Variant report
| Variant | rs17728162 |
|---|---|
| Chromosome Location | chr18:28847656-28847657 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr18:28842400-28849000 | Weak transcription | HepG2 | liver |
| 2 | chr18:28842600-28849200 | Weak transcription | Fetal Kidney | kidney |
| 3 | chr18:28844000-28847800 | Weak transcription | Stomach Mucosa | stomach |
| 4 | chr18:28844600-28847800 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr18:28845800-28848800 | Weak transcription | Liver | Liver |
| 6 | chr18:28847200-28848000 | Weak transcription | NHEK | skin |
| 7 | chr18:28847400-28847800 | Enhancers | GM12878-XiMat | blood |
| 8 | chr18:28847600-28850400 | Enhancers | Fetal Intestine Small | intestine |
