| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33208380-33208524 | Common:1; Rare:33 | ||||
| chr6:33271655-33272122 | Common:2; Rare:166 | ||||
| chr6:33289174-33289383 | Common:1; Rare:58 | ||||
| chr6:33298924-33299064 | Rare:36 | ||||
| chr6:33313858-33313999 | Common:1; Rare:50 | ||||
| chr6:33320383-33320804 | Common:2; Rare:125; Clinvar (pathogenic):1 | ||||
| chr6:33323012-33323310 | Common:4; Rare:86 | ||||
| chr6:33417142-33417510 | Common:1; Rare:106 | ||||
| chr6:33417864-33417952 | Rare:38 | ||||
| chr6:33418030-33418306 | Common:2; Rare:75 | ||||
| chr6:33454415-33454601 | Rare:48 | ||||
| chr6:33580185-33580404 | Common:3; Rare:59 | ||||
| chr6:34236752-34236935 | Common:2; Rare:73 | ||||
| chr6:34248977-34249218 | Rare:54 | ||||
| chr6:34392339-34392648 | Rare:122 |