| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30534525-30534647 | Common:1; Rare:45 | ||||
| chr16:30534847-30535089 | Common:3; Rare:81 | ||||
| chr16:30558268-30558487 | Common:3; Rare:50 | ||||
| chr16:30571562-30571718 | Rare:47 | ||||
| chr16:30585502-30585902 | Common:1; Rare:94 | ||||
| chr16:30650735-30651002 | Rare:79 | ||||
| chr16:30651407-30651606 | Rare:44 | ||||
| chr16:30658652-30658859 | Common:1; Rare:62 | ||||
| chr16:30659843-30659929 | Rare:45 | ||||
| chr16:30698181-30698357 | Rare:82 | ||||
| chr16:30698447-30698735 | Common:1; Rare:104 | ||||
| chr16:30698979-30699192 | Rare:79; Clinvar (benign):1 | ||||
| chr16:30748125-30748468 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761454-30761597 | Rare:58 | ||||
| chr16:30762058-30762343 | Common:3; Rare:93 |