Variant report
| Variant | rs1411667 |
|---|---|
| Chromosome Location | chr9:85107628-85107629 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:85103800-85109400 | Weak transcription | NHLF | lung |
| 2 | chr9:85104600-85107800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 3 | chr9:85105200-85111200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
| 4 | chr9:85105600-85111000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 5 | chr9:85105800-85111200 | Weak transcription | Adipose Nuclei | Adipose |
| 6 | chr9:85105800-85113400 | Weak transcription | Fetal Lung | lung |
| 7 | chr9:85107600-85111000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
