| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8176316-8176483 | Rare:53 | ||||
| chr17:8248029-8248182 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249207-8249319 | Common:1; Rare:32 | ||||
| chr17:8295352-8295518 | Common:1; Rare:45 | ||||
| chr17:8376618-8376833 | Common:1; Rare:98 | ||||
| chr17:8965651-8965777 | Common:1; Rare:32 | ||||
| chr17:10019831-10020079 | Common:1; Rare:62 | ||||
| chr17:10697398-10697654 | Common:3; Rare:115; Clinvar:5; Clinvar (benign):6 | ||||
| chr17:10729749-10729816 | Rare:36 | ||||
| chr17:12665809-12666233 | Common:2; Rare:95 | ||||
| chr17:14069349-14069608 | Common:2; Rare:97; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:15260650-15260961 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:15262431-15262645 | Rare:47 | ||||
| chr17:15699506-15699773 | Common:3; Rare:71 | ||||
| chr17:15999600-16000032 | Common:3; Rare:184; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 |