Variant report

Variant rs6478042
Chromosome Location chr9:116636243-116636244
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116634400-116637800 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr9:116635200-116636600 Enhancers HMEC breast
3 chr9:116635400-116637800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
4 chr9:116635400-116637800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr9:116635600-116636600 Enhancers H9 Cell Line embryonic stem cell
6 chr9:116635600-116636600 Enhancers HUES6 Cell Line embryonic stem cell
7 chr9:116635600-116636600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr9:116635800-116636400 Bivalent Enhancer H1 Cell Line embryonic stem cell
9 chr9:116635800-116636600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr9:116635800-116637600 Weak transcription NHEK skin
11 chr9:116636000-116636600 Enhancers HUES48 Cell Line embryonic stem cell
12 chr9:116636000-116637600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr9:116636000-116637800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr9:116636000-116638000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr9:116636200-116636600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr9:116636200-116637600 Weak transcription ES-I3 Cell Line embryonic stem cell

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