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Chromatin atlas maps regulatory elements linked to Crohn's disease

Figure 1: Yu Zhao et al. Single-cell analysis of chromatin accessibility in the human intestine identifies regulatory programs and clarifies genetic associations in Crohn’s disease. Nature Genetics (2026).Image licenceFull-size image

Researchers built an atlas of 557,310 candidate cis-regulatory elements from mucosal samples from 23 Crohn's disease patients and 16 healthy controls, covering the human terminal ileum and ascending colon. The paper, published in Nature Genetics, used single-cell ATAC-seq to track regulatory programs during intestinal inflammation. Heritability for Crohn's disease concentrated mostly in immune cells, particularly T cells and neutrophils. Fine mapping pinpointed 30 noncoding disease variants sitting directly within those regulatory elements.

The atlas gives researchers a reference for studying how noncoding risk variants affect gene regulation in cells from Crohn's patients.

Written by the Genomes desk from the primary source cited and linked above and checked against it. Research use only; not medical advice. Corrections: [email protected].

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