Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01852
Species: Homo sapiens
Position : chr4:111399594-111399691
Year: 2024
Title: Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Disease
Disease Name: hepatocellular carcinoma
PMID:  38592784
MONDO: MONDO:0007256
Tissue: Liver
Tissue Ontology ID: UBERON:0002107
Cell Source: HepG2
CVCL ID: CVCL_0027
Cell Type: hepatocellular carcinoma cell
Cell Ontology ID: CL:0000182
Experiment Type: TF binding assay, Functional perturbation assay
High Throughput Method: RNA-seq
Low Throughput Method: ChIP-RT-qPCR, RT-RT-qPCR, Western blot
About Target Gene
Target gene : PITX2
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) 2 found
Enhancer ID Position Tissue Cell Disease
E_01586 chr4:111397892-111402926 Embryonic Kidney embryonic kidney cell --
E_01587 chr4:111397892-111402926 Sclera scleral fibroblast --
Expression of Target Genes for the Enhancer