| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33289186-33289661 | Common:4; Rare:106 | ||||
| chr6:33298905-33299064 | Rare:42 | ||||
| chr6:33299397-33299540 | Common:1; Rare:33 | ||||
| chr6:33314056-33314135 | Common:2; Rare:23 | ||||
| chr6:33322898-33323318 | Common:5; Rare:129 | ||||
| chr6:33391303-33391493 | Common:1; Rare:31 | ||||
| chr6:33410901-33411072 | Rare:34 | ||||
| chr6:33417864-33417998 | Rare:58 | ||||
| chr6:33418000-33418474 | Common:3; Rare:115 | ||||
| chr6:33454383-33454607 | Rare:66 | ||||
| chr6:33620190-33620261 | Rare:11 | ||||
| chr6:34236752-34236927 | Common:2; Rare:71 | ||||
| chr6:34392268-34392456 | Rare:78 | ||||
| chr6:34392458-34392654 | Rare:69 | ||||
| chr6:34425942-34426185 | Common:5; Rare:97; Clinvar:1; Clinvar (benign):8 |