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Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants

https://doi.org/10.1073/pnas.1317023110
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Position-independent, high-level expression of the human β-globin gene in transgenic mice
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Five Years of GWAS Discovery
inferredcites →https://doi.org/10.1016/j.ceb.2013.02.003openalex-snapshot
Cohesin at active genes: a unifying theme for cohesin and gene expression from model organisms to humans
inferredcites →https://doi.org/10.1016/j.cell.2006.02.041openalex-snapshot
A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/j.cell.2011.12.014openalex-snapshot
Extensive Promoter-Centered Chromatin Interactions Provide a Topological Basis for Transcription Regulation
inferredcites →https://doi.org/10.1016/j.cell.2012.12.033openalex-snapshot
Genome-wide Chromatin State Transitions Associated with Developmental and Environmental Cues
inferredcites →https://doi.org/10.1016/j.cell.2013.03.035openalex-snapshot
Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes
inferredcites →https://doi.org/10.1016/j.cell.2013.03.036openalex-snapshot
Selective Inhibition of Tumor Oncogenes by Disruption of Super-Enhancers
inferredcites →https://doi.org/10.1016/j.cell.2013.07.034openalex-snapshot
Transcription Factor Binding in Human Cells Occurs in Dense Clusters Formed around Cohesin Anchor Sites
inferredcites →https://doi.org/10.1016/j.cmet.2010.09.012openalex-snapshot
Global Epigenomic Analysis of Primary Human Pancreatic Islets Provides Insights into Type 2 Diabetes Susceptibility Loci
inferredcites →https://doi.org/10.1038/nature09266openalex-snapshot
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
inferredcites →https://doi.org/10.1038/nature09906openalex-snapshot
Mapping and analysis of chromatin state dynamics in nine human cell types
inferredcites →https://doi.org/10.1038/nature11247openalex-snapshot
An integrated encyclopedia of DNA elements in the human genome
inferredcites →https://doi.org/10.1038/nature11279openalex-snapshot
The long-range interaction landscape of gene promoters
inferredcites →https://doi.org/10.1038/nbt.1662openalex-snapshot
Discovery and characterization of chromatin states for systematic annotation of the human genome
inferredcites →https://doi.org/10.1038/nbt.2422openalex-snapshot
Interpreting noncoding genetic variation in complex traits and human disease
inferredcites →https://doi.org/10.1038/ng.2504openalex-snapshot
Chromatin marks identify critical cell types for fine mapping complex trait variants
inferredcites →https://doi.org/10.1038/ng.406openalex-snapshot
The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling
inferredcites →https://doi.org/10.1038/nmeth.1906openalex-snapshot
ChromHMM: automating chromatin-state discovery and characterization
inferredcites →https://doi.org/10.1038/nmeth.1937openalex-snapshot
Unsupervised pattern discovery in human chromatin structure through genomic segmentation
inferredcites →https://doi.org/10.1038/nrg2905openalex-snapshot
Charting histone modifications and the functional organization of mammalian genomes
inferredcites →https://doi.org/10.1073/pnas.0909288106openalex-snapshot
The human insulin gene is part of a large open chromatin domain specific for human islets
inferredcites →https://doi.org/10.1073/pnas.1011775107openalex-snapshot
DNA search efficiency is modulated by charge composition and distribution in the intrinsically disordered tail
inferredcites →https://doi.org/10.1093/bioinformatics/bth456openalex-snapshot
GO::TermFinder—open source software for accessing Gene Ontology information and finding significantly enriched Gene Ontology terms associated with a list of genes
inferredcites →https://doi.org/10.1093/nar/gks1284openalex-snapshot
Integrative annotation of chromatin elements from ENCODE data
inferredcites →https://doi.org/10.1101/gr.100479.109openalex-snapshot
A CTCF-independent role for cohesin in tissue-specific transcription
inferredcites →https://doi.org/10.1101/gr.136184.111openalex-snapshot
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
inferredcites →https://doi.org/10.1126/science.1222794openalex-snapshot
Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
inferredcites →https://doi.org/10.1126/science.1228606openalex-snapshot
Mice Lacking a Myc Enhancer That Includes Human SNP rs6983267 Are Resistant to Intestinal Tumors
inferredcites →https://doi.org/10.1182/blood-2002-04-1104openalex-snapshot
Locus control regions
inferredcites →https://doi.org/10.1186/1471-2105-9-327openalex-snapshot
Gene Ontology term overlap as a measure of gene functional similarity
inferredcites →https://doi.org/10.1186/gm344openalex-snapshot
