| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7483915-7484012 | Common:2; Rare:24 | ||||
| chr17:7484207-7484371 | Common:1; Rare:67 | ||||
| chr17:7484649-7484693 | Common:1; Rare:23 | ||||
| chr17:7484697-7484844 | Rare:58 | ||||
| chr17:7497810-7498175 | Common:3; Rare:135 | ||||
| chr17:7548970-7549294 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558222-7558325 | Rare:27 | ||||
| chr17:7561792-7561999 | Common:2; Rare:54 | ||||
| chr17:7577444-7577704 | Rare:73 | ||||
| chr17:7579440-7579925 | Common:2; Rare:172 | ||||
| chr17:7580201-7580585 | Common:1; Rare:114 | ||||
| chr17:7580735-7580827 | Common:1; Rare:32 | ||||
| chr17:7583706-7583872 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584073-7584098 | Rare:4 | ||||
| chr17:7626760-7627061 | Common:2; Rare:78 |