Super Enhancer Identification for Functional Genomics and Disease Mechanism Research
Reveal the genome's most powerful regulatory regions with our Super Enhancer Identification Service. At CD Genomics, we generate high-resolution maps of super enhancers—extended enhancer clusters enriched for transcription factors, Mediator, BRD4, and H3K27ac—that play decisive roles in cell fate determination, lineage specification, and disease-associated gene activation.
From dissecting transcriptional control in stem cell systems, to mapping oncogenic drivers in cancer models, to uncovering non-coding variant hotspots in complex traits, our integrated sequencing and bioinformatics platform delivers publication-ready datasets and biological insights you can directly apply to your research.
Partner with us to design an assay strategy that matches your sample constraints and scientific goals.
From Cell Identity to Disease: Why Super Enhancers Matter
Super enhancers (SEs) are not ordinary regulatory elements—they are large, high-density clusters of enhancers spanning tens of kilobases, each densely bound by master transcription factors, Mediator complexes, BRD4, and enriched with activating histone marks such as H3K27ac. Their unique architecture enables them to orchestrate exceptionally high levels of transcription for genes that define cell identity or drive disease processes.
A Central Node in the Regulatory Genome
Cell fate control – SEs regulate genes essential for lineage commitment, differentiation, and tissue identity.
Disease driver loci – Many cancer-associated genes and disease-linked variants cluster within SE regions, making them hotspots for functional genomics studies.
Transcriptional addiction – Cells often rely disproportionately on SE-driven gene programs, making SEs valuable for discovering vulnerability points in disease models.
A Gateway to Mechanistic Insights
By mapping SE landscapes under different biological conditions—such as development, environmental stress, or targeted perturbations—researchers can uncover:
Shifts in the regulatory network that accompany cellular reprogramming
Activation or silencing of SEs in tumor progression and metastasis
How non-coding genetic variants influence enhancer activity and gene expression patterns
At CD Genomics, we combine high-resolution sequencing with expert bioinformatics to produce SE maps that go beyond static annotation. We help you connect SE locations to functional targets, transcriptional circuits, and pathway context, enabling data-driven hypotheses for your next experimental step.
Technologies
Two Ways In, One Clear Map: ChIP-seq vs. CUT&Tag
Super enhancer mapping can be achieved through multiple experimental strategies, but choosing the right approach for your samples and research goals is essential for generating reliable, high-impact data. At CD Genomics, we offer two complementary methods—ChIP-seq and CUT&Tag—each optimized for different experimental contexts.
ChIP-seq: The Gold Standard for Comprehensive Mapping
Best for:high-input samples (e.g., ≥ 107 cells), crosslinked tissue, or projects needing established antibody validation.
How it works: Chromatin immunoprecipitation enriches DNA bound by your target (H3K27ac, BRD4, Mediator, or TFs), followed by deep sequencing and ROSE based enhancer stitching.
Strengths:
Extensive literature validation and reproducibility across species
High compatibility with additional histone marks or transcription factor profiling
Well-established bioinformatics pipeline for super enhancer ranking
Considerations:
Requires more material and processing time
Slightly higher background due to crosslinking and sonication
CUT&Tag: Precision Mapping for Low-Input or Fragile Samples
Best for: limited cell numbers (~2 × 105 cells), rare cell types, or fresh/frozen tissues requiring gentle handling.
How it works: Antibodies guide a Tn5 transposase directly to the target chromatin in situ, simultaneously cleaving and adding sequencing adapters at binding sites.
Strengths:
High signal-to-noise ratio with minimal background
One-tube workflow reduces handling errors and sample loss
Suitable for histone modifications, many transcription factors, and even clinical-grade primary samples in a research context
Considerations:
Requires high-specificity antibodies for optimal results
Slightly less historical benchmarking compared to ChIP-seq for certain rare marks
Not Sure Which to Choose?
Features
ChIP-seq
CUT&Tag
Sample Requirements
High (≥107 cells)
Low (2×105 or fewer)
Background Signal
Moderate to High
Extremely Low
Procedure Steps
Multiple steps, including crosslinking, shearing, IP, etc.
Simplified, one-tube process
Historical Maturity
High, widely validated
Emerging but growing rapidly
Applicable Scenarios
Compatible with multiple targets and sample types
Precise and sensitive, suitable for fragile/rare samples
Our team can assess your sample availability, target type, and downstream analysis needs to recommend the optimal strategy—or even run both methods in parallel for cross validation.
With either approach, you receive high-resolution, genome-wide SE maps, annotated gene targets, and downstream network analysis, enabling you to confidently move from raw data to actionable biological insight.
Service Workflow
What Happens in Our Labs: End-to-End Pipeline
From your first inquiry to final data, every step is built to give you clear, reproducible, and publication-ready results.
We start with your goals. You tell us your target histone marks or transcription factors, we match them with proven antibodies and the right method—ChIP-seq or CUT&Tag—based on your sample type and quantity.
