The 2.0 version of rSNPBase

Variant report

Variant rs6589046
Chromosome Location chr11:108901856-108901857
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:108894200-108903800 Weak transcription Osteobl bone
2 chr11:108899000-108904200 Weak transcription Muscle Satellite Cultured Cells --
3 chr11:108901000-108904000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr11:108901000-108908800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr11:108901400-108902000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr11:108901600-108902000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:108901600-108902000 Enhancers HMEC breast
8 chr11:108901600-108902200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr11:108901800-108902200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr11:108901800-108902200 Enhancers NHEK skin
11 chr11:108901800-108904800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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Last update: Aug 31, 2015