Variant report

Variant rs58500868
Chromosome Location chr19:52286813-52286814
allele A/G
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 chr19:52281800-52287000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr19:52281800-52287800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr19:52283800-52287000 Enhancers Primary neutrophils fromperipheralblood blood
6 chr19:52286600-52289000 Enhancers K562 blood
7 chr19:52286800-52287200 Enhancers Primary B cells from peripheral blood blood
8 chr19:52286800-52287200 Enhancers Placenta Amnion Placenta Amnion
9 chr19:52286800-52287400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
10 chr19:52286800-52289000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr19:52286800-52289200 Enhancers NHEK skin

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