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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: BE(2)-C
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX111319
GSM848787: Input; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Neural
Cell type
BE(2)-C
Primary Tissue
Brain
Site of Extraction
Bone Marrow
Tissue Diagnosis
Neuroblastoma
Attributes by original data submitter
Sample
source_name
BE2C/Tet-Off/HOXC9_Doxy-_6d_Input
cell line
BE(2)-C/Tet-Off/Myc-HOXC9
tumor cell type
Neuroblastoma
chip antibody
None
tissue origin
Sympathetic nervous system
Sequenced DNA Library
library_name
GSM848787: Input
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer IIx
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
41735085
Reads aligned (%)
92.9
Duplicates removed (%)
23.4
Number of peaks
1399 (qval < 1E-05)
hg19
Number of total reads
41735085
Reads aligned (%)
91.9
Duplicates removed (%)
24.6
Number of peaks
1261 (qval < 1E-05)
Base call quality data from
DBCLS SRA