Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_03894
Species: Homo sapiens
Position : chr10:81115805-81116305
Year: 2021
Title: Genome-wide enhancer maps link risk variants to disease genes.
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: inflammatory bowel disease
PMID:  33828297
MONDO: MONDO:0005265
Tissue: blood
Tissue Ontology ID: UBERON:0000178
Cell Source: THP-1
CVCL ID: CVCL_0006
Cell Type: monocyte
Cell Ontology ID: CL:0000576
Experiment Type: Enhancer-target functional validation; endogenous perturbation; downstream cellular phenotype; Disease-variant functional analysis
High Throughput Method: ATAC-seq/DNase-seq; H3K27ac profiling; Hi-C; ABC enhancer-gene mapping; GWAS
Low Throughput Method: CRISPRi-FlowFISH; PPIF expression analysis; MitoTracker mitochondrial membrane-potential assay
About Target Gene
Target gene : PPIF
About TF
TF name : NA
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
Enhancer Associated Network
Overlapping Enhancers (hg19)
No overlapping enhancers found in hg19 at this locus.
Expression of Target Genes for the Enhancer