Variant report

Variant rs1018227
Chromosome Location chr11:108904551-108904552
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:108901000-108908800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr11:108901800-108904800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:108902000-108904600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr11:108902200-108904600 Weak transcription NHEK skin
5 chr11:108902600-108905800 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr11:108903400-108904600 Enhancers NH-A brain
7 chr11:108903600-108904600 Weak transcription HUVEC blood vessel
8 chr11:108903800-108904800 Enhancers Osteobl bone
9 chr11:108904000-108904800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr11:108904000-108906000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr11:108904200-108905400 Flanking Active TSS Muscle Satellite Cultured Cells --
12 chr11:108904400-108905600 Enhancers HMEC breast

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