| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15563444-15563755 | Common:1; Rare:100 | ||||
| chr17:15699497-15699773 | Common:3; Rare:72 | ||||
| chr17:15999579-16000003 | Common:3; Rare:185; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16215454-16215657 | Common:2; Rare:90 | ||||
| chr17:16217073-16217240 | Rare:44; Clinvar:1 | ||||
| chr17:16380681-16380814 | Common:2; Rare:29 | ||||
| chr17:16419245-16419355 | Rare:30 | ||||
| chr17:17237432-17237698 | Common:4; Rare:60 | ||||
| chr17:17281182-17281400 | Rare:85 | ||||
| chr17:17476871-17477196 | Common:3; Rare:103 | ||||
| chr17:17496383-17496559 | Rare:45 | ||||
| chr17:17591582-17591936 | Common:2; Rare:101 | ||||
| chr17:17816245-17816521 | Rare:90 | ||||
| chr17:17823586-17823959 | Common:5; Rare:143 | ||||
| chr17:17836783-17837084 | Common:3; Rare:71 |