| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40140715-40140747 | Rare:14 | ||||
| chr17:40318033-40318293 | Common:1; Rare:54 | ||||
| chr17:40417846-40418186 | Rare:104 | ||||
| chr17:41688640-41688893 | Common:1; Rare:81 | ||||
| chr17:41689287-41689604 | Common:3; Rare:116 | ||||
| chr17:41812621-41812710 | Common:3; Rare:15 | ||||
| chr17:41812841-41813029 | Rare:50; Clinvar:2 | ||||
| chr17:41966606-41966874 | Common:1; Rare:96 | ||||
| chr17:42017367-42017486 | Rare:53 | ||||
| chr17:42017524-42017701 | Rare:50 | ||||
| chr17:42423144-42423436 | Common:1; Rare:75; Clinvar:2 | ||||
| chr17:42458738-42458914 | Common:1; Rare:70 | ||||
| chr17:42566955-42567151 | Common:3; Rare:66 | ||||
| chr17:42577631-42577825 | Rare:88 | ||||
| chr17:42609328-42609732 | Common:8; Rare:170; Clinvar (benign):2 |