| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19718521-19718574 | Rare:19 | ||||
| chr16:20806433-20806661 | Rare:73 | ||||
| chr16:22206213-22206326 | Rare:42 | ||||
| chr16:22437360-22437667 | Common:2; Rare:89 | ||||
| chr16:23452688-23452794 | Rare:36 | ||||
| chr16:23453159-23453236 | Rare:20 | ||||
| chr16:23557327-23557550 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641228-23641551 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678634-23678947 | Common:5; Rare:96 | ||||
| chr16:24539375-24539591 | Rare:77 | ||||
| chr16:24729611-24729738 | Common:6; Rare:69 | ||||
| chr16:25015265-25015457 | Common:2; Rare:67 | ||||
| chr16:25111544-25111797 | Common:2; Rare:66 | ||||
| chr16:27268719-27268872 | Common:1; Rare:52 | ||||
| chr16:27549886-27550167 | Common:2; Rare:104 |