An expanded registry of candidate cis-regulatory elements

J. Russell Moore(UMass Memorial Health Care), Henry E. Pratt(University of Massachusetts Chan Medical School), Kaili Fan(University of Massachusetts Chan Medical School), Nishigandha Phalke(University of Massachusetts Chan Medical School), Jonathan A. D. Fisher(University of Massachusetts Chan Medical School), Shaimae I. Elhajjajy(University of Massachusetts Chan Medical School), Gregory Andrews(University of Massachusetts Chan Medical School), Mingshi Gao(University of Massachusetts Chan Medical School), Nicole Shedd(University of Massachusetts Chan Medical School), Y. Fu(University of Massachusetts Chan Medical School), Matthew C Lacadie(University of Massachusetts Chan Medical School), Jair Meza(University of Massachusetts Chan Medical School), Mansi Khandpekar(University of Massachusetts Chan Medical School), Mohit Ganna(University of Massachusetts Chan Medical School), Eva Choudhury(University of Massachusetts Chan Medical School), Ross Swofford(University of Massachusetts Chan Medical School), Huong Phan(University of Massachusetts Chan Medical School), C. J. Ramírez(University of Massachusetts Chan Medical School), Maxwell Campbell(University of Massachusetts Chan Medical School), Mary E. Likhite(University of Massachusetts Chan Medical School), Nina Farrell(Broad Institute), Annika K. Weimer(Stanford University), Anusri Pampari(Stanford University), Vivekanandan Ramalingam(Stanford University), Fairlie Reese(University of California, Irvine), Beatrice Borsari(Yale University), Xuezhu Yu(Yale University), Eve S. Wattenberg(Yale University), Marina Ruiz-Romero(Centre for Genomic Regulation), Milad Razavi-Mohseni(Johns Hopkins University), Jinrui Xu(Howard University), Timur R. Galeev(Yale University), Andrés Colubri(Broad Institute), M Beer(Johns Hopkins University), Roderic Guigó(Universitat Pompeu Fabra), M. Gerstein(Yale University), J Engreitz(Broad Institute), Mats Ljungman(University of Michigan), Timothy E. Reddy(Duke University), Michael P. Snyder(Stanford University), Charles B. Epstein(Broad Institute), Elizabeth Gaskell(Broad Institute), B Bernstein(Broad Institute), Diane E. Dickel(Lawrence Berkeley National Laboratory), Axel Visel(Lawrence Berkeley National Laboratory), L Pennacchio(Lawrence Berkeley National Laboratory), Ali Mortazavi(University of California, Irvine), Anshul Kundaje(Stanford University), Zhiping Weng(UMass Memorial Health Care)
Nature
January 7, 2026
Cited by 19Open Access
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Abstract

Abstract Mammalian genomes contain millions of regulatory elements that control the complex patterns of gene expression 1 . Previously, the ENCODE consortium mapped biochemical signals across hundreds of cell types and tissues and integrated these data to develop a registry containing 0.9 million human and 300,000 mouse candidate cis -regulatory elements (cCREs) annotated with potential functions 2 . Here we have expanded the registry to include 2.37 million human and 967,000 mouse cCREs, leveraging new ENCODE datasets and enhanced computational methods. This expanded registry covers hundreds of unique cell and tissue types, providing a comprehensive understanding of gene regulation. Functional characterization data from assays such as STARR-seq 3 , massively parallel reporter assay 4 , CRISPR perturbation 5,6 and transgenic mouse assays 7 have profiled more than 90% of human cCREs, revealing complex regulatory functions. We identified thousands of novel silencer cCREs and demonstrated their dual enhancer and silencer roles in different cellular contexts. Integrating the registry with other ENCODE annotations facilitates genetic variation interpretation and trait-associated gene identification, exemplified by the identification of KLF1 as a novel causal gene for red blood cell traits. This expanded registry is a valuable resource for studying the regulatory genome and its impact on health and disease.


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