Variant report

Variant rs73369008
Chromosome Location chr9:494631-494632
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr9:488400-495400 Weak transcription Right Atrium heart
3 chr9:488800-495800 Weak transcription Gastric stomach
4 chr9:489600-495200 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr9:489600-503200 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr9:493400-495400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr9:494400-495400 Enhancers Rectal Mucosa Donor 31 rectum
8 chr9:494400-496200 Enhancers A549 lung
9 chr9:494400-496200 Enhancers HepG2 liver
10 chr9:494400-496400 Enhancers Stomach Mucosa stomach
11 chr9:494600-494800 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
12 chr9:494600-495400 Bivalent Enhancer Liver Liver
13 chr9:494600-495400 Enhancers Pancreatic Islets Pancreatic Islet
14 chr9:494600-495400 Weak transcription Sigmoid Colon Sigmoid Colon
15 chr9:494600-496200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
16 chr9:494600-496400 Enhancers Pancreas Pancrea

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