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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)
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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: Tumor
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX4679529
GSM3389352: ATRX in-frame fusion neuroblastoma. Patient SJNBL047443 Input XL; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Others
Cell type
Tumor
NA
NA
Attributes by original data submitter
Sample
source_name
Tumor Tissue
tissue
ATRX in-frame fusion neuroblastoma (patient SJNBL047443)
treatment
none (untreated)
chip antibody
none
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Tissue was homogenized at 17000 rpm for 30 seconds with a tissue homogenizer (Polytron, PT10-35GT). XL-ChIP. Libaries were prepared at Active Motif.
Sequencing Platform
instrument_model
Illumina HiSeq 2500
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
35461133
Reads aligned (%)
97.9
Duplicates removed (%)
0.5
Number of peaks
797 (qval < 1E-05)
hg19
Number of total reads
35461133
Reads aligned (%)
97.1
Duplicates removed (%)
0.6
Number of peaks
986 (qval < 1E-05)
Base call quality data from
DBCLS SRA