Variant report

Variant rs2977002
Chromosome Location chr8:52285963-52285964
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:52283000-52289800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:52283800-52287400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr8:52284600-52294400 Weak transcription Right Ventricle heart
4 chr8:52284600-52296000 Weak transcription Left Ventricle heart
5 chr8:52285800-52286000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:52285800-52286000 Enhancers NHDF-Ad bronchial
7 chr8:52285800-52286600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr8:52285800-52286800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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