Variant report

Variant rs1507516
Chromosome Location chr2:234960570-234960571
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234959400-234961000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:234959400-234961000 Enhancers NHDF-Ad bronchial
3 chr2:234959400-234961400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:234959600-234960600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr2:234959600-234961200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:234959800-234960600 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr2:234959800-234961400 Enhancers NHEK skin
8 chr2:234960000-234960600 Enhancers HMEC breast
9 chr2:234960000-234960600 Enhancers NH-A brain
10 chr2:234960000-234961400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:234960200-234961600 Flanking Active TSS Liver Liver

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