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Install and launch IGV before selecting data to visualize
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For hg38
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For hg19
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
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: T-ALL
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX107292
GSM837991: Input WCE ChIP-seq Prima5 T-ALL 1
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Blood
Cell type
T-ALL
NA
NA
Attributes by original data submitter
Sample
source_name
T-ALL primagraft
chip antibody
None
antibody catalog number
None WCE
sample type
T-ALL primagraft 05-386
Sequenced DNA Library
library_name
GSM837991: Input WCE ChIP-seq Prima5 T-ALL 1
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
hg38
Number of total reads
13995500
Reads aligned (%)
78.1
Duplicates removed (%)
70.2
Number of peaks
151 (qval < 1E-05)
hg19
Number of total reads
13995500
Reads aligned (%)
77.5
Duplicates removed (%)
71.5
Number of peaks
188 (qval < 1E-05)
Base call quality data from
DBCLS SRA