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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: RAD21
wikigenes
PDBj
CellType: HAP1
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX15337400
GSM6167095: YL-NBS1-CTCF-R8; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
RAD21
Cell type
Cell type Class
Blood
Cell type
HAP1
NA
NA
Attributes by original data submitter
Sample
source_name
HAP1-RAD21-TEV cells
protocol
Hi-C 2.0
enzyme
DpnII
cell line
HAP1-RAD21-TEV cells
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Nuclei were purified using hytonic buffer and after treatments, nuclei were fixed for Hi-C protocol ChIPseq (PMID31522987)
Sequencing Platform
instrument_model
Illumina HiSeq 4000
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
34649368
Reads aligned (%)
77.7
Duplicates removed (%)
34.6
Number of peaks
21678 (qval < 1E-05)
hg19
Number of total reads
34649368
Reads aligned (%)
77.0
Duplicates removed (%)
35.1
Number of peaks
21448 (qval < 1E-05)
Base call quality data from
DBCLS SRA