Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00932
Species: Homo sapiens
Position : chrX:135656769-135660247
Year: 2024
Title: Chromatin conformation capture in the clinic: 4C-seq/HiC distinguishes pathogenic from neutral duplications at the GPR101 locus
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Normal
Disease Name: --
PMID:  39272130
MONDO:
Tissue: Peripheral Blood
Tissue Ontology ID: UBERON:0000178
Cell Source: PBMCs
CVCL ID:
Cell Type: peripheral blood mononuclear cell
Cell Ontology ID: CL:0000738
Experiment Type: Chromatin interaction assay
High Throughput Method: Hi-C, 4C-seq
Low Throughput Method: qRT-PCR, and ChIP-qPCR
About Target Gene
Target gene : GPR101
About TF
TF name :
About Regulatory State
Regulatory State : Active
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_00783 chrX:135656769-135660247 Peripheral Blood peripheral blood mononuclear cell --
Expression of Target Genes for the Enhancer