Variant report

Variant rs16927796
Chromosome Location chr10:27673128-27673129
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:27672200-27673600 Enhancers Hela-S3 cervix
2 chr10:27672600-27673200 Enhancers HepG2 liver
3 chr10:27672600-27673200 Enhancers Monocytes-CD14+_RO01746 blood
4 chr10:27672600-27673400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr10:27672600-27673400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr10:27672600-27673400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr10:27672600-27673400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr10:27672600-27673400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr10:27672600-27673400 Enhancers Pancreatic Islets Pancreatic Islet
10 chr10:27672600-27673400 Enhancers Lung lung
11 chr10:27672600-27673400 Flanking Active TSS A549 lung
12 chr10:27672600-27673400 Enhancers HMEC breast
13 chr10:27672600-27673400 Enhancers NHEK skin
14 chr10:27672800-27673400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr10:27672800-27673400 Enhancers Stomach Mucosa stomach
16 chr10:27672800-27673400 Enhancers HUVEC blood vessel
17 chr10:27673000-27673400 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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