| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93921641-93921869 | Common:3; Rare:45 | ||||
| chr7:94394678-94394924 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr7:94425779-94426050 | Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:94656105-94656391 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:97117459-97117752 | Common:2; Rare:125 | ||||
| chr7:97872354-97872547 | Rare:68 | ||||
| chr7:98252216-98252348 | Rare:28 | ||||
| chr7:99325808-99325983 | Common:1; Rare:66 | ||||
| chr7:99408537-99408706 | Common:2; Rare:51 | ||||
| chr7:99408811-99409037 | Common:1; Rare:71 | ||||
| chr7:99438731-99438985 | Common:1; Rare:78 | ||||
| chr7:99472646-99472912 | Common:4; Rare:83 | ||||
| chr7:99500284-99500437 | Common:1; Rare:38 | ||||
| chr7:99552075-99552197 | Rare:42 | ||||
| chr7:99558519-99558720 | Common:2; Rare:66 |