| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13017967-13018287 | Common:6; Rare:96; Clinvar (benign):1 | ||||
| chr17:14069395-14069580 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15563549-15563755 | Common:1; Rare:56 | ||||
| chr17:15684226-15684334 | Common:3; Rare:38 | ||||
| chr17:15699484-15699797 | Common:3; Rare:85 | ||||
| chr17:15999605-16000032 | Common:3; Rare:182; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217102-16217227 | Rare:31 | ||||
| chr17:16380561-16380820 | Common:4; Rare:69 | ||||
| chr17:16381011-16381180 | Common:3; Rare:80 | ||||
| chr17:16569140-16569322 | Common:1; Rare:60 | ||||
| chr17:17281194-17281379 | Rare:76 | ||||
| chr17:17476828-17477054 | Common:3; Rare:63 | ||||
| chr17:17496392-17496493 | Rare:25 | ||||
| chr17:17591589-17591932 | Common:2; Rare:98 | ||||
| chr17:17836809-17837074 | Common:3; Rare:64 |