Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_04672
Species: Homo sapiens
Position : chrX:135990759-135994160
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
PMID:  39272130
Tissue: blood
Tissue Ontology ID: UBERON:0000178
Cell Source: PBMCs
Cell Type: peripheral blood mononuclear cell
Cell Ontology ID: CL:2000001
Experiment Type: Chromatin interaction assay; Disease-variant functional analysis
High Throughput Method: Hi-C, 4C-seq; 4C-seq
Low Throughput Method: qRT-PCR, and ChIP-qPCR; 4C
About Target Gene
Target gene : GPR101
About TF
TF name : NA
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_04603 chrX:135990759-135994160 blood peripheral blood mononuclear cell NA
Expression of Target Genes for the Enhancer