Comprehensive information about experimentally validated enhancers
| Enhancer ID: | E_04580 |
| Species: | Homo sapiens |
| Position : | chr5:110175800-110176600 |
| Year: | 2016 |
| Title: | Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. |
| Genome Build: | hg19 |
| Enhancer Type: | Enhancer |
| Condition: | Disease |
| Disease Name: | Heart Failure |
| PMID: | 27149122 |
| Tissue: | heart |
| Tissue Ontology ID: | UBERON:0000948 |
| Cell Source: | 293T |
| CVCL ID: | CVCL_0063 |
| Experiment Type: | Enhancer activity assay; Genetic-variant functional analysis; Disease-associated enhancer analysis |
| Low Throughput Method: | Luciferase reporter assay; Reporter assay |
| Target gene : | TSLP |
| TF name : | NA |
| Regulatory State : | Active |
| GeneName | Pathway Name | Source | Gene Number |
|---|
| Enhancer ID | Position | Tissue | Cell | Disease |
|---|---|---|---|---|
| E_04563 | chr5:110175120-110177136 | heart | NA | Heart Failure |