| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699489-15699768 | Common:3; Rare:74 | ||||
| chr17:15999598-16000025 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217198-16217238 | Rare:18; Clinvar:1 | ||||
| chr17:16415692-16415811 | Common:1; Rare:35 | ||||
| chr17:16972071-16972195 | Rare:28 | ||||
| chr17:17237390-17237693 | Common:4; Rare:68 | ||||
| chr17:17281182-17281376 | Rare:77 | ||||
| chr17:17476714-17477054 | Common:4; Rare:78 | ||||
| chr17:17591604-17591948 | Common:1; Rare:99 | ||||
| chr17:17823586-17823845 | Common:5; Rare:116 | ||||
| chr17:18087783-18088005 | Rare:62 | ||||
| chr17:18183023-18183111 | Rare:30 | ||||
| chr17:18258694-18258815 | Common:1; Rare:38 | ||||
| chr17:18314921-18315348 | Common:1; Rare:123 | ||||
| chr17:18363393-18363705 | Common:5; Rare:102 |