Variant report

Variant rs2700672
Chromosome Location chr3:99115294-99115295
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:99105000-99116800 Weak transcription Aorta Aorta
2 chr3:99112600-99116200 Enhancers NHLF lung
3 chr3:99112600-99116400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr3:99112800-99116200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
5 chr3:99113000-99116000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr3:99113000-99116000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr3:99113200-99115400 Enhancers HSMM muscle
8 chr3:99113200-99116200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr3:99113800-99116400 Enhancers Osteobl bone
10 chr3:99114000-99116800 Enhancers NHDF-Ad bronchial
11 chr3:99114400-99115600 Enhancers HMEC breast
12 chr3:99114800-99115400 Enhancers NHEK skin
13 chr3:99115000-99115400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr3:99115000-99116000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr3:99115200-99115400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr3:99115200-99115400 Flanking Active TSS Muscle Satellite Cultured Cells --
17 chr3:99115200-99116000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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