Variant report

Variant rs10173947
Chromosome Location chr2:151150611-151150612
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:151143200-151151600 Weak transcription Aorta Aorta
2 chr2:151143800-151153000 Weak transcription NHDF-Ad bronchial
3 chr2:151149400-151151200 Enhancers HMEC breast
4 chr2:151149600-151151000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:151150000-151150800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:151150000-151151200 Enhancers NHEK skin
7 chr2:151150000-151152200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr2:151150200-151150800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:151150400-151150800 Enhancers Breast Myoepithelial Primary Cells Breast

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