| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303717-2303987 | Common:2; Rare:103 | ||||
| chr17:2336430-2336589 | Rare:62 | ||||
| chr17:2337346-2337631 | Common:1; Rare:86 | ||||
| chr17:2401042-2401238 | Rare:61 | ||||
| chr17:2511774-2512021 | Common:2; Rare:73 | ||||
| chr17:2593445-2593669 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr17:2593863-2593998 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711767-2712038 | Common:2; Rare:74 | ||||
| chr17:2776608-2776875 | Common:5; Rare:82 | ||||
| chr17:3557797-3557950 | Common:4; Rare:29; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:3636241-3636517 | Common:4; Rare:78; Clinvar (benign):1 | ||||
| chr17:3668552-3668837 | Common:2; Rare:112 | ||||
| chr17:3695788-3695840 | Common:1; Rare:20 | ||||
| chr17:3723756-3723938 | Common:1; Rare:104 | ||||
| chr17:3845904-3846042 | Rare:35 |