| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13017602-13017702 | Rare:39 | ||||
| chr17:13017932-13018339 | Common:7; Rare:137; Clinvar (benign):2 | ||||
| chr17:14069349-14069593 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14300778-14301105 | Common:2; Rare:87 | ||||
| chr17:15260756-15260951 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr17:15563435-15563731 | Rare:102 | ||||
| chr17:15684283-15684343 | Common:1; Rare:21 | ||||
| chr17:15699500-15699797 | Common:3; Rare:79 | ||||
| chr17:15999578-15999971 | Common:3; Rare:180; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:16215530-16215657 | Common:1; Rare:52 | ||||
| chr17:16217094-16217253 | Rare:55; Clinvar:1 | ||||
| chr17:16380577-16380829 | Common:4; Rare:66 | ||||
| chr17:17237143-17237438 | Common:4; Rare:88; Clinvar (benign):2 | ||||
| chr17:17281194-17281308 | Rare:56 | ||||
| chr17:17496388-17496538 | Rare:36 |