| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1516487-1516984 | Common:4; Rare:180 | ||||
| chr17:1673474-1673777 | Rare:81 | ||||
| chr17:1684780-1685048 | Common:2; Rare:87; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716186-1716536 | Common:3; Rare:110 | ||||
| chr17:1730262-1730526 | Common:1; Rare:79 | ||||
| chr17:1762656-1762856 | Common:4; Rare:47 | ||||
| chr17:1829428-1829549 | Rare:30 | ||||
| chr17:1829762-1830083 | Common:8; Rare:134 | ||||
| chr17:2172805-2173079 | Common:1; Rare:60 | ||||
| chr17:2303461-2303633 | Rare:63 | ||||
| chr17:2303709-2304001 | Common:2; Rare:112 | ||||
| chr17:2336415-2336537 | Rare:50 | ||||
| chr17:2337250-2337642 | Common:1; Rare:110 | ||||
| chr17:2392644-2392850 | Common:4; Rare:86 | ||||
| chr17:2396780-2397047 | Common:2; Rare:63 |