| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50169382-50169706 | Common:3; Rare:62 | ||||
| chr17:50178215-50178623 | Common:4; Rare:104 | ||||
| chr17:50289900-50290430 | Common:1; Rare:78 | ||||
| chr17:50427345-50427606 | Rare:36 | ||||
| chr17:50542078-50542328 | Common:1; Rare:89 | ||||
| chr17:50626226-50626338 | Rare:31; Clinvar:1 | ||||
| chr17:50630620-50630860 | Common:2; Rare:38 | ||||
| chr17:50635689-50635822 | Common:2; Rare:17 | ||||
| chr17:50639323-50639572 | Common:2; Rare:41 | ||||
| chr17:50681451-50681580 | Rare:25 | ||||
| chr17:50684808-50685014 | Rare:52 | ||||
| chr17:50686310-50686550 | Common:1; Rare:42 | ||||
| chr17:50686571-50686707 | Rare:21 | ||||
| chr17:50768220-50768520 | Common:3; Rare:53 | ||||
| chr17:50783213-50783467 | Common:3; Rare:51 |