Variant report

Variant rs7795498
Chromosome Location chr7:78811764-78811765
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:78805600-78814800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr7:78811200-78812400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr7:78811200-78812400 Enhancers Muscle Satellite Cultured Cells --
4 chr7:78811400-78812000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr7:78811400-78812000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr7:78811400-78812200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:78811400-78812400 Enhancers NH-A brain
8 chr7:78811600-78812000 Enhancers NHEK skin
9 chr7:78811600-78812200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr7:78811600-78812200 Enhancers HMEC breast
11 chr7:78811600-78812400 Enhancers Osteobl bone

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