| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4806996-4807192 | Common:4; Rare:65 | ||||
| chr17:4899344-4899549 | Common:2; Rare:126; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:4939881-4940373 | Common:2; Rare:147 | ||||
| chr17:4948144-4948240 | Rare:31 | ||||
| chr17:4948386-4948710 | Common:4; Rare:133 | ||||
| chr17:4948921-4949197 | Common:2; Rare:92 | ||||
| chr17:4950462-4950577 | Rare:24 | ||||
| chr17:4967154-4967417 | Common:2; Rare:61 | ||||
| chr17:4967743-4967860 | Rare:54 | ||||
| chr17:4967912-4967976 | Rare:24 | ||||
| chr17:4987640-4987761 | Rare:48 | ||||
| chr17:4997873-4998145 | Common:2; Rare:110; Clinvar (benign):1 | ||||
| chr17:5191838-5192116 | Common:2; Rare:88 | ||||
| chr17:5234788-5234976 | Rare:44 | ||||
| chr17:5419577-5419828 | Common:3; Rare:100 |