Variant report

Variant rs11997155
Chromosome Location chr8:69982528-69982529
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:69979600-69985200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr8:69980200-69984600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr8:69980600-69984800 Enhancers HSMM muscle
4 chr8:69981000-69983200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr8:69981000-69983600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr8:69981200-69983400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr8:69981200-69985000 Enhancers Osteobl bone
8 chr8:69981400-69983000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr8:69981400-69983400 Enhancers NHDF-Ad bronchial
10 chr8:69982200-69983600 Enhancers NHEK skin
11 chr8:69982200-69984400 Enhancers NHLF lung
12 chr8:69982400-69983000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr8:69982400-69983200 Flanking Active TSS Muscle Satellite Cultured Cells --
14 chr8:69982400-69988200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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