| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:10697487-10697653 | Common:3; Rare:73; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:10729775-10729801 | Rare:11 | ||||
| chr17:12021354-12021681 | Rare:89 | ||||
| chr17:12665875-12666209 | Common:2; Rare:76 | ||||
| chr17:13017581-13017828 | Common:1; Rare:99; Clinvar (benign):3 | ||||
| chr17:13017960-13018341 | Common:7; Rare:123; Clinvar (benign):2 | ||||
| chr17:14069349-14069593 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14300814-14301148 | Common:3; Rare:92 | ||||
| chr17:15260755-15260982 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr17:15262472-15262735 | Rare:58 | ||||
| chr17:15636015-15636063 | Rare:15 | ||||
| chr17:15999510-15999859 | Common:3; Rare:175; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:15999860-16000134 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:16058212-16058591 | Common:1; Rare:84 | ||||
| chr17:16080318-16080478 | Common:1; Rare:34 |