| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33201820-33202120 | Common:4; Rare:77 | ||||
| chr6:33208443-33208524 | Rare:22 | ||||
| chr6:33271632-33272122 | Common:3; Rare:177 | ||||
| chr6:33289268-33289644 | Common:3; Rare:75 | ||||
| chr6:33298924-33299020 | Rare:26 | ||||
| chr6:33299408-33299495 | Common:1; Rare:15 | ||||
| chr6:33314213-33314467 | Common:3; Rare:41 | ||||
| chr6:33322934-33323261 | Common:5; Rare:96 | ||||
| chr6:33418039-33418488 | Common:3; Rare:109 | ||||
| chr6:33420071-33420301 | Rare:47; Clinvar (benign):1 | ||||
| chr6:33454398-33454601 | Rare:58 | ||||
| chr6:33711631-33711811 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr6:34248472-34248555 | Rare:11 | ||||
| chr6:34248977-34249322 | Common:1; Rare:89 | ||||
| chr6:34392154-34392643 | Common:1; Rare:194 |