| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:81395040-81395513 | Common:5; Rare:448 | ||||
| chr17:81398986-81399623 | Common:36; Rare:469 | ||||
| chr17:81399660-81400528 | Common:32; Rare:966 | ||||
| chr17:81400450-81400940 | Common:9; Rare:348 | ||||
| chr17:81511368-81512053 | Common:6; Rare:419; Clinvar:6; Clinvar (benign):34; Clinvar (pathogenic):3 | ||||
| chr17:81512712-81513180 | Common:36; Rare:1012; Clinvar (benign):54 | ||||
| chr17:81514589-81515125 | Common:3; Rare:506 | ||||
| chr17:81551937-81552178 | Rare:73 | ||||
| chr17:81552080-81552260 | Rare:48 | ||||
| chr17:81552260-81552741 | Common:6; Rare:490 | ||||
| chr17:81553066-81553444 | Common:6; Rare:233 | ||||
| chr17:81553571-81553971 | Common:1; Rare:109 | ||||
| chr17:81629580-81629880 | Common:2; Rare:84 | ||||
| chr17:81636708-81637302 | Common:19; Rare:717 | ||||
| chr17:81663042-81663762 | Common:78; Rare:852 |