Variant report
| Variant | rs17682059 |
|---|---|
| Chromosome Location | chr10:18557547-18557548 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:18550600-18561600 | Weak transcription | Ovary | ovary |
| 2 | chr10:18551000-18559600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
| 3 | chr10:18554000-18566400 | Weak transcription | Aorta | Aorta |
| 4 | chr10:18554000-18571000 | Weak transcription | Fetal Heart | heart |
| 5 | chr10:18555200-18558000 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 6 | chr10:18556600-18557600 | Bivalent Enhancer | Foreskin Melanocyte Primary Cells skin03 | Skin |
