Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_01522
Species: Homo sapiens
Position : chr18:70411815-70460159
Year: 2022
Title: The Tumor Invasion Paradox in Cancer Stem Cell-Driven Solid Tumors
Genome Build: hg38
Enhancer Type: Enhancer
Condition: Disease
Disease Name: acute myeloid leukemia
PMID:  36301402
MONDO: MONDO:0018874
Tissue: Bone marrow
Tissue Ontology ID: UBERON:0002371
Cell Source: Kasumi-1
CVCL ID: CVCL_0589
Cell Type: acute myeloid leukemia cell
Cell Ontology ID: CL:0001054
Experiment Type: Chromatin interaction assay, Functional perturbation assay
High Throughput Method: Hi-C, 4C-seq, CUT&Tag, RNA-seq
Low Throughput Method: CRISPR Knockout, DNA FISH, RT-RT-qPCR
About Target Gene
Target gene : RTTN
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 (hg38)
No overlapping enhancers found in hg38 at this locus.
Expression of Target Genes for the Enhancer