| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6996764-6996903 | Rare:43 | ||||
| chr17:7012315-7012758 | Rare:146 | ||||
| chr17:7035817-7036026 | Rare:51 | ||||
| chr17:7043860-7044118 | Common:3; Rare:54 | ||||
| chr17:7114800-7115083 | Common:2; Rare:59 | ||||
| chr17:7219793-7219971 | Common:3; Rare:83; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7221443-7221618 | Common:4; Rare:64; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:7221728-7222011 | Common:3; Rare:70; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr17:7223630-7223872 | Rare:66; Clinvar:12; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
| chr17:7223942-7224345 | Rare:139; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):13 | ||||
| chr17:7224366-7224714 | Common:4; Rare:128; Clinvar:10; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr17:7241789-7241954 | Common:2; Rare:37 | ||||
| chr17:7242171-7242473 | Common:2; Rare:98 | ||||
| chr17:7251940-7252319 | Common:2; Rare:152 | ||||
| chr17:7261100-7261234 | Common:1; Rare:35 |