Pharmacogene regulatory elements: from discovery to applications
inferredcites →https://doi.org/10.1371/journal.pbio.1001046openalex-snapshot
A User's Guide to the Encyclopedia of DNA Elements (ENCODE)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Misregulation of Histone Methylation Regulators in Cancer
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DEEPFUSION: A Multimodal Deep Learning Approach for Super Enhancer Prediction
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Islet biology, the CDKN2A/B locus and type 2 diabetes risk
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Under-Evaluated or Unassessed Pathogenic Pathways in Autoimmune Hepatitis and Implications for Future Management
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STAT5-Driven Enhancers Tightly Control Temporal Expression of Mammary-Specific Genes
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Transcriptional Regulation of the Pancreatic Islet: Implications for Islet Function
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The β-Cell Genomic Landscape in T1D: Implications for Disease Pathogenesis
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The Role of STAT Signaling Pathways in the Pathogenesis of Systemic Lupus Erythematosus
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The structural and functional roles of CTCF in the regulation of cell type-specific and human disease-associated super-enhancers
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Genetics of Human Aging
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Genome-Wide DNA and Histone Modification Studies in Metabolic Disease
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The Epigenetics of Autoimmunity and Epigenetic Drug Discovery
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The epigenetics of pluripotent stem cells
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Genetic determinants of bone mass and osteoporotic fracture
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Transcriptional and Epigenomic Regulation of Lymphocytes
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ATAC-seq and psychiatric disorders
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Type 2 Diabetes Mellitus
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Pathobiology of Acute Lymphoblastic Leukemia
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“Enhancing” mechanosensing: Enhancers and enhancer-derived long non-coding RNAs in endothelial response to flow
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A Common Functional Regulatory Variant at a Type 2 Diabetes Locus Upregulates ARAP1 Expression in the Pancreatic Beta Cell
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Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits
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Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity
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Decreased STARD10 Expression Is Associated with Defective Insulin Secretion in Humans and Mice
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10 Years of GWAS Discovery: Biology, Function, and Translation
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A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression
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A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes
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Bromodomain and Extraterminal (BET) Proteins Regulate Hepatocyte Proliferation in Hepatocyte-Driven Liver Regeneration
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Atherosclerosis-associated differentially methylated regions can reflect the disease phenotype and are often at enhancers
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STAT signaling as a marker of SLE disease severity and implications for clinical therapy
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Super-enhancer lncs to cardiovascular development and disease
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Learning the Formation Mechanism of Domain-Level Chromatin States with Epigenomics Data
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A High-Resolution Map of Human Enhancer RNA Loci Characterizes Super-enhancer Activities in Cancer
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H3K4me3 Breadth Is Linked to Cell Identity and Transcriptional Consistency
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B Cell Super-Enhancers and Regulatory Clusters Recruit AID Tumorigenic Activity
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Convergent Transcription at Intragenic Super-Enhancers Targets AID-Initiated Genomic Instability
