| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2593818-2593984 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711762-2712031 | Common:2; Rare:75 | ||||
| chr17:3636241-3636479 | Common:4; Rare:63; Clinvar (benign):1 | ||||
| chr17:3668552-3668861 | Common:2; Rare:126 | ||||
| chr17:3723767-3723922 | Common:1; Rare:87 | ||||
| chr17:3845922-3846040 | Rare:32 | ||||
| chr17:3892950-3893242 | Common:3; Rare:101 | ||||
| chr17:4142978-4143244 | Rare:92 | ||||
| chr17:4143597-4143740 | Common:4; Rare:80 | ||||
| chr17:4263937-4264026 | Rare:39 | ||||
| chr17:4704107-4704260 | Rare:80 | ||||
| chr17:4739542-4739617 | Rare:22 | ||||
| chr17:4739628-4739914 | Common:3; Rare:66 | ||||
| chr17:4806996-4807192 | Common:4; Rare:65 | ||||
| chr17:4939916-4940017 | Rare:35 |