| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699521-15699773 | Common:3; Rare:68 | ||||
| chr17:15999566-16000028 | Common:3; Rare:195; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039549-16039769 | Common:1; Rare:55 | ||||
| chr17:16215371-16215657 | Common:2; Rare:115 | ||||
| chr17:16217115-16217247 | Rare:44; Clinvar:1 | ||||
| chr17:16380572-16380806 | Common:4; Rare:58 | ||||
| chr17:16415685-16415827 | Common:1; Rare:41 | ||||
| chr17:17237123-17237438 | Common:4; Rare:99; Clinvar (benign):2 | ||||
| chr17:17496370-17496530 | Rare:39 | ||||
| chr17:17506392-17506619 | Common:2; Rare:50 | ||||
| chr17:17591589-17591932 | Common:2; Rare:98 | ||||
| chr17:17812755-17813058 | Common:1; Rare:83 | ||||
| chr17:17815409-17815512 | Common:1; Rare:22 | ||||
| chr17:17823559-17823825 | Common:5; Rare:130 | ||||
| chr17:18039095-18039375 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):1 |