Variant report
| Variant | rs7669929 |
|---|---|
| Chromosome Location | chr4:142060330-142060331 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr4:142056000-142062000 | Weak transcription | Rectal Smooth Muscle | rectum |
| 2 | chr4:142056400-142061800 | Weak transcription | Primary hematopoietic stem cells | blood |
| 3 | chr4:142056600-142061200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
| 4 | chr4:142056600-142061800 | Weak transcription | Fetal Stomach | stomach |
| 5 | chr4:142056600-142063600 | Weak transcription | Left Ventricle | heart |
| 6 | chr4:142056800-142061200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
| 7 | chr4:142056800-142062000 | Weak transcription | Fetal Heart | heart |
| 8 | chr4:142057200-142061400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 9 | chr4:142060000-142063000 | Enhancers | Fetal Muscle Leg | muscle |
| 10 | chr4:142060200-142060400 | Flanking Active TSS | H1 Derived Mesenchymal Stem Cells | ES cell derived |
