Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01588
Species: Homo sapiens
Position : chr15:78750919-78751419
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: TF binding, Chromatin interaction
High Throughput Method: Hi-C, ChIP-seq, ATAC-seq, RNA-seq
Low Throughput Method: EMSA
About Target Gene
Target gene : ADAMTS7
About TF
TF name : CTCF
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
CTCF Activation of anterior HOX genes in hindbrain development during early embryogenesis reactome 120
CTCF TGF_beta_Receptor netpath 220
Enhancer Associated Network
Overlapping Enhancers (hg38)
No overlapping enhancers found in hg38 at this locus.
Expression of Target Genes for the Enhancer