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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)
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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: Max
wikigenes
PDBj
CellType: Lung tumors
ATCC
MeSH
RIKEN BRC
SRX7849443
GSM4379842: MAX IP in sgCtrl preSC Rep1; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
Max
Cell type
Cell type Class
Lung
Cell type
Lung tumors
NA
NA
Attributes by original data submitter
Sample
source_name
preSC
genotype
Chga-GFP;Rblox/lox;p53lox/lox;p130lox
transduction
sgRNA control
antibody
MAX Proteintech 10426-1-AP; RRID: AB_2141660
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Cells were crosslinked in formaldehyde and ChIP was performed Libraries were constructed using the NEB Ultra II kit for Illumina
Sequencing Platform
instrument_model
Illumina HiSeq 2500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
36164999
Reads aligned (%)
97.0
Duplicates removed (%)
9.1
Number of peaks
246 (qval < 1E-05)
mm9
Number of total reads
36164999
Reads aligned (%)
96.8
Duplicates removed (%)
10.0
Number of peaks
251 (qval < 1E-05)
Base call quality data from
DBCLS SRA