Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00796
Species: Homo sapiens
Position : chr16:1480850-1482378
Year: 2019
Title: Noncoding deletions reveal a gene that is critical for intestinal function
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Normal
Disease Name: --
PMID:  31217582
MONDO:
Tissue: Gastrointestinal Tract
Tissue Ontology ID: UBERON:0000160
Cell Source: Enteroendocrine cells
CVCL ID:
Cell Type: enteroendocrine cell
Cell Ontology ID: CL:0000164
Experiment Type: Functional perturbation assay
High Throughput Method: WGS, WES, RNA-seq
Low Throughput Method: CRISPR Knockout, RT-RT-qPCR, Western blot, Immunofluorescence
About Target Gene
Target gene : PERCC1
About TF
TF name :
About Regulatory State
Regulatory State : Silenced
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_00509 chr16:1480850-1482378 Stomach gastrointestinal epithelial cell --
Expression of Target Genes for the Enhancer