Epigenetic changes by EZH2 inhibition increase translocations in B cells with high AID activity or DNA repair deficiency
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 130 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
- 130 samples: 21 conditions, mostly with about 5 replicates eachGroups 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
- Epigenetic changes by EZH2 inhibition increase translocations in B cells with high AID activity or DNA repair deficiencyBlood · 2025
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 GSE266298_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 PRJNA1106523 and SRA study SRP504863. Searching any of these in the dataset finder brings you back here.
Supports a between-group comparison across 122 samples.
How we read this: 21 replicated groups read from 130 sample titles; they account for 122 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.
- GSM8242253 CH12F3_Ligase4-KO_DMSO_1 CH12F3_Ligase4-KO_DMSO
- GSM8242254 CH12F3_Ligase4-KO_DMSO_2 CH12F3_Ligase4-KO_DMSO
- GSM8242255 CH12F3_Ligase4-KO_DMSO_3 CH12F3_Ligase4-KO_DMSO
- GSM8242256 CH12F3_Ligase4-KO_Tazemetostat_1 CH12F3_Ligase4-KO_Tazem…
- GSM8242257 CH12F3_Ligase4-KO_Tazemetostat_2 CH12F3_Ligase4-KO_Tazem…
- GSM8242258 CH12F3_Ligase4-KO_Tazemetostat_3 CH12F3_Ligase4-KO_Tazem…
- GSM8242259 CH12F3_Ligase4-KO_Valemetostat_1 CH12F3_Ligase4-KO_Valem…
- GSM8242260 CH12F3_Ligase4-KO_Valemetostat_2 CH12F3_Ligase4-KO_Valem…
- GSM8242261 CH12F3_Ligase4-KO_Valemetostat_3 CH12F3_Ligase4-KO_Valem…
- GSM8242274 CH12F3_AID-KO_DMSO_1 CH12F3_AID-KO_DMSO
- GSM8242275 CH12F3_AID-KO_DMSO_2 CH12F3_AID-KO_DMSO
- GSM8242276 CH12F3_AID-KO_DMSO_3 CH12F3_AID-KO_DMSO
- GSM8242277 CH12F3_AID-KO_Tazemetostat_1 CH12F3_AID-KO_Tazemetos…
- GSM8242278 CH12F3_AID-KO_Tazemetostat_2 CH12F3_AID-KO_Tazemetos…
- GSM8242279 CH12F3_AID-KO_Tazemetostat_3 CH12F3_AID-KO_Tazemetos…
- GSM8242280 CH12F3_AID-KO_Valemetostat_1 CH12F3_AID-KO_Valemetos…
- GSM8242281 CH12F3_AID-KO_Valemetostat_2 CH12F3_AID-KO_Valemetos…
- GSM8242282 CH12F3_AID-KO_Valemetostat_3 CH12F3_AID-KO_Valemetos…
- GSM8242879 CH12F3_AID-KO_DMSO-1 CH12F3_AID-KO_DMSO
- GSM8242880 CH12F3_AID-KO_DMSO-2 CH12F3_AID-KO_DMSO
- GSM8242881 CH12F3_AID-KO_DMSO-3 CH12F3_AID-KO_DMSO
- GSM8242882 CH12F3_AID-KO_DMSO-4 CH12F3_AID-KO_DMSO
- GSM8242883 CH12F3_AID-KO_DMSO-5 CH12F3_AID-KO_DMSO
- GSM8242884 CH12F3_AID-KO_Tazemetostat-1 CH12F3_AID-KO_Tazemetos…
- GSM8242885 CH12F3_AID-KO_Tazemetostat-2 CH12F3_AID-KO_Tazemetos…
- GSM8242886 CH12F3_AID-KO_Tazemetostat-3 CH12F3_AID-KO_Tazemetos…
- GSM8242887 CH12F3_AID-KO_Tazemetostat-4 CH12F3_AID-KO_Tazemetos…
- GSM8242888 CH12F3_AID-KO_Valemetostat-1 CH12F3_AID-KO_Valemetos…
- GSM8242889 CH12F3_AID-KO_Valemetostat-2 CH12F3_AID-KO_Valemetos…
- GSM8242890 CH12F3_AID-KO_Valemetostat-3 CH12F3_AID-KO_Valemetos…
- GSM8242891 CH12F3_AID-WT_DMSO_1 CH12F3_AID-WT_DMSO
- GSM8242892 CH12F3_AID-WT_DMSO_2 CH12F3_AID-WT_DMSO
- GSM8242893 CH12F3_AID-WT_DMSO_3 CH12F3_AID-WT_DMSO
- GSM8242894 CH12F3_AID-WT_DMSO_4 CH12F3_AID-WT_DMSO
- GSM8242895 CH12F3_AID-WT_DMSO_5 CH12F3_AID-WT_DMSO
- GSM8242896 CH12F3_AID-WT_Idelalisib_DMSO-1 CH12F3_AID-WT_Idelalisi…
- GSM8242897 CH12F3_AID-WT_Idelalisib_DMSO-2 CH12F3_AID-WT_Idelalisi…
- GSM8242898 CH12F3_AID-WT_Idelalisib_DMSO-3 CH12F3_AID-WT_Idelalisi…
- GSM8242899 CH12F3_AID-WT_Idelalisib_DMSO-4 CH12F3_AID-WT_Idelalisi…
- GSM8242900 CH12F3_AID-WT_Idelalisib_DMSO-5 CH12F3_AID-WT_Idelalisi…
+ 90 more — browse all 130 samples with per-sample file links →
- GSE218717 EZH2 gain-of-function mutations distort H3K27me3 landscapes and transform transcriptional responses to PRC2 inhibition. 244 samples shares ezh2, inhibition
- GSE218716 EZH2 gain-of-function mutations distort H3K27me3 landscapes and transform transcriptional responses to PRC2 inhibition [ChIP-Seq/Cut&Run-Seq] 156 samples shares ezh2, inhibition
- GSE261746 EZH2 INHIBITION ENHANCES T CELL IMMUNOTHERAPIES BY INDUCING LYMPHOMA IMMUNOGENICITY AND IMPROVING T CELL FUNCTION 54 samples shares ezh2, inhibition
- GSE255548 EZH2 INHIBITION ENHANCES T CELL IMMUNOTHERAPIES BY INDUCING LYMPHOMA IMMUNOGENICITY AND IMPROVING T CELL FUNCTION (RNA-Seq) 35 samples shares ezh2, inhibition
- GSE278481 EZH2 INHIBITION ENHANCES T CELL IMMUNOTHERAPIES BY INDUCING LYMPHOMA IMMUNOGENICITY AND IMPROVING T CELL FUNCTION (CUT&RUN) 16 samples shares ezh2, inhibition
- GSE71225 EZH2 inhibition as a targeted therapy for H3K27M mutant pediatric gliomas [ChIP-seq] 13 samples shares ezh2, inhibition
- GSE185152 The RANBP2/Importin-7-FOXO1 axis provides superior cold protection to aid islet transplantation 89 samples shares aid
- GSE287355 An EZH2—SREBP2 axis promotes cholesterol biosynthesis and represents a noncanonical vulnerability in tumorigenesis 79 samples shares ezh2
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.