| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7394455-7394997 | Common:3; Rare:134 | ||||
| chr17:7395018-7395073 | Rare:5 | ||||
| chr17:7403555-7403903 | Common:7; Rare:93 | ||||
| chr17:7403988-7404368 | Common:1; Rare:120 | ||||
| chr17:7404433-7404968 | Common:6; Rare:132 | ||||
| chr17:7405197-7405284 | Rare:17 | ||||
| chr17:7435265-7435514 | Common:1; Rare:52 | ||||
| chr17:7435520-7435659 | Common:2; Rare:27 | ||||
| chr17:7435837-7436230 | Common:3; Rare:145 | ||||
| chr17:7445393-7445443 | Rare:17 | ||||
| chr17:7455288-7455594 | Common:4; Rare:95; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:7455607-7455671 | Common:1; Rare:9 | ||||
| chr17:7455772-7456043 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7479430-7479818 | Common:5; Rare:66 | ||||
| chr17:7479823-7479966 | Common:1; Rare:32 |