Variant report

Variant rs1018228
Chromosome Location chr11:108904140-108904141
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:108899000-108904200 Weak transcription Muscle Satellite Cultured Cells --
2 chr11:108901000-108908800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr11:108901800-108904800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:108902000-108904400 Weak transcription HMEC breast
5 chr11:108902000-108904600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr11:108902200-108904600 Weak transcription NHEK skin
7 chr11:108902600-108905800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr11:108903400-108904600 Enhancers NH-A brain
9 chr11:108903600-108904600 Weak transcription HUVEC blood vessel
10 chr11:108903800-108904800 Enhancers Osteobl bone
11 chr11:108904000-108904800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr11:108904000-108906000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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