| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30906200-30906354 | Common:1; Rare:46 | ||||
| chr17:31314006-31314281 | Rare:49 | ||||
| chr17:31321579-31321876 | Common:3; Rare:49 | ||||
| chr17:31901653-31901956 | Common:2; Rare:95 | ||||
| chr17:32350012-32350209 | Rare:103 | ||||
| chr17:32876781-32876840 | Rare:19 | ||||
| chr17:32876844-32876981 | Rare:47 | ||||
| chr17:33293264-33293352 | Rare:25 | ||||
| chr17:34961456-34961575 | Common:1; Rare:58 | ||||
| chr17:34961895-34962181 | Common:1; Rare:108 | ||||
| chr17:34980390-34980618 | Common:4; Rare:67 | ||||
| chr17:34981123-34981283 | Common:2; Rare:26 | ||||
| chr17:35242901-35243081 | Rare:59 | ||||
| chr17:35373609-35373751 | Common:2; Rare:32 | ||||
| chr17:35578539-35578707 | Common:1; Rare:44; Clinvar (benign):1 |