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For hg38
BigWig
Peak-call (q < 1E-05)
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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)
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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: hESC derived ectodermal cells
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX3481055
GSM2893678: AP2Cd7Off 2; Homo sapiens; ATAC-seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
ATAC-Seq
Antigen
ATAC-Seq
Cell type
Cell type Class
Pluripotent stem cell
Cell type
hESC derived ectodermal cells
NA
NA
Attributes by original data submitter
Sample
source_name
early surface ectoderm differentiation from hESC
originating cell line
H9
cell type
control ES without specific differentiation
genotype/variation
TetO-TFAP2C
treatment and stage
Dox- for 7 days
Sequenced DNA Library
library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Around 50,000 cells were used for each transposition reaction. Nuclei were prepared prior to transposition. Sequencing libraries were constructed using a modified version of the Illumina Nextera DNA Sample prep kit.
Sequencing Platform
instrument_model
NextSeq 500
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
84778585
Reads aligned (%)
68.2
Duplicates removed (%)
25.8
Number of peaks
9774 (qval < 1E-05)
hg19
Number of total reads
84778585
Reads aligned (%)
67.8
Duplicates removed (%)
26.1
Number of peaks
9366 (qval < 1E-05)
Base call quality data from
DBCLS SRA