| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:67366475-67366742 | Rare:89 | ||||
| chr17:67377256-67377484 | Common:2; Rare:63 | ||||
| chr17:67378784-67378988 | Common:1; Rare:58 | ||||
| chr17:67717759-67717959 | Rare:70 | ||||
| chr17:67826246-67826255 | Rare:1 | ||||
| chr17:68043049-68043171 | Rare:50 | ||||
| chr17:68247802-68248142 | Common:6; Rare:150 | ||||
| chr17:68258977-68259210 | Common:1; Rare:68 | ||||
| chr17:68291221-68291568 | Common:2; Rare:100 | ||||
| chr17:68346504-68346582 | Rare:13 | ||||
| chr17:68346644-68346829 | Common:1; Rare:41 | ||||
| chr17:68511718-68512081 | Rare:101 | ||||
| chr17:68512287-68512548 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:68515126-68515570 | Common:3; Rare:119; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr17:68600517-68600579 | Rare:23 |