| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4366643-4366848 | Common:1; Rare:76 | ||||
| chr17:4433609-4433982 | Common:2; Rare:81 | ||||
| chr17:4704104-4704296 | Rare:98 | ||||
| chr17:4899525-4899659 | Common:1; Rare:49; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:4939916-4940390 | Common:2; Rare:139 | ||||
| chr17:4948933-4949185 | Common:2; Rare:86 | ||||
| chr17:4967797-4968003 | Common:1; Rare:74 | ||||
| chr17:5116367-5116507 | Common:2; Rare:30 | ||||
| chr17:5191837-5192077 | Common:1; Rare:79 | ||||
| chr17:5282043-5282336 | Common:12; Rare:150 | ||||
| chr17:5420121-5420202 | Rare:32 | ||||
| chr17:5486157-5486608 | Common:5; Rare:152 | ||||
| chr17:5486815-5486920 | Common:3; Rare:33 | ||||
| chr17:6640646-6641082 | Common:7; Rare:133 | ||||
| chr17:6651455-6651737 | Common:1; Rare:100 |