| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30571203-30571559 | Common:1; Rare:115 | ||||
| chr6:30616982-30617041 | Rare:25 | ||||
| chr6:30617754-30617878 | Rare:51 | ||||
| chr6:30647303-30647471 | Common:3; Rare:63 | ||||
| chr6:30686631-30686757 | Common:1; Rare:25 | ||||
| chr6:30717243-30717435 | Common:1; Rare:39 | ||||
| chr6:30720124-30720429 | Common:1; Rare:79 | ||||
| chr6:30742480-30742985 | Common:3; Rare:117 | ||||
| chr6:30744288-30744371 | Rare:20 | ||||
| chr6:30880650-30880786 | Rare:25 | ||||
| chr6:30907901-30908240 | Common:3; Rare:81 | ||||
| chr6:30914007-30914377 | Common:2; Rare:114; Clinvar (benign):2 | ||||
| chr6:31158165-31158552 | Common:8; Rare:92 | ||||
| chr6:31272064-31272260 | Common:13; Rare:29 | ||||
| chr6:31399742-31399786 | Rare:11 |