| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100286623-100286722 | Common:2; Rare:62 | ||||
| chr10:100346917-100347543 | Common:5; Rare:148 | ||||
| chr10:100912751-100912996 | Common:1; Rare:76 | ||||
| chr10:100913335-100913371 | Rare:13 | ||||
| chr10:100987440-100987571 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996749-100997109 | Common:1; Rare:81 | ||||
| chr10:101031132-101031533 | Rare:91 | ||||
| chr10:101588166-101588362 | Rare:82; Clinvar:1 | ||||
| chr10:101818340-101818762 | Common:1; Rare:114 | ||||
| chr10:101843830-101844131 | Common:3; Rare:98 | ||||
| chr10:102056089-102056373 | Common:1; Rare:69 | ||||
| chr10:102394336-102394531 | Rare:54 | ||||
| chr10:102395558-102395730 | Common:1; Rare:48 | ||||
| chr10:102432546-102432835 | Common:2; Rare:86 | ||||
| chr10:102644804-102645147 | Rare:83 |