Variant report
| Variant | rs2212598 |
|---|---|
| Chromosome Location | chr21:39897884-39897885 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr21:39896000-39910400 | Weak transcription | Small Intestine | intestine |
| 2 | chr21:39896400-39899400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 3 | chr21:39896600-39900200 | Enhancers | HepG2 | liver |
| 4 | chr21:39897800-39899000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 5 | chr21:39897800-39903000 | Weak transcription | Aorta | Aorta |
