| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13017960-13018333 | Common:7; Rare:120; Clinvar (benign):2 | ||||
| chr17:14069393-14069608 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:14300790-14301105 | Common:2; Rare:85 | ||||
| chr17:15260684-15261066 | Common:3; Rare:120; Clinvar (benign):5 | ||||
| chr17:15262431-15262738 | Rare:67 | ||||
| chr17:15475726-15475923 | Common:1; Rare:37 | ||||
| chr17:15699521-15699785 | Common:3; Rare:72 | ||||
| chr17:15999586-16000028 | Common:3; Rare:187; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039579-16039777 | Common:1; Rare:45 | ||||
| chr17:16215522-16215657 | Common:1; Rare:53 | ||||
| chr17:16217102-16217240 | Rare:40; Clinvar:1 | ||||
| chr17:17281143-17281379 | Rare:91 | ||||
| chr17:17495616-17495906 | Common:1; Rare:77 | ||||
| chr17:17496129-17496240 | Rare:38 | ||||
| chr17:17496384-17496532 | Rare:37 |