| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124403550-124403810 | Common:1; Rare:74 | ||||
| chr10:124418911-124419256 | Common:6; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:124450038-124450273 | Common:5; Rare:64 | ||||
| chr10:124461650-124461914 | Common:5; Rare:82 | ||||
| chr10:124462020-124462336 | Common:4; Rare:97 | ||||
| chr10:124743980-124744900 | Common:2; Rare:274 | ||||
| chr10:124791699-124792012 | Common:3; Rare:153 | ||||
| chr10:124792171-124792431 | Common:1; Rare:51 | ||||
| chr10:124801664-124801884 | Rare:66 | ||||
| chr10:125158715-125158932 | Rare:61 | ||||
| chr10:125159097-125159497 | Common:4; Rare:227 | ||||
| chr10:125159466-125160044 | Common:3; Rare:185 | ||||
| chr10:125160521-125160954 | Common:1; Rare:79 | ||||
| chr10:125161340-125161770 | Common:1; Rare:117 | ||||
| chr10:125719417-125719752 | Common:1; Rare:123 |