The 2.0 version of rSNPBase

Variant report

Variant rs698573
Chromosome Location chr2:189674561-189674562
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:189668600-189675400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:189672800-189678400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr2:189673000-189674600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
4 chr2:189673000-189675400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr2:189673000-189676800 Enhancers NHDF-Ad bronchial
6 chr2:189673000-189678400 Enhancers Osteobl bone
7 chr2:189673200-189674800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr2:189673800-189677600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr2:189674200-189675600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr2:189674200-189676000 Weak transcription NH-A brain
11 chr2:189674400-189675400 Weak transcription Muscle Satellite Cultured Cells --
12 chr2:189674400-189676000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr2:189674400-189676000 Weak transcription NHLF lung

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Last update: Aug 31, 2015