| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:714627-714982 | Common:5; Rare:118; Clinvar (benign):3 | ||||
| chr17:732239-732627 | Common:2; Rare:129 | ||||
| chr17:752138-752308 | Common:2; Rare:73 | ||||
| chr17:752759-752902 | Rare:32 | ||||
| chr17:979706-979994 | Common:4; Rare:139 | ||||
| chr17:1010856-1010930 | Rare:25 | ||||
| chr17:1050981-1051085 | Rare:18 | ||||
| chr17:1092022-1092129 | Rare:27 | ||||
| chr17:1092160-1092318 | Common:2; Rare:27 | ||||
| chr17:1400048-1400294 | Common:2; Rare:93 | ||||
| chr17:1400353-1400380 | Rare:15 | ||||
| chr17:1456101-1456434 | Common:2; Rare:132 | ||||
| chr17:1468407-1468649 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr17:1470491-1470715 | Common:1; Rare:94 | ||||
| chr17:1480533-1480878 | Common:2; Rare:118; Clinvar (benign):2 |