| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:95577407-95577553 | Common:3; Rare:40 | ||||
| chr6:96521671-96521866 | Common:8; Rare:94 | ||||
| chr6:97283170-97283360 | Common:2; Rare:59 | ||||
| chr6:99424874-99424929 | Rare:21 | ||||
| chr6:99425251-99425506 | Common:2; Rare:70 | ||||
| chr6:100881261-100881498 | Common:5; Rare:96 | ||||
| chr6:106325594-106325906 | Common:1; Rare:112 | ||||
| chr6:106629466-106629645 | Common:3; Rare:41 | ||||
| chr6:107459535-107459641 | Common:1; Rare:29 | ||||
| chr6:108260914-108261112 | Rare:93 | ||||
| chr6:108560730-108560924 | Rare:86 | ||||
| chr6:109009476-109009682 | Common:2; Rare:65 | ||||
| chr6:109382270-109382311 | Rare:17 | ||||
| chr6:109382377-109382838 | Common:6; Rare:151; Clinvar (benign):1 | ||||
| chr6:109440532-109440887 | Common:2; Rare:128 |