Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01586
Species: Homo sapiens
Position : chr4:111397892-111402926
Year: 2024
Title: Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Normal
Disease Name: --
PMID:  38592784
MONDO:
Tissue: Embryonic Kidney
Tissue Ontology ID: UBERON:0002113
Cell Source: HEK293
CVCL ID: CVCL_0045
Cell Type: embryonic kidney cell
Cell Ontology ID: CL:0002139
Experiment Type: Enhancer activity assay, Functional perturbation assay, TF binding assay
High Throughput Method: ChIP-seq, RNA-seq
Low Throughput Method: CRISPR Knockout, 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_01587 chr4:111397892-111402926 Sclera scleral fibroblast --
E_01852 chr4:111399594-111399691 Liver hepatocellular carcinoma cell hepatocellular carcinoma
Expression of Target Genes for the Enhancer