Variant report

Variant rs546900805
Chromosome Location chr8:53408941-53408942
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:53408400-53409000 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
2 chr8:53408400-53409000 Active TSS Brain Hippocampus Middle brain
3 chr8:53408400-53409000 Active TSS Brain Inferior Temporal Lobe brain
4 chr8:53408400-53409000 Active TSS Pancreatic Islets Pancreatic Islet
5 chr8:53408400-53409200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr8:53408400-53409200 Enhancers Hela-S3 cervix
7 chr8:53408600-53409000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr8:53408600-53409000 Bivalent/Poised TSS Duodenum Mucosa Duodenum
9 chr8:53408600-53409000 Bivalent/Poised TSS Rectal Mucosa Donor 31 rectum
10 chr8:53408600-53409000 Enhancers NHEK skin
11 chr8:53408600-53409200 Enhancers HUES64 Cell Line embryonic stem cell
12 chr8:53408800-53409000 Bivalent/Poised TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr8:53408800-53409000 Active TSS Brain Anterior Caudate brain
14 chr8:53408800-53409200 Enhancers Brain Substantia Nigra brain
15 chr8:53408800-53409200 Bivalent Enhancer HepG2 liver

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