Hypoxic regulation of chromatin and gene transcription
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 98 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
- 98 samples: 98 samples, each with a distinct title — no replicated groupsGroups 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
- Hypoxic regulation of chromatin and gene transcriptionCommunications biology · 2026
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.
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.
Supplementary files
The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE296192_RAW.tar (it can run to tens of gigabytes).
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 PRJNA1258176 and SRA study SRP582782. Searching any of these in the dataset finder brings you back here.
Any grouping that defines a comparison lives in the sample characteristics, which GEO records separately from the titles.
How we read this: Read from 98 sample titles: 98 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.
- GSM8966647 PC3_1_Nx_rep1_K4me3
- GSM8966648 PC3_2_Hx_rep1_K4me3
- GSM8966649 PC3_3_Nx_rep2_K4me3
- GSM8966650 PC3_4_Hx_rep2_K4me3
- GSM8966651 PC3_5_Nx_rep1_K9me3
- GSM8966652 PC3_6_Hx_rep1_K9me3
- GSM8966653 PC3_7_Nx_rep2_K9me3
- GSM8966654 PC3_8_Hx_rep2_K9me3
- GSM8966655 PC3_9_Nx_rep1_K27me3
- GSM8966656 PC3_10_Hx_rep1_K27me3
- GSM8966657 PC3_11_Nx_rep2_K27me3
- GSM8966658 PC3_12_Hx_rep2_K27me3
- GSM8966659 PC3_13_Nx_rep1_K36me3
- GSM8966660 PC3_14_Hx_rep1_K36me3
- GSM8966661 PC3_15_Nx_rep2_K36me3
- GSM8966662 PC3_16_Hx_rep2_K36me3
- GSM8966663 PC3_17_Nx_rep1_H3
- GSM8966664 PC3_18_Hx_rep1_H3
- GSM8966665 PC3_19_Nx_rep2_H3
- GSM8966666 PC3_20_Hx_rep2_H3
- GSM8966667 PC3_21_Nx_rep1_input
- GSM8966668 PC3_22_Hx_rep1_input
- GSM8966669 PC3_23_Nx_rep2_input
- GSM8966670 PC3_24_Hx_rep2_input
- GSM8966671 PC3_1_Parental_Nx_K4me3
- GSM8966672 PC3_2_Parental_Hx_K4me3
- GSM8966673 PC3_3_HIF1bKOclone13_Nx_K4me3
- GSM8966674 PC3_4_HIF1bKOclone13_Hx_K4me3
- GSM8966675 PC3_5_HIF1bKOclone19_Nx_K4me3
- GSM8966676 PC3_6_HIF1bKOclone19_Hx_K4me3
- GSM8966678 PC3_7_Parental_Nx_K9me3
- GSM8966682 PC3_8_Parental_Hx_K9me3
- GSM8966685 PC3_9_HIF1bKOclone13_Nx_K9me3
- GSM8966689 PC3_10_HIF1bKOclone13_Hx_K9me3
- GSM8966694 PC3_11_HIF1bKOclone19_Nx_K9me3
- GSM8966696 PC3_12_HIF1bKOclone19_Hx_K9me3
- GSM8966698 PC3_13_Parental_Nx_K27me3
- GSM8966699 PC3_14_Parental_Hx_K27me3
- GSM8966700 PC3_15_HIF1bKOclone13_Nx_K27me3
- GSM8966701 PC3_16_HIF1bKOclone13_Hx_K27me3
+ 58 more — browse all 98 samples with per-sample file links →
- GSE296190 Hypoxic regulation of chromatin and gene transcription [ChIP-seq] 84 samples shares transcription, chromatin, hypoxic
- GSE303478 Systematic investigation reveals extensive Epstein-Barr virus transcriptional regulation of the human genome 217 samples shares transcription
- GSE328578 CBFA2T3-GLIS2 fusion-mediated mSWI/SNF chromatin remodeler disruption generates cancer-specific dependencies in AMKL 156 samples shares chromatin
- GSE306993 Transcriptional and epigenetic targets of MEF2C in human microglia contribute to cellular functions related to autism risk and age-related disease. 76 samples shares transcription
- GSE272562 Dynamic activation of rAAV transgene expression by a small molecule that recruits endogenous transcriptional machinery 46 samples shares transcription
- GSE303855 Mechanistic and Epigenetic Partitioning of Lamina-Associated Chromatin Revealed by a Genome-Wide Imaging Screen 45 samples shares chromatin
- GSE275631 Characterization of E2F8-mediated transcriptional regulation in lethal prostate cancer 39 samples shares transcription
- GSE244585 Single nuclei chromatin accessibility and transcriptomic map of breast tissues of women of diverse genetic ancestry [10X single-cell multiome] 32 samples shares chromatin
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.