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Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay
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A Phase Separation Model for Transcriptional Control
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A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression
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Cohesin Loss Eliminates All Loop Domains
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Chromatin and gene-regulatory dynamics of the developing human cerebral cortex at single-cell resolution
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Genome-wide functional screen of 3′UTR variants uncovers causal variants for human disease and evolution
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Super-enhancers include classical enhancers and facilitators to fully activate gene expression
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Selective requirement of glycosphingolipid synthesis for natural killer and cytotoxic T cells
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Dynamic Recruitment of Functionally Distinct Swi/Snf Chromatin Remodeling Complexes Modulates Pdx1 Activity in Islet β Cells
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Inhibition of Super-Enhancer Activity in Autoinflammatory Site-Derived T Cells Reduces Disease-Associated Gene Expression
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T-bet Activates Th1 Genes through Mediator and the Super Elongation Complex
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The Super-Enhancer-Derived alncRNA-EC7/Bloodlinc Potentiates Red Blood Cell Development in trans
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Epigenomic Landscapes of hESC-Derived Neural Rosettes: Modeling Neural Tube Formation and Diseases
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Long-Range Enhancer Interactions Are Prevalent in Mouse Embryonic Stem Cells and Are Reorganized upon Pluripotent State Transition
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Transcriptional Dysregulation of MYC Reveals Common Enhancer-Docking Mechanism
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Multiomic Profiling Identifies cis-Regulatory Networks Underlying Human Pancreatic β Cell Identity and Function
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Activation of Oncogenic Super-Enhancers Is Coupled with DNA Repair by RAD51
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Hotspots of Aberrant Enhancer Activity in Fibrolamellar Carcinoma Reveal Candidate Oncogenic Pathways and Therapeutic Vulnerabilities
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Predicting mRNA Abundance Directly from Genomic Sequence Using Deep Convolutional Neural Networks
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Global Regulatory DNA Potentiation by SMARCA4 Propagates to Selective Gene Expression Programs via Domain-Level Remodeling
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Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretion
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Inhibiting an RBM39/MLL1 epigenomic regulatory complex with dominant-negative peptides disrupts cancer cell transcription and proliferation
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The dynamic landscape of enhancer-derived RNA during mouse early embryo development
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Selective control of HLA-DRB1 and HLA-DQA1 transcription through DR/DQ super enhancer microelements
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Systematic Analysis of the Determinants of Gene Expression Noise in Embryonic Stem Cells
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A Chromatin Basis for Cell Lineage and Disease Risk in the Human Pancreas
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Quantification, Dynamic Visualization, and Validation of Bias in ATAC-Seq Data with ataqv
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EpiMogrify Models H3K4me3 Data to Identify Signaling Molecules that Improve Cell Fate Control and Maintenance
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Systematic analysis identifies a connection between spatial and genomic variations of chromatin states
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Epstein-Barr Virus Oncoprotein Super-enhancers Control B Cell Growth
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Single-cell dissection of CD8+ T cell-driven immune dysregulation in type 1 diabetes mellitus: Mechanistic links to diabetic foot pathogenesis
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The epigenetics of PBC: The link between genetic susceptibility and environment
