| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41663427-41663755 | Common:2; Rare:54 | ||||
| chr17:41752251-41752536 | Common:2; Rare:66 | ||||
| chr17:41756775-41756860 | Common:2; Rare:11 | ||||
| chr17:41758587-41758875 | Common:2; Rare:69; Clinvar:12; Clinvar (benign):6 | ||||
| chr17:41764409-41764819 | Common:2; Rare:78; Clinvar:4 | ||||
| chr17:41768811-41768912 | Common:1; Rare:18 | ||||
| chr17:41768920-41769686 | Common:5; Rare:250; Clinvar:36; Clinvar (benign):26; Clinvar (pathogenic):2 | ||||
| chr17:41770348-41770428 | Rare:17 | ||||
| chr17:41775131-41775442 | Common:1; Rare:48 | ||||
| chr17:41775499-41775584 | Common:1; Rare:14 | ||||
| chr17:41781680-41781847 | Rare:28 | ||||
| chr17:41782125-41782274 | Common:1; Rare:32 | ||||
| chr17:41784167-41784418 | Common:2; Rare:62 | ||||
| chr17:41793230-41793499 | Common:3; Rare:58 | ||||
| chr17:41983603-41983859 | Rare:44 |