| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1661673-1661991 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:1710342-1710483 | Rare:37 | ||||
| chr17:1716192-1716563 | Common:4; Rare:120 | ||||
| chr17:1730262-1730520 | Common:1; Rare:78 | ||||
| chr17:1742687-1743033 | Common:1; Rare:75 | ||||
| chr17:1762685-1762859 | Common:3; Rare:47 | ||||
| chr17:1829770-1830082 | Common:8; Rare:133 | ||||
| chr17:2303458-2303587 | Rare:46 | ||||
| chr17:2303728-2303987 | Common:2; Rare:97 | ||||
| chr17:2336398-2336543 | Rare:66 | ||||
| chr17:2337381-2337631 | Common:1; Rare:70 | ||||
| chr17:2511806-2511966 | Common:2; Rare:47 | ||||
| chr17:2593482-2593658 | Common:2; Rare:65 | ||||
| chr17:2593857-2593987 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711762-2712031 | Common:2; Rare:75 |