Variant report

Variant rs193091553
Chromosome Location chr9:116590558-116590559
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116585000-116590800 Weak transcription Aorta Aorta
2 chr9:116590200-116590600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr9:116590200-116591000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr9:116590400-116590600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr9:116590400-116590600 Flanking Active TSS Muscle Satellite Cultured Cells --
6 chr9:116590400-116590600 Flanking Active TSS Osteobl bone
7 chr9:116590400-116591000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr9:116590400-116591000 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr9:116590400-116591000 Flanking Active TSS HUVEC blood vessel
10 chr9:116590400-116591000 Enhancers NH-A brain
11 chr9:116590400-116591000 Active TSS NHLF lung

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