| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32838219-32838348 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr6:32838705-32838979 | Common:6; Rare:44 | ||||
| chr6:32844001-32844097 | Rare:24; Clinvar:1 | ||||
| chr6:32844631-32844822 | Common:1; Rare:41 | ||||
| chr6:32853979-32854216 | Common:2; Rare:56 | ||||
| chr6:32969788-32970050 | Rare:69 | ||||
| chr6:32970736-32970946 | Common:1; Rare:60 | ||||
| chr6:33200656-33200972 | Common:3; Rare:93 | ||||
| chr6:33208438-33208522 | Rare:22 | ||||
| chr6:33271650-33272122 | Common:2; Rare:168 | ||||
| chr6:33289149-33289644 | Common:4; Rare:118 | ||||
| chr6:33298924-33299058 | Rare:33 | ||||
| chr6:33299417-33299486 | Common:1; Rare:14 | ||||
| chr6:33418004-33418508 | Common:3; Rare:120 | ||||
| chr6:33420028-33420271 | Rare:53 |