Variant report
| Variant | rs376826904 |
|---|---|
| Chromosome Location | chr1:172485757-172485758 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:172480800-172487800 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 2 | chr1:172484400-172487600 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 3 | chr1:172484600-172487600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 4 | chr1:172484600-172487800 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 5 | chr1:172484800-172487800 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 6 | chr1:172485200-172486800 | Weak transcription | K562 | blood |
| 7 | chr1:172485200-172488400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 8 | chr1:172485400-172486200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
| 9 | chr1:172485400-172486600 | Weak transcription | Primary hematopoietic stem cells | blood |
