Variant report
| Variant | rs17020918 |
|---|---|
| Chromosome Location | chr1:213706839-213706840 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:213704000-213707000 | Enhancers | Brain Germinal Matrix | brain |
| 2 | chr1:213704200-213707400 | Weak transcription | Right Atrium | heart |
| 3 | chr1:213705600-213709000 | Weak transcription | Pancreas | Pancrea |
| 4 | chr1:213706200-213707400 | Enhancers | Fetal Intestine Small | intestine |
| 5 | chr1:213706200-213707400 | Enhancers | HepG2 | liver |
| 6 | chr1:213706400-213707200 | Enhancers | Fetal Intestine Large | intestine |
| 7 | chr1:213706800-213707400 | Enhancers | Fetal Heart | heart |
