Variant report

Variant rs66587337
Chromosome Location chr9:21799383-21799384
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21790200-21801000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:21790200-21801200 Weak transcription NHEK skin
3 chr9:21796800-21800000 Weak transcription Placenta Placenta
4 chr9:21796800-21801200 Weak transcription NHDF-Ad bronchial
5 chr9:21797200-21801000 Weak transcription Osteobl bone
6 chr9:21797400-21801200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr9:21797400-21801200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr9:21797800-21801400 Weak transcription A549 lung
9 chr9:21798000-21801600 Weak transcription Aorta Aorta

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