Variant report

Variant rs492934
Chromosome Location chr9:257985-257986
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:219000-261400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr9:255000-259400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr9:255000-268600 Weak transcription Spleen Spleen
4 chr9:255000-270400 Weak transcription Pancreas Pancrea
5 chr9:255000-271800 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr9:255600-260000 Enhancers Primary monocytes fromperipheralblood blood
7 chr9:257000-265800 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr9:257200-258600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
9 chr9:257400-259200 Enhancers Primary B cells from cord blood blood
10 chr9:257600-258600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
11 chr9:257800-258400 Enhancers Primary B cells from peripheral blood blood
12 chr9:257800-258600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr9:257800-258800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr9:257800-259800 Enhancers K562 blood
15 chr9:257800-260200 Enhancers Primary hematopoietic stem cells blood
16 chr9:257800-260200 Enhancers Primary hematopoietic stem cells short term culture blood

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