| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57988180-57988541 | Common:5; Rare:106 | ||||
| chr17:58007183-58007384 | Common:1; Rare:92 | ||||
| chr17:58219220-58219387 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58279428-58279603 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr17:58352131-58352458 | Common:6; Rare:130 | ||||
| chr17:58692486-58692709 | Common:2; Rare:115; Clinvar:21; Clinvar (benign):20 | ||||
| chr17:59106695-59107094 | Common:2; Rare:135; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:59155120-59155784 | Common:2; Rare:170 | ||||
| chr17:59565451-59565676 | Common:1; Rare:86 | ||||
| chr17:59619541-59620025 | Common:3; Rare:171 | ||||
| chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr17:59892891-59893170 | Common:1; Rare:83 | ||||
| chr17:59964719-59964842 | Common:2; Rare:54 | ||||
| chr17:60078917-60078971 | Common:4; Rare:29 | ||||
| chr17:60526177-60526293 | Rare:48 |