Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01613
Species: Homo sapiens
Position : chr15:99948331-99948831
Year: 2022
Title: Lineage-selective super enhancers mediate core regulatory circuitry during adipogenic and osteogenic differentiation of human mesenchymal stem cells.
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: obesity
PMID:  36224171
MONDO: MONDO:0011122
Tissue: mesenchyme of umbilical cord
Tissue Ontology ID: UBERON:0003422
Cell Source: Primary human umbilical cord-derived hMSCs after osteogenic differentiation
Cell Type: osteoblast
Cell Ontology ID: CL:0000062
Experiment Type: Super-enhancer constituent activity assay; TF binding assay; Functional enhancer perturbation assay; Lineage-specific differentiation assay; Disease-variant functional analysis
High Throughput Method: H3K27ac ChIP-seq; DNase-seq; RNA-seq; GWAS
Low Throughput Method: CRISPR-Cas9 deletion of MEF2A-SE functional region FR2; MEF2A ChIP-qPCR; RT-qPCR; ALP staining; dCas9-KRAB CRISPRi
About Target Gene
Target gene : MEF2A
About TF
TF name : MEF2A
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
MEF2A CDO in myogenesis reactome 29
MEF2A ERK/MAPK targets reactome 17
MEF2A Signaling mediated by p38-alpha and p38-beta pid 35
MEF2A TGF_beta_Receptor netpath 220
MEF2A Hs_p38_MAPK_Signaling_Pathway_WP400_72084 wikipathways 28
Enhancer Associated Network
Overlapping Enhancers (hg19) 1 found
Enhancer ID Position Tissue Cell Disease
E_01612 chr15:99948331-99948831 mesenchyme of umbilical cord osteoblast obesity
Expression of Target Genes for the Enhancer