| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16217084-16217332 | Rare:186; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr17:16353375-16353567 | Rare:72 | ||||
| chr17:16380580-16381195 | Common:18; Rare:410 | ||||
| chr17:16491994-16492600 | Common:11; Rare:378 | ||||
| chr17:16653701-16653861 | Common:1; Rare:51 | ||||
| chr17:17042196-17042580 | Common:60; Rare:356 | ||||
| chr17:17205785-17206899 | Common:13; Rare:693 | ||||
| chr17:17236577-17236986 | Common:2; Rare:129; Clinvar (benign):1 | ||||
| chr17:17237062-17237747 | Common:20; Rare:465; Clinvar:2; Clinvar (benign):8 | ||||
| chr17:17280640-17280910 | Common:7; Rare:188 | ||||
| chr17:17281157-17281427 | Rare:250 | ||||
| chr17:17303069-17303419 | Common:10; Rare:230 | ||||
| chr17:17303558-17303692 | Rare:89 | ||||
| chr17:17303722-17303852 | Rare:83 | ||||
| chr17:17476858-17477096 | Common:6; Rare:121 |