Variant report

Variant rs10758653
Chromosome Location chr9:489338-489339
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:486200-495200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr9:487600-489800 Enhancers Stomach Mucosa stomach
3 chr9:488200-489600 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr9:488400-490200 Weak transcription Pancreas Pancrea
5 chr9:488400-490400 Enhancers Liver Liver
6 chr9:488400-490400 Enhancers HepG2 liver
7 chr9:488400-495400 Weak transcription Right Atrium heart
8 chr9:488600-490000 Enhancers Fetal Lung lung
9 chr9:488600-490600 Enhancers Rectal Mucosa Donor 31 rectum
10 chr9:488800-495800 Weak transcription Gastric stomach
11 chr9:489000-489400 Enhancers A549 lung
12 chr9:489000-489600 Enhancers Rectal Mucosa Donor 29 rectum
13 chr9:489200-489600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr9:489200-490600 Enhancers Sigmoid Colon Sigmoid Colon

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