Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01459
Species: Homo sapiens
Position : chr3:36999364-37001216
Year: 2018
Title: Disruption of a -35 kb Enhancer Impairs CTCF Binding and MLH1 Expression in Colorectal Cells.
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: Lynch Syndrome
PMID:  29898989
Tissue: colon
Tissue Ontology ID: UBERON:0001155
Cell Source: SW620,RKO
Experiment Type: Enhancer activity assay; TF-binding/chromatin assay; Chromatin interaction assay; Endogenous enhancer perturbation; Disease-associated enhancer analysis
Low Throughput Method: Luciferase reporter assay; Reporter assay; CRISPR-Cas9 targeted editing/deletion; ChIP-qPCR/ChIP; 3C; RT-qPCR/qPCR
About Target Gene
Target gene : MLH1
About TF
TF name : CTCF
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
CTCF Activation of anterior HOX genes in hindbrain development during early embryogenesis reactome 120
CTCF TGF_beta_Receptor netpath 220
Enhancer Associated Network
Overlapping Enhancers (hg19) 1 found
Enhancer ID Position Tissue Cell Disease
E_01448 chr3:36999364-37001216 colon malignant cell colorectal carcinoma
Expression of Target Genes for the Enhancer