| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99563989-99564123 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr4:99816558-99816866 | Common:1; Rare:45 | ||||
| chr4:99894357-99894608 | Common:2; Rare:89 | ||||
| chr4:99946557-99946759 | Rare:71 | ||||
| chr4:99950242-99950499 | Rare:53 | ||||
| chr4:101347528-101347816 | Common:5; Rare:90 | ||||
| chr4:102760911-102761052 | Rare:47; Clinvar:1 | ||||
| chr4:102825778-102825891 | Rare:25 | ||||
| chr4:102826837-102826968 | Rare:39 | ||||
| chr4:102827148-102827427 | Common:1; Rare:96 | ||||
| chr4:102827458-102827895 | Common:4; Rare:146 | ||||
| chr4:102827911-102828288 | Common:3; Rare:129 | ||||
| chr4:102868850-102869068 | Common:2; Rare:77 | ||||
| chr4:103076303-103076372 | Rare:22 | ||||
| chr4:104494886-104495198 | Common:3; Rare:64 |