Variant report

Variant rs41313299
Chromosome Location chr9:116824945-116824946
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116812200-116827400 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr9:116816000-116825600 Weak transcription Fetal Brain Female brain
3 chr9:116822000-116832400 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr9:116822600-116833400 Genic enhancers HepG2 liver
5 chr9:116824200-116825000 Enhancers Gastric stomach
6 chr9:116824200-116825600 Enhancers Fetal Intestine Small intestine
7 chr9:116824200-116825800 Enhancers Fetal Intestine Large intestine
8 chr9:116824400-116825200 Enhancers Stomach Mucosa stomach
9 chr9:116824600-116825000 Enhancers Duodenum Mucosa Duodenum
10 chr9:116824600-116830600 Genic enhancers Liver Liver
11 chr9:116824800-116825000 Enhancers Right Ventricle heart
12 chr9:116824800-116828200 Weak transcription Pancreas Pancrea

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