| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88284517-88284699 | Rare:34 | ||||
| chr4:88456771-88457138 | Common:4; Rare:91 | ||||
| chr4:88523698-88523877 | Common:2; Rare:59 | ||||
| chr4:88592325-88592497 | Rare:50 | ||||
| chr4:88823214-88823388 | Common:1; Rare:32 | ||||
| chr4:89111303-89111637 | Common:4; Rare:121 | ||||
| chr4:89837043-89837516 | Common:5; Rare:151; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:98261153-98261472 | Common:1; Rare:102 | ||||
| chr4:98929108-98929344 | Common:3; Rare:59 | ||||
| chr4:99088698-99088916 | Common:7; Rare:100 | ||||
| chr4:99564011-99564166 | Common:2; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99946573-99946759 | Rare:66 | ||||
| chr4:99950269-99950533 | Rare:56 | ||||
| chr4:101347417-101347807 | Common:5; Rare:115 | ||||
| chr4:102826784-102827192 | Common:4; Rare:140 |