Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01563
Species: Homo sapiens
Position : chr20:49345710-49345732
Year: 2025
Title: Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndrome
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Normal
Disease Name: --
PMID:  40208226
MONDO:
Tissue: Heart
Tissue Ontology ID: UBERON:0000948
Cell Source: AC16 cardiomyocytes
CVCL ID: CVCL_4U18
Cell Type: cardiomyocyte
Cell Ontology ID: CL:0000746
Experiment Type: Enhancer activity assay
High Throughput Method: WGS, RNA-seq, ATAC-seq
Low Throughput Method: Luciferase reporter assay, CRISPRa, ChIP-RT-qPCR
About Target Gene
Target gene : KCNB1
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 (hg38) 1 found
Enhancer ID Position Tissue Cell Disease
E_01347 chr20:49345311-49346146 Heart cardiomyocyte --
Expression of Target Genes for the Enhancer