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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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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: ATAC-Seq
wikigenes
PDBj
CellType: EndoC-BH1
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX5099789
GSM3502704: EndoC-βH1 control rep 2; Homo sapiens; ATAC-seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
ATAC-Seq
Antigen
ATAC-Seq
Cell type
Cell type Class
Pancreas
Cell type
EndoC-BH1
NA
NA
Attributes by original data submitter
Sample
source_name
EndoC-βH1
treatment
Control
cell type
EndoC-[beta]H1
Sequenced DNA Library
library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Nuclei from 50,000 cells were isolated and then lysed to extract DNA. ATAC-seq libraries were prepared using standard Illumina protocols
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
108217593
Reads aligned (%)
85.3
Duplicates removed (%)
62.0
Number of peaks
44049 (qval < 1E-05)
hg19
Number of total reads
108217593
Reads aligned (%)
85.1
Duplicates removed (%)
62.6
Number of peaks
43718 (qval < 1E-05)
Base call quality data from
DBCLS SRA