Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00904
Species: Homo sapiens
Position : chr8:128018000-128023000
Year: 2020
Title: A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer.
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Disease
Disease Name: prostate cancer
PMID:  32680982
MONDO: MONDO:0008315
Tissue: prostate gland
Tissue Ontology ID: UBERON:0002367
Cell Source: LNCaP clone FGC
CVCL ID: CVCL_1379
Cell Type: malignant cell
Cell Ontology ID: CL:0001064
Experiment Type: Enhancer activity assay; TF binding assay; Chromatin interaction assay; Functional perturbation assay; Disease-variant functional analysis
High Throughput Method: AR ChIP-seq; FOXA1 ChIP-seq; H3K27ac ChIP-seq; ATAC-seq; DHS; 4C
Low Throughput Method: Allele-specific Luciferase reporter assay; EMSA; SPDEF knockdown; CRISPRi; RT-qPCR
About Target Gene
Target gene : MYC
About TF
TF name : SPDEF
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
SPDEF AndrogenReceptor netpath 167
SPDEF PDGF signaling pathway panther 113
SPDEF Regulation of Androgen receptor activity pid 54
Enhancer Associated Network
Overlapping Enhancers (hg38) 3 found
Enhancer ID Position Tissue Cell Disease
E_03876 chr8:126650000-129950000 colon malignant cell NA
E_00903 chr8:128018000-128023000 prostate gland malignant cell prostate cancer
E_00905 chr8:128018000-128023000 prostate gland malignant cell prostate cancer
Expression of Target Genes for the Enhancer