Comprehensive information about experimentally validated enhancers
| 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 |
| Target gene : | AMOTL2 |
| TF name : | NA |
| Regulatory State : | Active |
| GeneName | Pathway Name | Source | Gene Number |
|---|
| Enhancer ID | Position | Tissue | Cell | Disease |
|---|---|---|---|---|
| E_01696 | chr3:134460112-134466940 | coronary artery | smooth muscle cell of the coronary artery | coronary artery disorder |