Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00269
Species: Homo sapiens
Position : chr11:1713879-1716230
Year: 2021
Title: Large parental differences in chromatin organization in pancreatic beta cell line explaining diabetes susceptibility effects
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Normal
Disease Name: --
PMID:  34267199
MONDO:
Tissue: Pancreatic islet
Tissue Ontology ID: UBERON:0000006
Cell Source: primary human pancreatic islets
CVCL ID:
Cell Type: pancreatic islet cell
Cell Ontology ID: CL:0000168
Experiment Type: Enhancer activity assay, Chromatin interaction assay, Functional perturbation assay
High Throughput Method: 3C-seq, 4C-seq, ChIP-seq, RNA-seq, ATAC-seq
Low Throughput Method: CRISPR Knockout, RT-RT-qPCR, EMSA, Sanger Sequencing
About Target Gene
Target gene : INS
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_00270 chr11:1713879-1716230 Cranial neural crest cranial neural crest cell --
Expression of Target Genes for the Enhancer