Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01740
Species: Homo sapiens
Position : chr3:134460112-134466940
Year: 2024
Title: Single cell variant to enhancer to gene map for coronary artery disease.
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Disease
Disease Name: coronary artery disorder
PMID:  39606421
MONDO: MONDO:0005010
Tissue: coronary artery
Tissue Ontology ID: UBERON:0001621
Cell Source: Primary human coronary artery smooth muscle cells (HCASMC)
Cell Type: smooth muscle cell of the coronary artery
Cell Ontology ID: CL:0002592
Experiment Type: Enhancer activity assay; Chromatin interaction assay; Functional perturbation assay; Cell-type-specific enhancer validation
High Throughput Method: H3K27ac ChIP-seq; HiChIP-seq; snATAC-seq; Hi-C
Low Throughput Method: CRISPRi (dCas9-KRAB; two independent enhancer-targeting sgRNAs); RT-PCR; CRISPRi
About Target Gene
Target gene : AMOTL2
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 (hg38) 1 found
Enhancer ID Position Tissue Cell Disease
E_01696 chr3:134460112-134466940 coronary artery smooth muscle cell of the coronary artery coronary artery disorder
Expression of Target Genes for the Enhancer