| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88523591-88523893 | Common:3; Rare:98 | ||||
| chr4:88592202-88592491 | Common:1; Rare:76 | ||||
| chr4:88697760-88697922 | Common:2; Rare:56 | ||||
| chr4:88823222-88823399 | Common:1; Rare:35 | ||||
| chr4:89057115-89057273 | Common:1; Rare:33 | ||||
| chr4:89836902-89837263 | Common:3; Rare:116; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:89837469-89837615 | Rare:27 | ||||
| chr4:89838273-89838360 | Rare:18 | ||||
| chr4:90127288-90127599 | Common:1; Rare:103 | ||||
| chr4:94207576-94208017 | Common:2; Rare:129 | ||||
| chr4:94451727-94451995 | Common:3; Rare:89 | ||||
| chr4:94757754-94758054 | Common:4; Rare:79 | ||||
| chr4:95548777-95549373 | Common:3; Rare:165 | ||||
| chr4:98143450-98143650 | Common:1; Rare:51 | ||||
| chr4:98261136-98261546 | Common:1; Rare:140 |