| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:291974-292320 | Common:1; Rare:62 | ||||
| chr6:693069-693372 | Common:1; Rare:79 | ||||
| chr6:1311807-1312271 | Common:3; Rare:142 | ||||
| chr6:1312275-1312360 | Rare:24 | ||||
| chr6:1312513-1312679 | Common:1; Rare:44 | ||||
| chr6:1312854-1313054 | Common:3; Rare:65 | ||||
| chr6:2245453-2245833 | Common:1; Rare:131 | ||||
| chr6:2841850-2842295 | Common:5; Rare:77 | ||||
| chr6:2999644-2999999 | Common:10; Rare:74 | ||||
| chr6:3068469-3068577 | Common:1; Rare:32 | ||||
| chr6:3118587-3118775 | Common:3; Rare:66 | ||||
| chr6:3157413-3157676 | Common:6; Rare:85; Clinvar (benign):1 | ||||
| chr6:3455986-3455995 | Rare:2 | ||||
| chr6:3456170-3456212 | Rare:7 | ||||
| chr6:3751339-3751389 | Rare:13 |