| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107886756-107886881 | Common:2; Rare:38 | ||||
| chr6:107924577-107924827 | Common:1; Rare:51 | ||||
| chr6:108004417-108004647 | Common:3; Rare:33 | ||||
| chr6:108033112-108033217 | Common:1; Rare:20 | ||||
| chr6:108215787-108215835 | Rare:5 | ||||
| chr6:108945393-108945587 | Rare:31 | ||||
| chr6:108986361-108986449 | Common:1; Rare:24 | ||||
| chr6:109175504-109175685 | Rare:34 | ||||
| chr6:109376074-109376154 | Rare:25 | ||||
| chr6:109476140-109476205 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr6:110960371-110960474 | Common:2; Rare:37 | ||||
| chr6:111336245-111336253 | Rare:2 | ||||
| chr6:111338361-111338403 | Rare:4 | ||||
| chr6:111563003-111563209 | Rare:32 | ||||
| chr6:111779465-111779514 | Rare:4 |