Variant report
| Variant | rs13204927 |
|---|---|
| Chromosome Location | chr6:109602790-109602791 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:109587600-109614600 | Weak transcription | HepG2 | liver |
| 2 | chr6:109591600-109615200 | Weak transcription | Placenta | Placenta |
| 3 | chr6:109602600-109603000 | Enhancers | Primary monocytes fromperipheralblood | blood |
