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Install and launch IGV before selecting data to visualize
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For mm10
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For mm9
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Link Out
Sequence Read Archive
DBCLS SRA
NCBI SRA
ENA
Antigen: H3K27me3
wikigenes
PDBj
CellType: CD4 CD8 double positive cells
ATCC
MeSH
RIKEN BRC
SRX018112
GSM523694: DP-Gata3-KO-H3K27me3 [Methyl-Seq]
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Histone
Antigen
H3K27me3
Cell type
Cell type Class
Blood
Cell type
CD4 CD8 double positive cells
NA
NA
Attributes by original data submitter
Sample
source_name
Double positive cells
strain
C57BL/6
genotype/variation
Gata3 knockout
cell type
Double-positive cells
antibody
anti-H3K27me3
Sequenced DNA Library
library_name
DP-Gata3-KO-H3K27me3 [Methyl-Seq]
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer II
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
12863697
Reads aligned (%)
91.7
Duplicates removed (%)
19.6
Number of peaks
2205 (qval < 1E-05)
mm9
Number of total reads
12863697
Reads aligned (%)
91.5
Duplicates removed (%)
19.7
Number of peaks
2204 (qval < 1E-05)
Base call quality data from
DBCLS SRA