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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: Pfeiffer
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX188592
GSM1006150: Input Pfeiffer; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Blood
Cell type
Pfeiffer
Primary Tissue
Blood
Tissue Diagnosis
Hodgkin's Lymphoma
Attributes by original data submitter
Sample
source_name
Pfeiffer
cell line
Pfeiffer
genotype/variation
EZH2 mutant
average gic50
28 nM
chip antibody
Input control
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer II
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
41201766
Reads aligned (%)
99.3
Duplicates removed (%)
17.8
Number of peaks
1187 (qval < 1E-05)
hg19
Number of total reads
41201766
Reads aligned (%)
98.5
Duplicates removed (%)
18.9
Number of peaks
1250 (qval < 1E-05)
Base call quality data from
DBCLS SRA