| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89686560-89686704 | Common:6; Rare:63 | ||||
| chr16:89972521-89972648 | Rare:47 | ||||
| chr16:90022533-90022709 | Rare:69 | ||||
| chr17:714799-714883 | Common:1; Rare:31 | ||||
| chr17:752247-752333 | Common:1; Rare:28 | ||||
| chr17:752794-752879 | Rare:22 | ||||
| chr17:1516628-1516945 | Rare:108 | ||||
| chr17:1770244-1770378 | Common:1; Rare:28 | ||||
| chr17:1829826-1829985 | Common:3; Rare:69 | ||||
| chr17:2303504-2303637 | Rare:48 | ||||
| chr17:2303774-2303980 | Common:2; Rare:75 | ||||
| chr17:2336430-2336540 | Rare:42 | ||||
| chr17:2511853-2511926 | Common:2; Rare:16 | ||||
| chr17:2593490-2593658 | Common:2; Rare:62 | ||||
| chr17:3636246-3636468 | Common:4; Rare:58; Clinvar (benign):1 |