Variant report
| Variant | rs16996607 |
|---|---|
| Chromosome Location | chr21:40001192-40001193 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr21:39995200-40002400 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 2 | chr21:39996600-40001800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 3 | chr21:40000600-40001400 | Enhancers | Aorta | Aorta |
| 4 | chr21:40000800-40002400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
| 5 | chr21:40001000-40002600 | Genic enhancers | Breast Myoepithelial Primary Cells | Breast |
