Enhancer Detail

Comprehensive information about experimentally validated enhancers

About Enhancer
Enhancer ID: E_00795
Species: Homo sapiens
Position : chr21:36189300-36189537
Year: 2015
Title: Identification and functional analysis of acute myeloid leukemia susceptibility associated SNPs at non protein coding regions of RUNX1
Genome Build: hg19
Enhancer Type: Enhancer
Condition: Disease
Disease Name: chronic myeloid leukemia
PMID:  26656844
MONDO: MONDO:0011998
Tissue: Bone Marrow
Tissue Ontology ID: UBERON:0002371
Cell Source: K562 cell line
CVCL ID: CVCL_0004
Cell Type: chronic myeloid leukemia cell
Cell Ontology ID: CL:0001054
Experiment Type: Enhancer prediction, SNP association, Functional validation
High Throughput Method: ENCODE ChIP-seq dataset analysis, UCSC genome browser regulatory annotation
Low Throughput Method: MALDI-TOF mass spectrometry SNP genotyping
About Target Gene
Target gene : RUNX1
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_00794 chr21:36189300-36189537 Bone Marrow hematopoietic stem cell --
Expression of Target Genes for the Enhancer