| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59707388-59707732 | Common:3; Rare:96; Clinvar (benign):4 | ||||
| chr17:59837635-59837970 | Rare:48 | ||||
| chr17:59892895-59893149 | Rare:75 | ||||
| chr17:60392019-60392325 | Common:2; Rare:76 | ||||
| chr17:60526211-60526290 | Rare:27 | ||||
| chr17:63827086-63827492 | Common:5; Rare:115 | ||||
| chr17:65056592-65056919 | Common:4; Rare:133 | ||||
| chr17:67717838-67717959 | Rare:51 | ||||
| chr17:68247813-68248147 | Common:6; Rare:146 | ||||
| chr17:73232226-73232706 | Common:3; Rare:172 | ||||
| chr17:73311963-73312184 | Rare:57 | ||||
| chr17:74776281-74776543 | Common:4; Rare:87 | ||||
| chr17:75012536-75012712 | Common:2; Rare:49 | ||||
| chr17:75130807-75131084 | Common:2; Rare:99 | ||||
| chr17:75205380-75205709 | Common:1; Rare:88 |