| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32853686-32853777 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32854023-32854228 | Common:2; Rare:53 | ||||
| chr6:32968454-32968616 | Common:3; Rare:43 | ||||
| chr6:32970738-32970946 | Common:1; Rare:59 | ||||
| chr6:33200356-33200432 | Rare:18 | ||||
| chr6:33200654-33200938 | Common:2; Rare:85 | ||||
| chr6:33208277-33208533 | Common:2; Rare:55 | ||||
| chr6:33271646-33272302 | Common:4; Rare:214 | ||||
| chr6:33288985-33289093 | Rare:40 | ||||
| chr6:33289174-33289848 | Common:4; Rare:165 | ||||
| chr6:33298914-33299070 | Rare:40 | ||||
| chr6:33299417-33299510 | Common:1; Rare:22 | ||||
| chr6:33314197-33314565 | Common:6; Rare:57 | ||||
| chr6:33323012-33323307 | Common:4; Rare:84 | ||||
| chr6:33391556-33391923 | Common:3; Rare:83 |