| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102450334-102450804 | Common:1; Rare:191 | ||||
| chr10:102632614-102632844 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:102641987-102642576 | Common:3; Rare:152 | ||||
| chr10:102643369-102643778 | Common:1; Rare:99 | ||||
| chr10:102645793-102646431 | Common:3; Rare:138 | ||||
| chr10:102647759-102647910 | Rare:30 | ||||
| chr10:102652132-102652566 | Common:6; Rare:66 | ||||
| chr10:102675187-102675272 | Rare:17 | ||||
| chr10:102712336-102712367 | Rare:3 | ||||
| chr10:102796447-102796600 | Rare:33 | ||||
| chr10:102803242-102803381 | Rare:31 | ||||
| chr10:103053967-103054118 | Rare:32 | ||||
| chr10:103069419-103069581 | Common:1; Rare:39 | ||||
| chr10:103070426-103070450 | Common:1; Rare:6 | ||||
| chr10:103112683-103112815 | Common:2; Rare:22 |