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Chromatin profiling following SWI/SNF inhibition in H295R or HEK 293T cells [ChIP-seq]

GSE260867 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 25 samples Submitted 2025/07/21 Platform GPL18573
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 25 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
Homo sapiens (human)
Samples
25 samples: 8 conditions, mostly in duplicateGroups 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
β-catenin functions as a molecular adapter for disordered cBAF interactionsMolecular cell · 2025
Summary (written by the submitters)
To assess the genome-wide effect of acute SWI/SNF inhibition on SF-1/β-catenin chromatin binding, we treated H295R or HEK 293T cells with 1 µM of SWI/SNF inhibitor BRM014 or DMSO vehicle control for 1 hour and performed ChIP-seq. Pronounced loss of chromatin occupancy was observed for SF-1 and β-catenin at enhancer sites bound by ARID1A-containing cBAF complexes.
Published in
β-catenin functions as a molecular adapter for disordered cBAF interactions
Chan YS, Gao Q, Robinson SA et al. · Molecular cell 2025 · PMID 40695292 · doi:10.1016/j.molcel.2025.06.026
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 GSE260867_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 PRJNA1083884 and SRA study SRP493418. Searching any of these in the dataset finder brings you back here.

Study design
8 conditions, mostly in duplicate
ChIP_SF1_H295R_DMSO ×2 ChIP_SF1_H295R_BRM014 ×2 ChIP_Bcat_H295R_DMSO ×2 ChIP_Bcat_H295R_BRM014 ×2 ChIP_p300_293T_DMSO ×2 ChIP_p300_293T_BRM014 ×2 ChIP_p300_H295R_DMSO ×2 ChIP_p300_H295R_BRM014 ×2 +9 more

Supports a between-group comparison across 16 samples.

How we read this: 8 replicated groups read from 25 sample titles; they account for 16 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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