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FALCON systematically interrogates free fatty acid biology and identifies a novel mediator of lipotoxicity
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Functional interrogation of twenty type 2 diabetes-associated genes using isogenic human embryonic stem cell-derived β-like cells
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Multi-omic human pancreatic islet endoplasmic reticulum and cytokine stress response mapping provides type 2 diabetes genetic insights
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A CRISPR view of gene regulation
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Analysis of the landscape of human enhancer sequences in biological databases
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Dynamic Control of Enhancer Repertoires Drives Lineage and Stage-Specific Transcription during Hematopoiesis
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Single-cell chromatin accessibility identifies enhancer networks driving gene expression during spinal cord development in mouse
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Prediction of drug response and adverse drug reactions: From twin studies to Next Generation Sequencing
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SMC complexes link gene expression and genome architecture
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Transcriptional enhancers: functional insights and role in human disease
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Decoding the role of regulatory element polymorphisms in complex disease
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Somatic hypermutation mechanisms during lymphomagenesis and transformation
inferred← citeshttps://doi.org/10.1016/j.gendis.2020.12.012openalex-snapshot
BET bromodomain inhibitor JQ1 regulates spermatid development by changing chromatin conformation in mouse spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.gendis.2025.101652openalex-snapshot
Unveiling the regulatory potential of the non-coding genome: Insights from the human genome project to precision medicine
inferred← citeshttps://doi.org/10.1016/j.immuni.2019.03.028openalex-snapshot
The γc Family of Cytokines: Basic Biology to Therapeutic Ramifications
inferred← citeshttps://doi.org/10.1016/j.immuni.2025.10.020openalex-snapshot
FOXP3 expression depends on cell-type-specific cis-regulatory elements and transcription factor circuitry
inferred← citeshttps://doi.org/10.1016/j.it.2015.07.005openalex-snapshot
Super-enhancers: Asset management in immune cell genomes
inferred← citeshttps://doi.org/10.1016/j.it.2015.07.006openalex-snapshot
Exploiting genomics and natural genetic variation to decode macrophage enhancers
inferred← citeshttps://doi.org/10.1016/j.jaci.2017.12.1006openalex-snapshot
Epigenome analysis links gene regulatory elements in group 2 innate lymphocytes to asthma susceptibility
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101559openalex-snapshot
Unraveling three-dimensional chromatin structural dynamics during spermatogonial differentiation
inferred← citeshttps://doi.org/10.1016/j.jgg.2020.11.010openalex-snapshot
Fine genetic mapping of the chromosome 11q23.3 region in a Han Chinese population: insights into the apolipoprotein genes underlying the blood lipid-lipoprotein variances
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.12.045openalex-snapshot
From Genetic Association to Molecular Mechanisms for Islet-cell Dysfunction in Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/j.jmb.2020.07.023openalex-snapshot
Visualization and Sequencing of Accessible Chromatin Reveals Cell Cycle and Post-HDAC inhibitor Treatment Dynamics
inferred← citeshttps://doi.org/10.1016/j.mex.2020.101165openalex-snapshot
High-performance method for identification of super enhancers from ChIP-Seq data with configurable cloud virtual machines
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.05.016openalex-snapshot
The Mechanisms behind the Therapeutic Activity of BET Bromodomain Inhibition
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.08.024openalex-snapshot
NF-κB Directs Dynamic Super Enhancer Formation in Inflammation and Atherogenesis
inferred← citeshttps://doi.org/10.1016/j.molcel.2015.02.014openalex-snapshot
Convergence of Developmental and Oncogenic Signaling Pathways at Transcriptional Super-Enhancers
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.03.033openalex-snapshot
Bivalent Regions of Cytosine Methylation and H3K27 Acetylation Suggest an Active Role for DNA Methylation at Enhancers
inferred← citeshttps://doi.org/10.1016/j.molcel.2017.09.016openalex-snapshot
The Elongation Factor Spt6 Maintains ESC Pluripotency by Controlling Super-Enhancers and Counteracting Polycomb Proteins
