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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: KNS-42
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
DRX223746
Illumina NovaSeq 6000 paired end sequencing of SAMD00231553
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Neural
Cell type
KNS-42
Primary Tissue
Brain
Tissue Diagnosis
Glioma
Attributes by original data submitter
Sample
sample_name
KNS-42_G34V_delta1_Input
biomaterial_provider
JCRB cell bank
cell_line
KNS-42
cell_type
glioma
genotype
G34V knocked out
technical_replicate
1
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
SMARTer ThruPLEX DNA-seq Kit (Takara Bio)
Sequencing Platform
instrument_model
Illumina NovaSeq 6000
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
28124296
Reads aligned (%)
78.3
Duplicates removed (%)
4.2
Number of peaks
481 (qval < 1E-05)
hg19
Number of total reads
28124296
Reads aligned (%)
77.7
Duplicates removed (%)
4.3
Number of peaks
218 (qval < 1E-05)
Base call quality data from
DBCLS SRA