Variant report

Variant rs10425667
Chromosome Location chr19:52287051-52287052
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52280800-52294000 Enhancers Primary monocytes fromperipheralblood blood
2 chr19:52281600-52287800 Weak transcription Placenta Placenta
3 chr19:52281800-52287800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr19:52286600-52289000 Enhancers K562 blood
5 chr19:52286800-52287200 Enhancers Primary B cells from peripheral blood blood
6 chr19:52286800-52287200 Enhancers Placenta Amnion Placenta Amnion
7 chr19:52286800-52287400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr19:52286800-52289000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr19:52286800-52289200 Enhancers NHEK skin
10 chr19:52287000-52287400 Enhancers HMEC breast
11 chr19:52287000-52287800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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