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.04.025openalex-snapshot
Shaping Gene Expression by Landscaping Chromatin Architecture: Lessons from a Master
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.12.047openalex-snapshot
Temporal dissection of an enhancer cluster reveals distinct temporal and functional contributions of individual elements
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.12.032openalex-snapshot
Deciphering the multi-scale, quantitative cis-regulatory code
inferred← citeshttps://doi.org/10.1016/j.molmed.2016.10.004openalex-snapshot
Genomic Alterations of Non-Coding Regions Underlie Human Cancer: Lessons from T-ALL
inferred← citeshttps://doi.org/10.1016/j.molmet.2019.06.002openalex-snapshot
(Epi)genomic heterogeneity of pancreatic islet function and failure in type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.molmet.2019.12.006openalex-snapshot
Single-cell ATAC-Seq in human pancreatic islets and deep learning upscaling of rare cells reveals cell-specific type 2 diabetes regulatory signatures
inferred← citeshttps://doi.org/10.1016/j.mrrev.2024.108489openalex-snapshot
Super-enhancers: Implications in gastric cancer
inferred← citeshttps://doi.org/10.1016/j.nbd.2018.02.007openalex-snapshot
Parkinson's disease genetic risk in a midbrain neuronal cell line
inferred← citeshttps://doi.org/10.1016/j.neuron.2014.11.011openalex-snapshot
Genomic Perspectives of Transcriptional Regulation in Forebrain Development
inferred← citeshttps://doi.org/10.1016/j.neuron.2022.06.004openalex-snapshot
3D spatial genome organization in the nervous system: From development and plasticity to disease
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2015.07.004openalex-snapshot
Histone profiles in cancer
inferred← citeshttps://doi.org/10.1016/j.phrs.2023.106940openalex-snapshot
Super-enhancer-associated SNHG15 cooperating with FOSL1 contributes to bladder cancer progression through the WNT pathway
inferred← citeshttps://doi.org/10.1016/j.phrs.2026.108275openalex-snapshot
Targeting the transcriptional coactivator p300/CBP in cancer: Mechanistic insights and translational implications for osteosarcoma
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.07.008openalex-snapshot
Modeling three-dimensional genomic organization in evolution and pathogenesis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.05.007openalex-snapshot
CRISPR/Cas9 guided genome and epigenome engineering and its therapeutic applications in immune mediated diseases
inferred← citeshttps://doi.org/10.1016/j.stem.2014.05.004openalex-snapshot
Lost in Transition: Dynamic Enhancer Organization across Naive and Primed Stem Cell States
inferred← citeshttps://doi.org/10.1016/j.stem.2014.05.005openalex-snapshot
Epigenomic Comparison Reveals Activation of “Seed” Enhancers during Transition from Naive to Primed Pluripotency
inferred← citeshttps://doi.org/10.1016/j.stem.2019.11.011openalex-snapshot
Circadian Entrainment Triggers Maturation of Human In Vitro Islets
inferred← citeshttps://doi.org/10.1016/j.stemcr.2015.09.016openalex-snapshot
A Systematic Approach to Identify Candidate Transcription Factors that Control Cell Identity
inferred← citeshttps://doi.org/10.1016/j.stemcr.2019.04.004openalex-snapshot
Enhancer Chromatin and 3D Genome Architecture Changes from Naive to Primed Human Embryonic Stem Cell States
inferred← citeshttps://doi.org/10.1016/j.stemcr.2026.102930openalex-snapshot
ZFHX4 is necessary for dopaminergic neuron differentiation and controls cell cycle by regulating LIN28A
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.10.008openalex-snapshot
Distal enhancers: new insights into heart development and disease
inferred← citeshttps://doi.org/10.1016/j.tcb.2018.04.003openalex-snapshot
Enhancer Logic and Mechanics in Development and Disease
inferred← citeshttps://doi.org/10.1016/j.tcm.2015.01.014openalex-snapshot
The promise of enhancer-associated long noncoding RNAs in cardiac regeneration
inferred← citeshttps://doi.org/10.1016/j.tem.2014.05.001openalex-snapshot
The pancreatic β cell: recent insights from human genetics
inferred← citeshttps://doi.org/10.1016/j.tem.2016.11.005openalex-snapshot
Genome-Wide Insights into the Development and Function of Thermogenic Adipocytes
inferred← citeshttps://doi.org/10.1016/j.tibs.2022.01.002openalex-snapshot
The Mediator kinase module: an interface between cell signaling and transcription
inferred← citeshttps://doi.org/10.1016/j.tig.2014.02.006openalex-snapshot
Laying a solid foundation for Manhattan – ‘setting the functional basis for the post-GWAS era’
inferred← citeshttps://doi.org/10.1016/j.tig.2015.02.008openalex-snapshot
Epigenetic modifications and long noncoding RNAs influence pancreas development and function
inferred← citeshttps://doi.org/10.1016/j.tig.2015.11.004openalex-snapshot
