Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_04997
Species: Homo sapiens
Position : chr10:33492690-33519530
Year: 2018
Title: Mutant p63 Affects Epidermal Cell Identity through Rewiring the Enhancer Landscape.
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: EEC syndrome
PMID:  30566872
Cell Source: Normal Epidermal Cell
Experiment Type: TF-binding/chromatin assay; Disease-associated enhancer analysis
High Throughput Method: ChIP-seq
Low Throughput Method: ChIP-qPCR/ChIP; RT-qPCR/qPCR; RNAi/siRNA/shRNA
About Target Gene
Target gene : NRP1
About TF
TF name : RUNX1
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
RUNX1 AndrogenReceptor netpath 167
RUNX1 Organic cation transport reactome 9
RUNX1 RANKL netpath 84
RUNX1 Regulation of nuclear SMAD2/3 signaling pid 82
RUNX1 TGF_beta_Receptor netpath 220
RUNX1 Validated transcriptional targets of deltaNp63 isoforms pid 47
RUNX1 Pathways in cancer kegg 321
RUNX1 Chronic myeloid leukemia kegg 69
RUNX1 Acute myeloid leukemia kegg 53
Enhancer Associated Network
Overlapping Enhancers (hg19) 3 found
Enhancer ID Position Tissue Cell Disease
E_04998 chr10:33492690-33519530 NA NA EEC syndrome
E_04999 chr10:33512793-33539633 NA NA EEC syndrome
E_05000 chr10:33512793-33539633 NA NA EEC syndrome
Expression of Target Genes for the Enhancer