Variant report

Variant rs116648833
Chromosome Location chr14:21423082-21423083
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:21420000-21423200 Enhancers Primary neutrophils fromperipheralblood blood
2 chr14:21420200-21423200 Enhancers Primary monocytes fromperipheralblood blood
3 chr14:21420200-21423600 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr14:21421800-21423200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr14:21422400-21424000 Enhancers Liver Liver
6 chr14:21422400-21425400 Enhancers Fetal Thymus thymus
7 chr14:21422600-21424400 Enhancers HepG2 liver
8 chr14:21423000-21423600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr14:21423000-21424600 Active TSS Brain Hippocampus Middle brain
10 chr14:21423000-21424600 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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