| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16215407-16216010 | Common:8; Rare:226 | ||||
| chr17:16216044-16216187 | Rare:46 | ||||
| chr17:16217008-16217295 | Rare:82; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:16353115-16353250 | Rare:52 | ||||
| chr17:16353411-16353535 | Rare:42 | ||||
| chr17:16381024-16381423 | Common:4; Rare:174 | ||||
| chr17:16415043-16415352 | Common:2; Rare:58 | ||||
| chr17:16415447-16415811 | Common:4; Rare:84 | ||||
| chr17:16419238-16419360 | Rare:34 | ||||
| chr17:16419623-16419800 | Common:1; Rare:37 | ||||
| chr17:16569140-16569399 | Common:1; Rare:75 | ||||
| chr17:16653536-16653872 | Common:2; Rare:106 | ||||
| chr17:16971860-16972334 | Common:1; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:17042124-17042494 | Common:19; Rare:129 | ||||
| chr17:17206227-17206614 | Common:4; Rare:149 |