Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_03896
Species: Homo sapiens
Position : chr1:199217982-199218479
Year: 2020
Title: Cancer-specific CTCF binding facilitates oncogenic transcriptional dysregulation.
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Disease
Disease Name: T-cell acute lymphoblastic leukemia
PMID:  32933554
MONDO: MONDO:0004963
Tissue: blood
Tissue Ontology ID: UBERON:0000178
Cell Source: CUTLL1
CVCL ID: CVCL_4966
Cell Type: malignant cell
Cell Ontology ID: CL:0001064
Experiment Type: TF binding assay; Chromatin interaction assay; Chromatin accessibility profiling; Cancer-specific regulatory-site characterization
High Throughput Method: CTCF ChIP-seq; ATAC-seq; in situ Hi-C; RNA-seq; WGS; DNA methylation profiling
Low Throughput Method: ChIP-qPCR; RT-qPCR; Western blot; NOTCH1-pathway perturbation/validation
About Target Gene
Target gene : NA
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 (hg38)
No overlapping enhancers found in hg38 at this locus.
Expression of Target Genes for the Enhancer