Variant report
| Variant | rs1245436 |
|---|---|
| Chromosome Location | chr12:62525170-62525171 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:62519800-62525600 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 2 | chr12:62522600-62526600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 3 | chr12:62524000-62526000 | Flanking Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 4 | chr12:62524000-62526200 | Enhancers | Primary hematopoietic stem cells | blood |
| 5 | chr12:62524600-62525200 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 6 | chr12:62524600-62525400 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 7 | chr12:62524600-62525400 | Flanking Active TSS | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 8 | chr12:62524800-62525400 | Enhancers | H1 Cell Line | embryonic stem cell |
