| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8487432-8487742 | Rare:89; Clinvar (benign):1 | ||||
| chr17:8490538-8490709 | Common:2; Rare:37 | ||||
| chr17:8492354-8492706 | Common:5; Rare:82 | ||||
| chr17:8495135-8495370 | Common:1; Rare:49 | ||||
| chr17:8508563-8508774 | Rare:53 | ||||
| chr17:8512568-8512882 | Common:2; Rare:53 | ||||
| chr17:8513757-8513805 | Rare:10 | ||||
| chr17:8513809-8513955 | Rare:26 | ||||
| chr17:8965058-8965098 | Rare:6 | ||||
| chr17:16061732-16062030 | Common:1; Rare:82 | ||||
| chr17:16439350-16439723 | Common:6; Rare:145 | ||||
| chr17:16439977-16440251 | Rare:113 | ||||
| chr17:17805830-17806071 | Common:3; Rare:55 | ||||
| chr17:17826136-17826247 | Rare:13 | ||||
| chr17:17836137-17836433 | Common:3; Rare:74 |