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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)
Error connecting to IGV?
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: NA
wikigenes
PDBj
CellType: Polymorphonuclear leukocytes
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX1016679
chip-seq of individual exposed to high pm2.5 rep 1 (CHIP)
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
No description
Antigen
NA
Cell type
Cell type Class
Blood
Cell type
Polymorphonuclear leukocytes
NA
NA
Attributes by original data submitter
Sample
isolate
PM2.5_high_1
age
>18
biomaterial_provider
Wei Zhang
sex
not collected
tissue
polymorphonuclear leukocytes
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
24223516
Reads aligned (%)
42.3
Duplicates removed (%)
19.6
Number of peaks
6603 (qval < 1E-05)
hg19
Number of total reads
24223516
Reads aligned (%)
41.9
Duplicates removed (%)
19.9
Number of peaks
6473 (qval < 1E-05)
Base call quality data from
DBCLS SRA