Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_03915
Species: Homo sapiens
Position : chr2:60494251-60495546
Year: 2020
Title: Therapeutic base editing of human hematopoietic stem cells.
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Disease
Disease Name: beta-thalassemia
PMID:  32284612
MONDO: MONDO:0019402
Tissue: blood
Tissue Ontology ID: UBERON:0000178
Cell Source: CD34+ hematopoietic stem and progenitor cells
Cell Type: hematopoietic stem cell
Cell Ontology ID: CL:0000037
Experiment Type: Functional perturbation assay; enhancer editing assay; Disease-variant functional analysis; In vivo functional validation
High Throughput Method: Amplicon deep sequencing; Illumina sequencing
Low Throughput Method: CRISPR base editing; RT-qPCR; HbF measurement; HPLC; erythroid differentiation assay; In vivo phenotyping
About Target Gene
Target gene : BCL11A
About TF
TF name : TAL1
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
Enhancer Associated Network
Overlapping Enhancers (hg38) 3 found
Enhancer ID Position Tissue Cell Disease
E_03912 chr2:60494251-60495546 blood hematopoietic stem cell sickle cell disease
E_03913 chr2:60494251-60495546 blood hematopoietic stem cell beta-thalassemia
E_03914 chr2:60494251-60495546 blood hematopoietic stem cell sickle cell disease
Expression of Target Genes for the Enhancer