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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: Input control
wikigenes
PDBj
CellType: Granulocytic-monocytic progenitors
ATCC
MeSH
RIKEN BRC
DRX002667
TET2KO input
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Blood
Cell type
Granulocytic-monocytic progenitors
NA
NA
Attributes by original data submitter
Sample
sample_name
DRS002762
sample comment
GMPs from TET2 KO input
Sequenced DNA Library
library_name
TET2KO input
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
79770870
Reads aligned (%)
88.7
Duplicates removed (%)
13.9
Number of peaks
777 (qval < 1E-05)
mm9
Number of total reads
79770870
Reads aligned (%)
88.5
Duplicates removed (%)
13.8
Number of peaks
896 (qval < 1E-05)
Base call quality data from
DBCLS SRA