| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102501980-102502348 | Common:3; Rare:116 | ||||
| chr10:102502641-102503016 | Common:1; Rare:107 | ||||
| chr10:102503689-102504046 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:102643364-102644182 | Common:1; Rare:215 | ||||
| chr10:102644184-102644545 | Common:1; Rare:101 | ||||
| chr10:102644622-102644907 | Rare:64 | ||||
| chr10:102644913-102645241 | Rare:81 | ||||
| chr10:102645384-102646309 | Common:4; Rare:201 | ||||
| chr10:102713862-102714055 | Rare:34 | ||||
| chr10:102714261-102714916 | Common:4; Rare:177 | ||||
| chr10:102715007-102715067 | Common:1; Rare:9 | ||||
| chr10:102743737-102744037 | Common:2; Rare:74 | ||||
| chr10:102854171-102854330 | Common:1; Rare:63 | ||||
| chr10:102854347-102854663 | Common:1; Rare:87 | ||||
| chr10:102917929-102918618 | Common:3; Rare:267; Clinvar:1; Clinvar (benign):2 |