Variant report

Variant rs28903693
Chromosome Location chr2:234953141-234953142
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:234952200-234953600 Enhancers A549 lung
2 chr2:234952400-234953400 Enhancers HUVEC blood vessel
3 chr2:234952400-234953400 Enhancers NHEK skin
4 chr2:234952600-234953400 Enhancers Muscle Satellite Cultured Cells --
5 chr2:234952600-234953400 Enhancers NHDF-Ad bronchial
6 chr2:234952600-234953600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr2:234952600-234953600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr2:234952800-234953200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:234953000-234956000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:234953000-234956600 Weak transcription HMEC breast

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