Variant report
| Variant | rs4298992 |
|---|---|
| Chromosome Location | chr12:25504836-25504837 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:25501000-25505000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 2 | chr12:25501200-25505000 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 3 | chr12:25501400-25510800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 4 | chr12:25502200-25506400 | Weak transcription | Thymus | Thymus |
| 5 | chr12:25504600-25505400 | Enhancers | GM12878-XiMat | blood |
| 6 | chr12:25504800-25505400 | Enhancers | Primary T helper cells fromperipheralblood | blood |
| 7 | chr12:25504800-25505400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
