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A hierarchical Rorc(γt) cis-regulatory cascade orchestrates differentiation of RORγt⁺ innate immune cells [ATAC-seq]

GSE278157 Mus musculus (mouse) ChIP-seq / ATAC-seq (genome binding and open chromatin) 40 samples Submitted 2026/03/24 Platform GPL17021
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · mouse · 40 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Mus musculus (mouse)
Samples
40 samples: 11 conditions, mostly in triplicateGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
A hierarchical Rorc(γt) cis-regulatory cascade orchestrates differentiation of RORγt⁺ innate immune cellsImmunity · 2026
Summary (written by the submitters)
Although ILC3s are known to differentiate in RORγt-dependent manner, besides ILC3s, RORγt-dependent developmental program is shared among several lymphocytes.However, little is known about the regulatory mechanism of RORγt expression specific to ILC3s. Our data newly idetified cell lineage-specific and two-step regulation of RORγt expression in ILC3 including LTi cells.
Published in
A hierarchical Rorc(γt) cis-regulatory cascade orchestrates differentiation of RORγt⁺ innate immune cells
Fukui T, Watanabe M, Kobayashi R et al. · Immunity 2026 · PMID 41881028 · doi:10.1016/j.immuni.2026.02.002
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE278157_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA1165774 and SRA study SRP536177. Searching any of these in the dataset finder brings you back here.

Study design
11 conditions, mostly in triplicate
fetal liver, E14.5, ATAC-seq, RORgtKO_RORgt_n… ×6 fetal liver, E14.5, ATAC-seq, RORgtKO_RORgt_m… ×6 fetal liver, E14.5, ATAC-seq, CD127pos_Runx3n… ×3 fetal liver, E14.5, ATAC-seq, CD127pos_Runx3p… ×3 fetal liver, E14.5, ATAC-seq, RORgt_high_CD12… ×3 fetal liver, E14.5, ATAC-seq, RORgt_high_CD12… ×3 fetal liver, E14.5, ATAC-seq, RORgt_high_CD12… ×3 fetal liver, E14.5, ATAC-seq, RORgt_neg ×2 +8 more

Supports a between-group comparison across 35 samples.

How we read this: 11 replicated groups read from 40 sample titles; they account for 35 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
Datasets on a similar topic

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.