Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01402
Species: Homo sapiens
Position : chr3:134200000-134500000
Year: 2024
Title: Single cell variant to enhancer to gene map for coronary artery disease
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Normal
Disease Name: --
PMID:  39606421
MONDO:
Tissue: Artery
Tissue Ontology ID: UBERON:0001628
Cell Source: Human Coronary Artery Smooth Muscle Cells (HCASMC)
CVCL ID:
Cell Type: coronary artery smooth muscle cell
Cell Ontology ID: CL:0000192
Experiment Type: Functional validation, Chromatin interaction
High Throughput Method: Hi-C, HiChIP-seq, ATAC-seq, ChIP-seq, RNA-seq
Low Throughput Method: CRISPRi, RT-RT-qPCR
About Target Gene
Target gene : AMOTL2
About TF
TF name :
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
Enhancer Associated Network
Overlapping Enhancers (hg38)
No overlapping enhancers found in hg38 at this locus.
Expression of Target Genes for the Enhancer