Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_03944
Species: Homo sapiens
Position : chr1:178551259-178551689
Year: 2025
Title: Genetic effects on chromatin accessibility uncover mechanisms of liver gene regulation and quantitative traits.
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Normal
PMID:  40393811
Tissue: bone marrow
Tissue Ontology ID: UBERON:0002371
Cell Source: Adipose-Derived Mesenchymal Stem Cells-01
Cell Type: mesenchymal stem cell
Cell Ontology ID: CL:0000134
Experiment Type: Enhancer activity assay, Functional perturbation assay; Endogenous enhancer perturbation; Disease-variant functional analysis
High Throughput Method: ATAC-seq, RNA-seq; eQTL analysis; GWAS
Low Throughput Method: Luciferase Reporter Assay, CRISPR Knockout, CRISPRi, RT-RT-qPCR; CRISPRi
About Target Gene
Target gene : RALGPS2
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)
No overlapping enhancers found in hg38 at this locus.
Expression of Target Genes for the Enhancer