Your samples are checked before we proceed. We make sure integrity and quality meet the standards needed for reliable sequencing.
We run optimized chromatin profiling. Whether through ChIP-seq or CUT&Tag, our protocols are tuned to capture high-confidence enhancer signals with minimal background noise.
We process and analyze your data in-house. From read alignment to enhancer stitching and super enhancer ranking, all analysis follows a transparent, well-validated pipeline.
You get more than just files. We deliver a full report with ranked SEs, predicted target genes, pathway analysis, and ready-to-use visualizations—so you can move straight to interpretation and publication.
Bioinformatics
We Deliver Biological Insights, Not Just Data
Our super enhancer identification service is designed to give you clear answers, not just raw sequencing files. Every project includes a complete, publication-ready analysis package, so you can go from data delivery to interpretation without additional processing.
From ChIP-seq and CUT&Tag data, you receive:
Enhancer classification & comparison – Distinguish typical enhancers and super enhancers with length and count statistics, plus genomic location and feature comparisons.
Visualized super enhancer landscapes – Plots showing SE numbers, distribution across the genome, and ChIP-seq/CUT&Tag signal intensity profiles.
Regulatory partner prediction – Motif enrichment analysis to identify transcription factors likely driving SE activity.
Core regulatory circuitry (CRC) analysis – Identify master TF networks anchored by SEs in your system.
Target gene mapping & functional relevance – Annotation of potential SE-regulated genes, linking them to biological processes and disease pathways.
GO & KEGG enrichment – Functional and pathway context for SE-linked genes, revealing their roles in cell identity, signaling, or pathology.
Genome browser–ready tracks & QC plots – IGV peak views, library quality metrics, read coverage plots, and transcription start site heatmaps for transparency and reproducibility.
Our analysis is not one-size-fits-all—we tailor outputs to your experimental design and research goals, ensuring you get insights that directly support your hypotheses and publications.
Applications
Where Super Enhancer Mapping Can Transform Your Research
Super enhancer profiling is more than an epigenomic map—it's a gateway to uncovering the regulatory architecture that shapes gene expression and cellular identity. Our service empowers diverse research areas, giving you actionable data for targeted experiments and hypothesis generation.
Decoding cell fate decisions
Track SE activation and silencing during stem cell differentiation or lineage commitment.
Uncovering oncogenic drivers
Identify SE-linked oncogenes and core transcription factor circuits that sustain tumor growth.
Connecting non-coding variants to function
Overlay GWAS or variant datasets to pinpoint regulatory mutations in SE regions.
Comparative epigenomics
Detect shifts in SE landscapes across developmental stages, environmental stresses, or genetic perturbations.
Building regulatory network models
Integrate SE maps with transcriptomics to define master regulatory nodes and pathways.
By targeting the most influential regulatory elements in the genome, SE mapping can help you move from descriptive to mechanistic insights—turning sequencing data into discoveries that shape the next phase of your research.
Sample Requirements
Sample Requirements
Parameter
ChIP-seq
CUT&Tag
Sample type
Cells or tissue
Fresh/frozen cells or tissue
Cell number
≥ 1 × 107 cells
≥ 2 × 105 cells
Antibody
ChIP-grade for target histone mark/TF
CUT&Tag-validated for target histone mark/TF
Fixation
Formaldehyde crosslinking required
No crosslinking; nuclei integrity required
Storage
Flash-frozen in liquid nitrogen or dry ice
Same as ChIP-seq; avoid repeated freeze-thaw
Shipping
On dry ice, overnight courier
On dry ice, overnight courier
If you are unsure whether your material meets these requirements, our technical team can provide guidance before you ship.
Advantages
Why CD Genomics Is Your Best Partner
Choosing a super enhancer identification service is about more than just running a protocol—it's about trusting the quality of every decision made from sample to result.
Method flexibility without bias
We recommend ChIP-seq or CUT&Tag based purely on your sample characteristics and research goals, not on internal convenience.
Proven antibody sourcing
Access to rigorously tested, project-specific antibodies from trusted suppliers ensures higher signal specificity and reproducibility.
Integrated wet-lab and bioinformatics teams
Direct communication between experimental and computational scientists keeps every dataset coherent from bench to analysis.
Transparent quality checkpoints
We share QC plots, peak quality metrics, and coverage profiles so you can independently evaluate data robustness.
Customizable deliverables
Beyond standard SE maps, we can include comparative analyses, condition-specific SE shifts, or integration with your own datasets.
Confidential, publication-ready outputs
Data and results are delivered in open formats with no proprietary lock-in, ready for immediate inclusion in figures, manuscripts, or grant reports.
Our role is not just to generate data, but to serve as an extension of your research team—anticipating analytical needs, identifying potential pitfalls early, and ensuring your project reaches a stage where the results can drive meaningful scientific conclusions.
