| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:14069440-14069539 | Common:1; Rare:32; Clinvar (benign):2 | ||||
| chr17:14300806-14301088 | Common:1; Rare:77 | ||||
| chr17:15563439-15563722 | Rare:98 | ||||
| chr17:15684273-15684348 | Common:1; Rare:27 | ||||
| chr17:15699510-15699789 | Common:3; Rare:74 | ||||
| chr17:15999578-16000003 | Common:3; Rare:186; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:17281198-17281365 | Rare:64 | ||||
| chr17:17591582-17591926 | Common:2; Rare:97 | ||||
| chr17:18087781-18088015 | Rare:66 | ||||
| chr17:18225355-18225661 | Common:3; Rare:98 | ||||
| chr17:18314911-18315326 | Common:1; Rare:116 | ||||
| chr17:18363393-18363742 | Common:6; Rare:113 | ||||
| chr17:18682211-18682479 | Common:9; Rare:26 | ||||
| chr17:18781076-18781318 | Common:5; Rare:68 | ||||
| chr17:18856149-18856380 | Common:1; Rare:45 |