| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:29148942-29149119 | Common:1; Rare:42 | ||||
| chr17:30600105-30600428 | Common:5; Rare:63 | ||||
| chr17:30731412-30731699 | Common:3; Rare:83 | ||||
| chr17:35254468-35254736 | Common:2; Rare:48 | ||||
| chr17:35567924-35568210 | Common:2; Rare:78 | ||||
| chr17:37717247-37717388 | Common:1; Rare:29 | ||||
| chr17:38702311-38702479 | Rare:57 | ||||
| chr17:38867492-38867645 | Common:4; Rare:53 | ||||
| chr17:39056934-39057066 | Common:5; Rare:38 | ||||
| chr17:40223883-40223902 | Rare:3 | ||||
| chr17:40416403-40416897 | Rare:82; Clinvar (benign):1 | ||||
| chr17:41678725-41678871 | Common:1; Rare:36 | ||||
| chr17:42678316-42678591 | Common:1; Rare:50 | ||||
| chr17:43315627-43315930 | Common:8; Rare:133 | ||||
| chr17:43368056-43368454 | Common:12; Rare:154 |