Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00033
Species: Homo sapiens
Position : chr8:209981000-209990000
Year: 2016
Title: Systematic mapping of functional enhancer-promoter connections with CRISPR interference
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: Acute myeloid leukemia
PMID:  27708057
MONDO: MONDO:0018874
Tissue: Bone marrow
Tissue Ontology ID: UBERON:0002371
Cell Source: K562
CVCL ID: CVCL_0004
Cell Type: Human erythroleukemia cell line
Cell Ontology ID: CL:0009084
Experiment Type: CRISPRi interference, clonal genomic deletion, Hi-C chromatin contact validation
High Throughput Method: DNase-seq, H3K27ac ChIP-seq, RNA-seq, Pol II ChIA-PET, Hi-C
Low Throughput Method: RT-qPCR, clonal cell line generation, sgRNA lentiviral transduction, cell viability assay
About Target Gene
Target gene : MYC
About TF
TF name :
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
Enhancer Associated Network
Overlapping Enhancers (hg19) 1 found
Enhancer ID Position Tissue Cell Disease
E_00034 chr8:209981000-209990000 Bone marrow Human erythroleukemia cell line Erythroleukemia
Expression of Target Genes for the Enhancer