| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7455533-7455831 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7479508-7479750 | Common:1; Rare:42 | ||||
| chr17:7483926-7484022 | Common:2; Rare:23 | ||||
| chr17:7484222-7484387 | Common:1; Rare:72 | ||||
| chr17:7484697-7484852 | Rare:61 | ||||
| chr17:7573238-7573531 | Common:4; Rare:99 | ||||
| chr17:7583535-7583877 | Common:1; Rare:138; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584074-7584182 | Rare:25 | ||||
| chr17:7590080-7590163 | Rare:17 | ||||
| chr17:7687457-7687608 | Rare:34; Clinvar:1 | ||||
| chr17:7843634-7843735 | Rare:38 | ||||
| chr17:7857163-7857432 | Common:2; Rare:134 | ||||
| chr17:7857467-7857756 | Common:2; Rare:94 | ||||
| chr17:7857915-7858080 | Rare:59 | ||||
| chr17:7885517-7885662 | Rare:31 |