| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73505341-73505539 | Common:1; Rare:44 | ||||
| chr10:73625947-73626106 | Rare:29 | ||||
| chr10:73743996-73744143 | Rare:37 | ||||
| chr10:73744220-73744437 | Common:1; Rare:60 | ||||
| chr10:73772072-73772325 | Common:3; Rare:77 | ||||
| chr10:73772420-73772716 | Rare:141 | ||||
| chr10:73781969-73782084 | Common:1; Rare:36 | ||||
| chr10:73874448-73874735 | Rare:74 | ||||
| chr10:73997941-73998303 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:74104969-74105162 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:74151061-74151275 | Common:1; Rare:66 | ||||
| chr10:74176609-74176849 | Rare:66; Clinvar:3 | ||||
| chr10:74825262-74825606 | Rare:88 | ||||
| chr10:74826391-74826636 | Rare:58; Clinvar (benign):2 | ||||
| chr10:75210487-75210873 | Common:1; Rare:130 |