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Endogenous fine-mapping of functional regulatory elements in complex genetic loci in HAP1

GSE286226 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 59 samples Submitted 2025/01/10 Platform GPL24676
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 59 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
59 samples: 40 distinct titles, 10 of them repeatedGroups 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
Endogenous fine-mapping and prioritization of functional regulatory elements in complex genetic lociCell genomics · 2025
SuperSeries — this record groups several sub-series.
Summary (written by the submitters)
This SuperSeries is composed of the SubSeries listed below.
Published in
Endogenous fine-mapping and prioritization of functional regulatory elements in complex genetic loci
Zhao K, Zhou Y, Wang X et al. · Cell genomics 2025 · PMID 40882622 · doi:10.1016/j.xgen.2025.100982
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 GSE286226_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 PRJNA1208702 and SRA study SRP554139. Searching any of these in the dataset finder brings you back here.

Study design
40 distinct titles, 10 of them repeated
HAP1,Micro-C ×6 CRISPRi, transcriptomes scRNA-seq, ×3 CRISPRko, transcriptomes scRNA-seq, ×3 CRISPRa, transcriptomes scRNA-seq, ×3 CRISPRa, sgRNA enrichment scRNA-seq, ×3 CRISPRko, sgRNA enrichment scRNA-seq, ×3 CRISPRi, sgRNA enrichment scRNA-seq, ×2 HAP1,wild-type, H3K4me ×2 +2 more

How we read this: Read from 59 sample titles: 40 distinct titles with little repetition. 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

+ 19 more — browse all 59 samples with per-sample file links →

Datasets on a similar topic

Search all human RNA-seq datasets in GEO →

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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.