| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15681414-15681879 | Common:4; Rare:154 | ||||
| chr4:15702934-15703129 | Common:2; Rare:39 | ||||
| chr4:17614555-17614651 | Common:2; Rare:40 | ||||
| chr4:17810687-17811045 | Common:4; Rare:113 | ||||
| chr4:25160382-25160704 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25376993-25377322 | Common:3; Rare:99 | ||||
| chr4:25914051-25914308 | Common:2; Rare:110 | ||||
| chr4:26320946-26321044 | Rare:41 | ||||
| chr4:37826640-37826744 | Common:1; Rare:44 | ||||
| chr4:38867589-38867826 | Common:2; Rare:84 | ||||
| chr4:39458857-39459120 | Common:3; Rare:152; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527359-39527754 | Common:2; Rare:93 | ||||
| chr4:39638847-39639142 | Common:1; Rare:109 | ||||
| chr4:39697923-39698185 | Common:2; Rare:115 | ||||
| chr4:41261712-41261922 | Rare:78; Clinvar:1 |