| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:732311-732607 | Common:1; Rare:103 | ||||
| chr17:752149-752378 | Common:3; Rare:91 | ||||
| chr17:782466-782691 | Common:1; Rare:81 | ||||
| chr17:979721-979987 | Common:3; Rare:128 | ||||
| chr17:1109034-1109221 | Common:1; Rare:70 | ||||
| chr17:1400024-1400273 | Common:2; Rare:100 | ||||
| chr17:1455976-1456049 | Rare:18 | ||||
| chr17:1456158-1456458 | Common:4; Rare:113 | ||||
| chr17:1478443-1478730 | Common:1; Rare:114; Clinvar (benign):1 | ||||
| chr17:1491609-1491775 | Common:1; Rare:49 | ||||
| chr17:1516576-1517033 | Common:2; Rare:157 | ||||
| chr17:1628782-1628912 | Rare:45 | ||||
| chr17:1651338-1651785 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1675962-1676314 | Common:1; Rare:64; Clinvar (benign):4 | ||||
| chr17:1684289-1684460 | Common:3; Rare:68 |