| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4739798-4739845 | Rare:6 | ||||
| chr17:4786295-4786512 | Rare:61 | ||||
| chr17:4795993-4796318 | Common:2; Rare:110 | ||||
| chr17:4796697-4796830 | Common:1; Rare:42 | ||||
| chr17:4806928-4807217 | Common:4; Rare:91 | ||||
| chr17:4833171-4833434 | Rare:78 | ||||
| chr17:4833797-4833908 | Rare:18 | ||||
| chr17:4899330-4899717 | Common:3; Rare:196; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr17:4939863-4940423 | Common:2; Rare:161 | ||||
| chr17:4940494-4940698 | Common:2; Rare:62 | ||||
| chr17:4941208-4941428 | Common:2; Rare:43 | ||||
| chr17:4947008-4947252 | Common:2; Rare:61 | ||||
| chr17:4947500-4947861 | Common:4; Rare:121 | ||||
| chr17:4947867-4948137 | Common:1; Rare:86 | ||||
| chr17:4948425-4948847 | Common:5; Rare:155 |