| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7997251-7997434 | Rare:31 | ||||
| chr17:8006040-8006290 | Common:3; Rare:34 | ||||
| chr17:8016729-8016848 | Common:1; Rare:19 | ||||
| chr17:8060137-8060442 | Common:4; Rare:64 | ||||
| chr17:8120317-8120504 | Common:3; Rare:104 | ||||
| chr17:8120814-8120993 | Common:5; Rare:118 | ||||
| chr17:8122004-8122156 | Rare:45 | ||||
| chr17:8126450-8126798 | Common:1; Rare:84 | ||||
| chr17:8138855-8139136 | Common:6; Rare:132 | ||||
| chr17:8154261-8154375 | Rare:20 | ||||
| chr17:8164204-8164604 | Common:2; Rare:111 | ||||
| chr17:8173221-8173916 | Common:26; Rare:543; Clinvar:3; Clinvar (pathogenic):4 | ||||
| chr17:8185615-8186146 | Common:5; Rare:135 | ||||
| chr17:8186719-8186982 | Common:3; Rare:153 | ||||
| chr17:8192238-8192442 | Common:3; Rare:32 |