Variant report

Variant rs117598789
Chromosome Location chr20:15119884-15119885
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:15119000-15120200 Enhancers Liver Liver
2 chr20:15119200-15120000 Enhancers A549 lung
3 chr20:15119200-15120000 Enhancers HepG2 liver
4 chr20:15119200-15120200 Enhancers Stomach Mucosa stomach
5 chr20:15119200-15120600 Enhancers Fetal Intestine Large intestine
6 chr20:15119600-15120000 Flanking Active TSS Pancreatic Islets Pancreatic Islet
7 chr20:15119600-15120200 Enhancers Fetal Intestine Small intestine
8 chr20:15119600-15125200 Weak transcription Fetal Heart heart
9 chr20:15119800-15120200 Enhancers Brain Germinal Matrix brain
10 chr20:15119800-15127400 Weak transcription Fetal Kidney kidney

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