| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39461844-39462015 | Common:6; Rare:70 | ||||
| chr17:39637029-39637216 | Common:6; Rare:115 | ||||
| chr17:39637240-39637570 | Common:3; Rare:91 | ||||
| chr17:39687630-39687940 | Rare:169; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:39688016-39688197 | Rare:57 | ||||
| chr17:39699898-39700093 | Rare:83 | ||||
| chr17:39730402-39730629 | Common:1; Rare:80 | ||||
| chr17:39737545-39737779 | Rare:92 | ||||
| chr17:39737822-39738008 | Rare:53 | ||||
| chr17:39738243-39738364 | Rare:30 | ||||
| chr17:39738265-39738378 | Rare:26 | ||||
| chr17:39739104-39739752 | Common:5; Rare:273 | ||||
| chr17:39742369-39742594 | Common:1; Rare:72 | ||||
| chr17:39924160-39924620 | Common:2; Rare:155 | ||||
| chr17:39926921-39927078 | Rare:58 |