Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01626
Species: Homo sapiens
Position : chr9:94190762-94191795
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 adipogenic differentiation
Cell Type: adipocyte
Cell Ontology ID: CL:0000136
Experiment Type: Super-enhancer constituent activity 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 NFIL3-SE functional region FR3; RT-qPCR; Nile red staining
About Target Gene
Target gene : NFIL3
About TF
TF name : NA
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