Enhanced Identification of Transcriptional Enhancers Provides Mechanistic Insights into Diseases
inferred← citeshttps://doi.org/10.1016/j.tig.2016.02.003openalex-snapshot
Understanding Celiac Disease by Genomics
inferred← citeshttps://doi.org/10.1016/j.tig.2017.01.010openalex-snapshot
Genomics of Islet (Dys)function and Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/j.tig.2022.05.011openalex-snapshot
Interplay between regulatory elements and chromatin topology in cellular lineage determination
inferred← citeshttps://doi.org/10.1016/j.tig.2022.05.015openalex-snapshot
Transcriptional enhancers at 40: evolution of a viral DNA element to nuclear architectural structures
inferred← citeshttps://doi.org/10.1016/j.tma.2019.12.003openalex-snapshot
Remodeling of the H3 nucleosomal landscape during mouse aging
inferred← citeshttps://doi.org/10.1016/j.trecan.2016.09.002openalex-snapshot
Epigenomic Consequences of Coding and Noncoding Driver Mutations
inferred← citeshttps://doi.org/10.1016/j.trecan.2017.03.006openalex-snapshot
Super-Enhancer-Driven Transcriptional Dependencies in Cancer
inferred← citeshttps://doi.org/10.1016/j.xcrm.2022.100632openalex-snapshot
Intrinsic transcriptional heterogeneity in neuroblastoma guides mechanistic and therapeutic insights
inferred← citeshttps://doi.org/10.1016/j.xcrm.2024.101472openalex-snapshot
STAT3 couples activated tyrosine kinase signaling to the oncogenic core transcriptional regulatory circuitry of anaplastic large cell lymphoma
inferred← citeshttps://doi.org/10.1016/j.xgen.2024.100604openalex-snapshot
Implications of noncoding regulatory functions in the development of insulinomas
inferred← citeshttps://doi.org/10.1016/j.xgen.2025.100850openalex-snapshot
Incorporating multiple functional annotations to improve polygenic risk prediction accuracy
inferred← citeshttps://doi.org/10.1016/j.xgen.2025.101040openalex-snapshot
Predictive prioritization of enhancers associated with pancreatic disease risk
inferred← citeshttps://doi.org/10.1016/j.xhgg.2022.100158openalex-snapshot
CFDP1 is a neuroblastoma susceptibility gene that regulates transcription factors of the noradrenergic cell identity
inferred← citeshttps://doi.org/10.1016/j.xhgg.2026.100674openalex-snapshot
Massively parallel functional profiling prioritizes breast cancer risk variants and implicates CCDC88C in ER-positive breast cancer
inferred← citeshttps://doi.org/10.1016/j.ygeno.2014.04.006openalex-snapshot
Strategies to fine-map genetic associations with lipid levels by combining epigenomic annotations and liver-specific transcription profiles
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2019.04.012openalex-snapshot
Epigenetic therapies in heart failure
inferred← citeshttps://doi.org/10.1016/j.ymeth.2017.03.012openalex-snapshot
Mining the topography and dynamics of the 4D Nucleome to identify novel CNS drug pathways
inferred← citeshttps://doi.org/10.1017/s001667231600001xopenalex-snapshot
The future of iPS cells in advancing regenerative medicine
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c01100openalex-snapshot
Discovery of a Highly Potent PROTAC Degrader of p300/CBP Proteins for the Treatment of Enzalutamide-Resistant Prostate Cancer
inferred← citeshttps://doi.org/10.1021/acssynbio.4c00244openalex-snapshot
Enhancers: A Focus on Synthetic Biology and Correlated Gene Expression
inferred← citeshttps://doi.org/10.1038/leu.2014.70openalex-snapshot
Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myeloma
inferred← citeshttps://doi.org/10.1038/nature13835openalex-snapshot
Genetic and epigenetic fine mapping of causal autoimmune disease variants
inferred← citeshttps://doi.org/10.1038/nature14154openalex-snapshot
Super-enhancers delineate disease-associated regulatory nodes in T cells
inferred← citeshttps://doi.org/10.1038/nature15521openalex-snapshot
BCL11A enhancer dissection by Cas9-mediated in situ saturating mutagenesis
inferred← citeshttps://doi.org/10.1038/nature15540openalex-snapshot
Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism
inferred← citeshttps://doi.org/10.1038/nature18642openalex-snapshot
The genetic architecture of type 2 diabetes
inferred← citeshttps://doi.org/10.1038/nbt.3863openalex-snapshot
Characterization of noncoding regulatory DNA in the human genome
inferred← citeshttps://doi.org/10.1038/ncomms11764openalex-snapshot
The genetic regulatory signature of type 2 diabetes in human skeletal muscle
inferred← citeshttps://doi.org/10.1038/ncomms12092openalex-snapshot
Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci
inferred← citeshttps://doi.org/10.1038/ncomms12983openalex-snapshot
Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity
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