| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15339745-15339799 | Rare:10 | ||||
| chr4:15339830-15340190 | Common:1; Rare:80 | ||||
| chr4:15427912-15428060 | Rare:17 | ||||
| chr4:15655223-15655466 | Common:2; Rare:97 | ||||
| chr4:15681466-15681879 | Common:4; Rare:143 | ||||
| chr4:16898481-16898969 | Common:14; Rare:92 | ||||
| chr4:17577342-17577550 | Rare:102 | ||||
| chr4:17614546-17614664 | Common:2; Rare:52 | ||||
| chr4:17810586-17811086 | Common:4; Rare:148 | ||||
| chr4:23889994-23890231 | Rare:38 | ||||
| chr4:24584463-24584679 | Rare:69 | ||||
| chr4:24795362-24795613 | Common:1; Rare:61 | ||||
| chr4:25160347-25160732 | Common:3; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233837-25234015 | Rare:71 | ||||
| chr4:25914051-25914308 | Common:2; Rare:110 |