The 2.0 version of rSNPBase

Variant report

Variant rs6784356
Chromosome Location chr3:100908969-100908970
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100901800-100911800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr3:100903000-100912800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr3:100904600-100914600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr3:100907400-100912400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr3:100908000-100909800 Enhancers Muscle Satellite Cultured Cells --
6 chr3:100908000-100909800 Enhancers Osteobl bone
7 chr3:100908400-100909200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr3:100908400-100910400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr3:100908400-100911600 Enhancers NHDF-Ad bronchial
10 chr3:100908600-100909600 Enhancers NHLF lung
11 chr3:100908600-100910000 Enhancers A549 lung
12 chr3:100908600-100911600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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Last update: Aug 31, 2015