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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: LX2
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX148893
GSM934613: input; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Liver
Cell type
LX2
NA
NA
Attributes by original data submitter
Sample
source_name
human LX2 cells
cell type
human hepatic stellate cells
cell line
LX2
chip antibody
none
treatment
none
Sequenced DNA Library
library_name
GSM934613: input
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
37172791
Reads aligned (%)
94.9
Duplicates removed (%)
17.2
Number of peaks
1307 (qval < 1E-05)
hg19
Number of total reads
37172791
Reads aligned (%)
93.9
Duplicates removed (%)
19.0
Number of peaks
1308 (qval < 1E-05)
Base call quality data from
DBCLS SRA