Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00602
Species: Homo sapiens
Position : chr13:28268000-28270000
Year: 2022
Title: Concurrent CDX2 cis-deregulation and UBTF::ATXN7L3 fusion define a novel high-risk subtype of B-cell ALL
Genome Build: hg19
Enhancer Type: Promoter
Condition: Disease
Disease Name: B-cell acute lymphoblastic leukemia
PMID:  35316324
MONDO: MONDO:0004945
Tissue: Bone Marrow
Tissue Ontology ID: UBERON:0002371
Cell Source: PDX B-ALL cells
CVCL ID:
Cell Type: patient-derived xenograft B-ALL cell
Cell Ontology ID: CL:0000945
Experiment Type: Histone modification ChIP-seq, Chromosome conformation capture sequencing, RNA-DNA FISH
High Throughput Method: H3K27ac ChIP-seq, H3K4me3 ChIP-seq, 4C-seq, RNA-seq
Low Throughput Method: Allele-specific expression analysis
About Target Gene
Target gene : CDX2
About TF
TF name : CDX2
About Regulatory State
Regulatory State : Active
Upstream Pathway Annotation of TF
GeneName Pathway Name Source Gene Number
CDX2 POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation reactome 10
CDX2 Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) reactome 20
Enhancer Associated Network
Overlapping Enhancers (hg19) 2 found
Enhancer ID Position Tissue Cell Disease
E_00603 chr13:28268000-28270000 Bone Marrow B lymphoblast B-cell acute lymphoblastic leukemia
E_00604 chr13:28268000-28270000 Bone Marrow B lymphoblast B-cell acute lymphoblastic leukemia
Expression of Target Genes for the Enhancer