| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3500831-3501053 | Common:3; Rare:81 | ||||
| chr16:3611558-3611795 | Rare:102; Clinvar:1 | ||||
| chr16:3717509-3717618 | Rare:57 | ||||
| chr16:4425778-4425884 | Common:1; Rare:49 | ||||
| chr16:4476306-4476459 | Common:1; Rare:57 | ||||
| chr16:4538394-4538531 | Common:2; Rare:39 | ||||
| chr16:4538747-4538899 | Rare:62 | ||||
| chr16:4693453-4693729 | Common:2; Rare:117 | ||||
| chr16:4734199-4734282 | Common:1; Rare:29 | ||||
| chr16:4767114-4767308 | Common:2; Rare:68 | ||||
| chr16:4802878-4803050 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:4847261-4847478 | Common:2; Rare:95 | ||||
| chr16:5097740-5098016 | Common:4; Rare:96 | ||||
| chr16:6019419-6019747 | Common:1; Rare:119 | ||||
| chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 |