| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33418071-33418455 | Common:2; Rare:89 | ||||
| chr6:33420027-33420267 | Rare:51 | ||||
| chr6:33454406-33454604 | Rare:56 | ||||
| chr6:34236755-34236906 | Common:2; Rare:62 | ||||
| chr6:34392337-34392408 | Rare:36 | ||||
| chr6:34424761-34425194 | Common:3; Rare:113; Clinvar (benign):5 | ||||
| chr6:34426019-34426195 | Common:5; Rare:74; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696738-34696988 | Common:1; Rare:60 | ||||
| chr6:34757385-34757550 | Rare:52 | ||||
| chr6:35259439-35259533 | Rare:25 | ||||
| chr6:35688900-35689116 | Common:1; Rare:73 | ||||
| chr6:35921047-35921261 | Common:1; Rare:90 | ||||
| chr6:36442904-36443077 | Common:2; Rare:70 | ||||
| chr6:36547429-36547569 | Rare:63 | ||||
| chr6:36594232-36594432 | Common:3; Rare:86 |