| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6651559-6651727 | Common:1; Rare:60 | ||||
| chr17:7012326-7012713 | Rare:127 | ||||
| chr17:7242230-7242616 | Common:1; Rare:116 | ||||
| chr17:7242897-7243136 | Common:1; Rare:105 | ||||
| chr17:7251948-7252311 | Common:2; Rare:144 | ||||
| chr17:7484132-7484371 | Common:1; Rare:83 | ||||
| chr17:7583508-7583877 | Common:1; Rare:146; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7627802-7627962 | Common:2; Rare:54 | ||||
| chr17:7687538-7687569 | Rare:9 | ||||
| chr17:7857467-7858093 | Common:4; Rare:202 | ||||
| chr17:7931898-7932241 | Common:5; Rare:93 | ||||
| chr17:10697503-10697648 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:13601928-13602184 | Common:1; Rare:78 | ||||
| chr17:15260808-15260912 | Rare:41 | ||||
| chr17:15999579-15999851 | Common:3; Rare:138; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 |