Variant report
| Variant | rs4952038 |
|---|---|
| Chromosome Location | chr2:31272992-31272993 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:31267400-31273200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 2 | chr2:31272200-31274000 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 3 | chr2:31272200-31275600 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
| 4 | chr2:31272400-31273600 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr2:31272800-31273200 | Weak transcription | Fetal Intestine Small | intestine |
| 6 | chr2:31272800-31273200 | Weak transcription | Fetal Kidney | kidney |
| 7 | chr2:31272800-31274400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
