| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636225-3636496 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr17:3668538-3668863 | Common:3; Rare:135 | ||||
| chr17:3723752-3723917 | Common:1; Rare:90 | ||||
| chr17:4142989-4143250 | Rare:92 | ||||
| chr17:4143597-4143741 | Common:4; Rare:81 | ||||
| chr17:4263943-4264031 | Rare:38 | ||||
| chr17:4366469-4366778 | Common:1; Rare:124 | ||||
| chr17:4555329-4555503 | Common:3; Rare:80 | ||||
| chr17:4704097-4704216 | Rare:65 | ||||
| chr17:4731295-4731481 | Common:2; Rare:54 | ||||
| chr17:4796031-4796266 | Common:2; Rare:90 | ||||
| chr17:4806987-4807192 | Common:4; Rare:66 | ||||
| chr17:4833128-4833529 | Rare:108 | ||||
| chr17:4939907-4940391 | Common:2; Rare:143 | ||||
| chr17:4948386-4948710 | Common:4; Rare:133 |