seq data from 12 cancer and normal samples to explore cell-type-specific SEs. The performance interaction and visualization of SEA version 4.0 enable genomic and cross-species comparisons, revealing complex genomic interactions and becoming an indispensable resource for decoding the mechanisms of SE in development and disease. Access freely at http://sea4.edbc.org.

Nucleic Acids ResearchVol. 54(D1)
Harbin Medical University (CN), Harbin Institute of Technology (CN), Fourth Affiliated Hospital of Harbin Medical University (CN), Qiqihar Medical University (CN)
Openalex Percentile: Top 72%
Genomics and Chromatin Dynamics
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