| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30557208-30557369 | Common:1; Rare:58 | ||||
| chr6:30571191-30571526 | Common:1; Rare:107 | ||||
| chr6:30606803-30606902 | Rare:20 | ||||
| chr6:30617783-30617878 | Rare:38 | ||||
| chr6:30647263-30647465 | Common:2; Rare:79 | ||||
| chr6:30686643-30686763 | Common:1; Rare:22 | ||||
| chr6:30717261-30717435 | Common:1; Rare:36 | ||||
| chr6:30717442-30717653 | Common:2; Rare:47 | ||||
| chr6:30720124-30720436 | Common:1; Rare:80 | ||||
| chr6:30742474-30742968 | Common:3; Rare:114 | ||||
| chr6:30882854-30882992 | Common:1; Rare:17 | ||||
| chr6:30914190-30914387 | Rare:72; Clinvar (benign):2 | ||||
| chr6:31158160-31158641 | Common:9; Rare:116 | ||||
| chr6:31399741-31400033 | Common:5; Rare:49 | ||||
| chr6:31541938-31542316 | Common:7; Rare:99 |