| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1716152-1716597 | Common:4; Rare:145 | ||||
| chr17:1724651-1724716 | Rare:23 | ||||
| chr17:1829780-1830126 | Common:9; Rare:144 | ||||
| chr17:2303493-2303657 | Rare:58 | ||||
| chr17:2303703-2304014 | Common:2; Rare:116 | ||||
| chr17:2335657-2336535 | Rare:304 | ||||
| chr17:2337378-2337512 | Rare:41 | ||||
| chr17:2394053-2394240 | Common:1; Rare:68 | ||||
| chr17:2396763-2397021 | Common:2; Rare:51 | ||||
| chr17:2511775-2512018 | Common:2; Rare:73 | ||||
| chr17:2593407-2593664 | Common:4; Rare:97 | ||||
| chr17:2593730-2594001 | Common:1; Rare:66; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:2711721-2712032 | Common:2; Rare:88 | ||||
| chr17:3636241-3636501 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr17:3636655-3636775 | Common:1; Rare:29; Clinvar:2; Clinvar (benign):1 |