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 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: TFAP4
wikigenes
PDBj
CellType: SNU-1750
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX1892834
GSM2224583: SNU175 TFAP4; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
TFAP4
Cell type
Cell type Class
Digestive tract
Cell type
SNU-1750
NA
NA
Attributes by original data submitter
Sample
source_name
Colorectal cancer cell line
cell line
SNU175
cell type
Colorectal cancer cell line
genetic modification
none
library strategy
transcription factor ChIP-seq
chip antibody
anti-TFAP4 (Santa Cruz Biotechnology, sc-18593X)
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Libraries were purified using QIA quick column (DNase I-seq, ATAC-seq, Targeted RNA-/DNA-seq, and 4C-seq), QIA minElute column (ChIP-seq) or SPRI beads (ATAC-seq). Libraries were prepared according to Illumina's instructions.
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
50560541
Reads aligned (%)
90.0
Duplicates removed (%)
47.2
Number of peaks
42764 (qval < 1E-05)
hg19
Number of total reads
50560541
Reads aligned (%)
89.5
Duplicates removed (%)
48.0
Number of peaks
42777 (qval < 1E-05)
Base call quality data from
DBCLS SRA