| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44947705-44947877 | Common:1; Rare:48 | ||||
| chr17:45051453-45051688 | Common:1; Rare:84 | ||||
| chr17:45060987-45061393 | Common:2; Rare:122 | ||||
| chr17:45132380-45132639 | Common:1; Rare:79 | ||||
| chr17:45148165-45148615 | Common:1; Rare:158 | ||||
| chr17:45148702-45149020 | Common:2; Rare:84 | ||||
| chr17:45161494-45161721 | Rare:57 | ||||
| chr17:45395815-45395909 | Rare:33 | ||||
| chr17:45490708-45490863 | Rare:54 | ||||
| chr17:46192858-46192991 | Common:1; Rare:34 | ||||
| chr17:46193330-46193636 | Common:6; Rare:90 | ||||
| chr17:46922841-46923204 | Common:5; Rare:109; Clinvar:3; Clinvar (benign):8 | ||||
| chr17:47189246-47189321 | Rare:23 | ||||
| chr17:47323890-47324025 | Common:1; Rare:44 | ||||
| chr17:47530944-47531290 | Common:1; Rare:95 |