Variant report
| Variant | rs9483483 |
|---|---|
| Chromosome Location | chr6:132929083-132929084 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:132920200-132929800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 2 | chr6:132926200-132933600 | Weak transcription | Stomach Mucosa | stomach |
| 3 | chr6:132926600-132931800 | Weak transcription | Small Intestine | intestine |
| 4 | chr6:132928000-132935200 | Enhancers | Fetal Intestine Small | intestine |
| 5 | chr6:132928200-132932200 | Enhancers | Fetal Intestine Large | intestine |
| 6 | chr6:132928600-132930000 | Enhancers | Liver | Liver |
| 7 | chr6:132928800-132929400 | Enhancers | Duodenum Mucosa | Duodenum |
| 8 | chr6:132928800-132929600 | Weak transcription | Pancreas | Pancrea |
| 9 | chr6:132929000-132933600 | Weak transcription | HepG2 | liver |
