Variant report

Variant rs189057596
Chromosome Location chr20:29525621-29525622
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:29521000-29534000 Weak transcription Gastric stomach
2 chr20:29524000-29525800 Active TSS Primary T regulatory cells fromperipheralblood blood
3 chr20:29524800-29535000 Weak transcription Pancreas Pancrea
4 chr20:29525000-29528400 Weak transcription Brain Substantia Nigra brain
5 chr20:29525000-29535200 Weak transcription Small Intestine intestine
6 chr20:29525200-29525800 Enhancers Primary hematopoietic stem cells blood
7 chr20:29525200-29525800 Enhancers Primary T helper naive cells from peripheral blood blood
8 chr20:29525200-29525800 Enhancers Primary Natural Killer cells fromperipheralblood blood
9 chr20:29525400-29525800 Flanking Active TSS Dnd41 blood
10 chr20:29525400-29525800 Enhancers HepG2 liver
11 chr20:29525600-29525800 Enhancers Primary T killer memory cells from peripheral blood blood
12 chr20:29525600-29525800 Flanking Active TSS K562 blood
13 chr20:29525600-29529600 Weak transcription Duodenum Mucosa Duodenum
14 chr20:29525600-29531000 Weak transcription Stomach Mucosa stomach
15 chr20:29525600-29535200 Weak transcription Right Atrium heart

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