Variant report
Variant | rs10759269 |
---|---|
Chromosome Location | chr9:110701704-110701705 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:110695800-110705200 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
2 | chr9:110696200-110707800 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr9:110700400-110702200 | Enhancers | Primary hematopoietic stem cells | blood |
4 | chr9:110701000-110702000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
5 | chr9:110701000-110702200 | Enhancers | Fetal Intestine Large | intestine |
6 | chr9:110701000-110702200 | Enhancers | Fetal Intestine Small | intestine |
7 | chr9:110701200-110703800 | Enhancers | Placenta Amnion | Placenta Amnion |
8 | chr9:110701400-110702400 | Weak transcription | Spleen | Spleen |
9 | chr9:110701600-110702200 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
10 | chr9:110701600-110705000 | Weak transcription | Primary monocytes fromperipheralblood | blood |