Variant report

Variant rs6950869
Chromosome Location chr7:17652915-17652916
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17641600-17663000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:17642400-17657400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr7:17648600-17653000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:17648800-17663200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr7:17652000-17653000 Weak transcription Liver Liver
6 chr7:17652800-17653200 Enhancers HMEC breast
7 chr7:17652800-17653400 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived

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