About Enhancer
| Enhancer ID: | E_01674 |
| Species: | Homo sapiens |
| Position : | chr3:171555500-171556000   |
| 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:0001621 |
| Cell Source: | HCASMC |
| CVCL ID: | |
| Cell Type: | coronary artery smooth muscle cell |
| Cell Ontology ID: | CL:0000192 |
| Experiment Type: | Chromatin interaction assay, Functional perturbation assay |
| High Throughput Method: | HiChIP, ATAC-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