Variant report
| Variant | rs28494703 |
|---|---|
| Chromosome Location | chr4:81508800-81508801 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:81502200-81509000 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
| 2 | chr4:81508000-81509000 | Enhancers | Fetal Kidney | kidney |
| 3 | chr4:81508400-81509600 | Bivalent Enhancer | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 4 | chr4:81508600-81509400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 5 | chr4:81508800-81509000 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
| 6 | chr4:81508800-81509000 | Enhancers | HMEC | breast |
| 7 | chr4:81508800-81509200 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 8 | chr4:81508800-81509200 | Enhancers | Primary hematopoietic stem cells | blood |
