| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88007533-88007682 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:88284542-88284967 | Common:2; Rare:108 | ||||
| chr4:88456780-88457250 | Common:4; Rare:134 | ||||
| chr4:88523684-88523906 | Common:3; Rare:67 | ||||
| chr4:88592200-88592570 | Common:1; Rare:107 | ||||
| chr4:88593010-88593340 | Common:3; Rare:81 | ||||
| chr4:88697791-88697932 | Common:2; Rare:41 | ||||
| chr4:88823163-88823452 | Common:2; Rare:58 | ||||
| chr4:89057120-89057304 | Common:2; Rare:43 | ||||
| chr4:89111350-89111544 | Common:4; Rare:71 | ||||
| chr4:89307880-89308210 | Common:4; Rare:98 | ||||
| chr4:89836969-89837310 | Common:4; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:89837420-89837593 | Rare:40 | ||||
| chr4:89879305-89879530 | Rare:38 | ||||
| chr4:89879686-89880290 | Common:6; Rare:158 |