Toggle navigation
Peak Browser
Enrichment Analysis
Diff Analysis
Target Genes
Colocalization
Publications
Docs
Search
Go
Find By ID
Visualize
Install and launch IGV before selecting data to visualize
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For mm10
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For mm9
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
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: Intestinal epithelium
ATCC
MeSH
RIKEN BRC
SRX5862978
GSM3780706: Sox9 Negative atac Rep C; Mus musculus; ATAC-seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
ATAC-Seq
Antigen
ATAC-Seq
Cell type
Cell type Class
Digestive tract
Cell type
Intestinal epithelium
NA
NA
Attributes by original data submitter
Sample
source_name
Intestinal epithelial cells
strain
C57BL/6
cell type
Intestinal epithelial cells
cell population
Sox9 Negative
Sequenced DNA Library
library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
12,000 cells per Sox9EGFP population were collected directly into 250uL 1X sort media, pelleted by centrifugation at 2,000g for 5min, and subjected to Omni-ATAC as previously described in (Corces et al., 2017). Paired end omni-atac protocol
Sequencing Platform
instrument_model
NextSeq 500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
67249045
Reads aligned (%)
62.5
Duplicates removed (%)
34.9
Number of peaks
38250 (qval < 1E-05)
mm9
Number of total reads
67249045
Reads aligned (%)
62.4
Duplicates removed (%)
35.0
Number of peaks
38197 (qval < 1E-05)
Base call quality data from
DBCLS SRA