| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99472639-99472935 | Common:4; Rare:91 | ||||
| chr7:99500232-99500430 | Common:2; Rare:53 | ||||
| chr7:99504629-99505029 | Rare:101 | ||||
| chr7:99505155-99505325 | Common:5; Rare:55 | ||||
| chr7:99551976-99552197 | Rare:70 | ||||
| chr7:99558401-99558903 | Common:5; Rare:145 | ||||
| chr7:99616847-99617000 | Common:2; Rare:51 | ||||
| chr7:99919495-99919667 | Rare:56 | ||||
| chr7:100015470-100015647 | Common:1; Rare:50 | ||||
| chr7:100049750-100049823 | Rare:35 | ||||
| chr7:100081675-100081983 | Common:2; Rare:85 | ||||
| chr7:100088875-100089081 | Common:1; Rare:65 | ||||
| chr7:100100023-100100318 | Common:1; Rare:137 | ||||
| chr7:100101266-100101748 | Common:1; Rare:196; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100119257-100119717 | Common:1; Rare:138 |