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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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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: Rad21
wikigenes
PDBj
CellType: CH12F3
ATCC
MeSH
RIKEN BRC
SRX6708980
GSM4030108: CH12F3NCdel aCD40 IL4 TGFb Rad21 4; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
Rad21
Cell type
Cell type Class
Blood
Cell type
CH12F3
NA
NA
Attributes by original data submitter
Sample
source_name
CH12F3 murine lymphoma cells
cell type
AID-deficient Splenic mature B cells
passages
8--17
strain
C57BL/6
chip antibody
Rad21 (Abcam, ab992)
treatment
with aCD40/IL4/TGFb stimulation
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared according to Illumina's instructions accompanying the TruSeq ChIP Library Preparation Kit (IP-202-1012).
Sequencing Platform
instrument_model
NextSeq 550
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
45620719
Reads aligned (%)
98.2
Duplicates removed (%)
33.1
Number of peaks
23212 (qval < 1E-05)
mm9
Number of total reads
45620719
Reads aligned (%)
98.1
Duplicates removed (%)
33.4
Number of peaks
23241 (qval < 1E-05)
Base call quality data from
DBCLS SRA