Variant report

Variant rs56207699
Chromosome Location chr4:166375409-166375410
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:166362200-166381600 Weak transcription Fetal Stomach stomach
2 chr4:166362400-166381600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr4:166362400-166382400 Weak transcription Aorta Aorta
4 chr4:166362400-166384600 Weak transcription Brain Cingulate Gyrus brain
5 chr4:166362600-166379000 Weak transcription Fetal Brain Female brain
6 chr4:166362800-166379200 Weak transcription Brain Anterior Caudate brain
7 chr4:166372400-166379000 Weak transcription Fetal Brain Male brain
8 chr4:166374800-166376000 Enhancers HepG2 liver
9 chr4:166375000-166376000 Active TSS Pancreatic Islets Pancreatic Islet
10 chr4:166375000-166376200 Enhancers HMEC breast
11 chr4:166375200-166376400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr4:166375200-166376400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links