| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4807019-4807192 | Common:4; Rare:59 | ||||
| chr17:4939885-4940373 | Common:2; Rare:146 | ||||
| chr17:4943220-4943501 | Common:1; Rare:99 | ||||
| chr17:4948929-4949055 | Common:1; Rare:41 | ||||
| chr17:4949857-4950171 | Common:1; Rare:72 | ||||
| chr17:4967742-4967976 | Rare:96 | ||||
| chr17:4987049-4987172 | Rare:33 | ||||
| chr17:4987640-4987819 | Common:1; Rare:62 | ||||
| chr17:4997892-4998154 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr17:5007067-5007284 | Rare:53; Clinvar:1 | ||||
| chr17:5035387-5035440 | Rare:16 | ||||
| chr17:5078425-5078531 | Common:1; Rare:33 | ||||
| chr17:5191838-5192077 | Common:1; Rare:79 | ||||
| chr17:5234804-5234937 | Rare:34 | ||||
| chr17:5419628-5419882 | Common:3; Rare:81 |