| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40287586-40287986 | Rare:104 | ||||
| chr17:40318085-40318315 | Common:1; Rare:53 | ||||
| chr17:40342038-40342399 | Common:1; Rare:79 | ||||
| chr17:40417692-40418113 | Rare:116 | ||||
| chr17:40665122-40665184 | Common:1; Rare:33 | ||||
| chr17:40822592-40822620 | Rare:7 | ||||
| chr17:40937412-40937703 | Common:6; Rare:47 | ||||
| chr17:41351305-41351511 | Common:3; Rare:38 | ||||
| chr17:41521873-41522065 | Common:1; Rare:23 | ||||
| chr17:41688613-41689064 | Common:3; Rare:180 | ||||
| chr17:41689287-41689565 | Common:3; Rare:104 | ||||
| chr17:41734640-41734910 | Common:5; Rare:56 | ||||
| chr17:41786664-41787105 | Common:3; Rare:113; Clinvar (benign):1 | ||||
| chr17:41812617-41813022 | Common:3; Rare:91; Clinvar:5 | ||||
| chr17:41835088-41835170 | Rare:26 |