| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8436359-8436460 | Common:1; Rare:15 | ||||
| chr17:8436537-8436653 | Common:1; Rare:18 | ||||
| chr17:8630643-8631212 | Common:4; Rare:182 | ||||
| chr17:9021132-9021323 | Common:1; Rare:50 | ||||
| chr17:9021352-9021559 | Common:2; Rare:77 | ||||
| chr17:9575708-9575966 | Common:8; Rare:73 | ||||
| chr17:9644545-9644809 | Common:2; Rare:44 | ||||
| chr17:9645180-9645414 | Common:1; Rare:44 | ||||
| chr17:10114531-10114762 | Common:1; Rare:38 | ||||
| chr17:10115021-10115342 | Common:3; Rare:79 | ||||
| chr17:10198467-10198721 | Common:3; Rare:71 | ||||
| chr17:10697377-10697420 | Rare:18; Clinvar (benign):1 | ||||
| chr17:10697472-10697777 | Common:6; Rare:125; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:10698541-10698574 | Rare:11 | ||||
| chr17:10729692-10729796 | Rare:45 |