Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_02804
Species: Homo sapiens
Position : chr12:114463712-114464080
Year: 2012
Title: Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: Congenital Heart Disease
PMID:  22543974
Tissue: heart
Tissue Ontology ID: UBERON:0000948
Cell Source: HeLa
CVCL ID: CVCL_0030
Cell Type: malignant cell
Cell Ontology ID: CL:0001064
Experiment Type: TF-binding/chromatin assay; Genetic-variant functional analysis; In vivo functional validation; Disease-associated enhancer analysis
High Throughput Method: ChIP-seq
Low Throughput Method: ChIP-qPCR/ChIP; EMSA/gel-shift assay
About Target Gene
Target gene : TBX5
About TF
TF name : TBX5
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
TBX5 Physiological factors reactome 12
TBX5 YAP1- and WWTR1 (TAZ)-stimulated gene expression reactome 29
TBX5 Hs_Heart_Development_WP1591_90186 wikipathways 28
Enhancer Associated Network
Overlapping Enhancers (hg19) 2 found
Enhancer ID Position Tissue Cell Disease
E_02808 chr12:114463712-114464080 heart NA Congenital Heart Disease
E_02911 chr12:114463712-114464080 blood B lymphoblastoid cell NA
Expression of Target Genes for the Enhancer