Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01025
Species: Homo sapiens
Position : chr16:155136-155210
Year: 2025
Title: An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the ??-globin regulatory elements and ??-thalassemia-SEA deletion
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: T-cell acute lymphoblastic leukemia
PMID:  39934429
MONDO: MONDO:0004947
Tissue: Blood
Tissue Ontology ID: UBERON:0000178
Cell Source: Leukemic T Lymphoblasts
CVCL ID:
Cell Type: T lymphoblast
Cell Ontology ID: CL:0002419
Experiment Type: Functional perturbation assay
High Throughput Method: ATAC-seq
Low Throughput Method: qRT-PCR, and ChIP-qPCR
About Target Gene
Target gene : HBA1
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 (hg19)
No overlapping enhancers found in hg19 at this locus.
Expression of Target Genes for the Enhancer