| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:67244493-67244831 | Rare:101 | ||||
| chr17:67245147-67245321 | Rare:54 | ||||
| chr17:67366407-67366708 | Common:1; Rare:98 | ||||
| chr17:67717662-67717966 | Common:2; Rare:103 | ||||
| chr17:68035372-68035912 | Common:5; Rare:125 | ||||
| chr17:68035937-68035994 | Rare:13 | ||||
| chr17:68247860-68248142 | Common:6; Rare:118 | ||||
| chr17:68291293-68291566 | Common:2; Rare:81 | ||||
| chr17:68511765-68512136 | Common:1; Rare:96 | ||||
| chr17:68512326-68512574 | Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:68512681-68512973 | Rare:107 | ||||
| chr17:68514887-68515095 | Common:1; Rare:54 | ||||
| chr17:68515105-68515573 | Common:3; Rare:124; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr17:68558372-68558543 | Common:1; Rare:36 | ||||
| chr17:68601361-68601711 | Common:5; Rare:93 |