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SCREATE

Single-Cell Regulatory Elements And Traits Encyclopedia

SCREATE

Explore the regulatory landscape of human cells in the context of cell identity and traits.

Connect cell identity, genes and regulatory elements with thousands of human traits. One atlas, linking single cells to traits through the genome. Move seamlessly between UMAPs, lists, heatmaps and genome browsers, and ask AI agents to help interpret the cellular and molecular basis of human disease susceptibility.

34 cell types 152 subtypes 30 tissue contexts

The atlas at a glance

From cells to regulatory context
Human cells
1,237,504
Across 30 tissue contexts
tCREs
526,448
Regulatory elements
Cell states
688
Within 34 major cell types
Individual traits
12,313
Combined into 5,288 meta traits

Explore SCREATE

Start with a question.

Follow a cell, a gene or a trait.
Move between connected views of the atlas.

From patterns to interpretation

Interpret the contexts with AI

Open an example, then click the highlighted star.
SCREATE’s association contexts between traits, cells, and genes will be sent to AI for interpretation.

The illustrations are schematic. Each example opens SCREATE first; only clicking its star sends the prepared prompt to Google AI Mode. AI interpretations should be checked against the evidence and cited sources.

Try an example

Connect cells, traits and genes.

Two complementary browsers for each example.
Explore more for new associations and perspectives.

Each card combines two of Cell Browser, Trait Browser and Genome Browser. Trait Browser examples open a trait–cell or trait–gene pair, or all traits associated with a cell or gene. Where available, use Cell scope to compare relevant cellular contexts. These are exploratory associations, not proof of causality. Protein-level/ratio traits are excluded. Both links open in new tabs.

Open resources

Take the atlas further.

Explore the underlying data,
methods and analysis code.

Read the cell-type annotations. Browse marker genes, biological rationales and functional descriptions for every type, subtype and state, without loading the interactive browsers.

Cell annotations