| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98657647-98657788 | Rare:32 | ||||
| chr4:98929031-98929366 | Common:3; Rare:99 | ||||
| chr4:98995508-98995774 | Common:5; Rare:91 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563989-99564123 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr4:99894333-99894628 | Common:3; Rare:98 | ||||
| chr4:99946533-99946786 | Rare:97 | ||||
| chr4:99950228-99950533 | Rare:72 | ||||
| chr4:101347483-101347905 | Common:5; Rare:114 | ||||
| chr4:101348030-101348189 | Rare:44 | ||||
| chr4:102345459-102345618 | Rare:40 | ||||
| chr4:102760908-102761049 | Rare:48; Clinvar:1 | ||||
| chr4:102825772-102825891 | Rare:28 | ||||
| chr4:102827115-102827391 | Common:1; Rare:102 | ||||
| chr4:102827442-102828299 | Common:7; Rare:284 |