| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2337361-2337631 | Common:1; Rare:80 | ||||
| chr17:2511785-2512021 | Common:2; Rare:72 | ||||
| chr17:2593464-2593709 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2593857-2593996 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711783-2712038 | Common:2; Rare:68 | ||||
| chr17:2777156-2777246 | Rare:17 | ||||
| chr17:3636275-3636508 | Common:4; Rare:55; Clinvar (benign):1 | ||||
| chr17:3636683-3636772 | Common:1; Rare:23; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668552-3668828 | Common:2; Rare:107 | ||||
| chr17:3723762-3723938 | Common:1; Rare:102 | ||||
| chr17:4142982-4143250 | Rare:93 | ||||
| chr17:4143597-4143768 | Common:4; Rare:102 | ||||
| chr17:4263943-4264037 | Rare:41 | ||||
| chr17:4555304-4555518 | Common:3; Rare:99 | ||||
| chr17:4704110-4704260 | Rare:80 |