| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17591595-17591952 | Common:1; Rare:103 | ||||
| chr17:18087861-18088026 | Rare:47 | ||||
| chr17:18183771-18183931 | Rare:69 | ||||
| chr17:18225352-18225661 | Common:3; Rare:98 | ||||
| chr17:18246982-18247194 | Common:8; Rare:121 | ||||
| chr17:18247296-18247566 | Common:3; Rare:78 | ||||
| chr17:18254520-18254824 | Rare:104 | ||||
| chr17:18258686-18258835 | Common:1; Rare:42 | ||||
| chr17:18314921-18315332 | Common:1; Rare:117 | ||||
| chr17:18363399-18363712 | Common:5; Rare:105 | ||||
| chr17:18682211-18682479 | Common:9; Rare:26 | ||||
| chr17:18781121-18781318 | Common:3; Rare:56 | ||||
| chr17:18856152-18856375 | Common:1; Rare:40 | ||||
| chr17:18857873-18858208 | Common:6; Rare:78 | ||||
| chr17:19362575-19362804 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):2 |