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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: Unclassified
ATCC
MeSH
RIKEN BRC
DRX202689
NextSeq 500 sequencing of SAMD00207114
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Unclassified
Cell type
Unclassified
NA
NA
Attributes by original data submitter
Sample
sample_name
Tet2KORx3_myc_input
strain
C57BL/6
genotype
Tet2-fl/fl;Cre-ERT2
infection
RUNX3
Sequenced DNA Library
library_name
Tet2KORx3_myc_input
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
NextSeq 500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
8785940
Reads aligned (%)
98.5
Duplicates removed (%)
58.0
Number of peaks
115 (qval < 1E-05)
mm9
Number of total reads
8785940
Reads aligned (%)
98.2
Duplicates removed (%)
58.3
Number of peaks
102 (qval < 1E-05)
Base call quality data from
DBCLS SRA