| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15681458-15681686 | Rare:71 | ||||
| chr4:15681720-15681879 | Common:2; Rare:60 | ||||
| chr4:16083677-16083868 | Common:2; Rare:57 | ||||
| chr4:16083896-16084125 | Common:2; Rare:57 | ||||
| chr4:16226466-16226672 | Common:3; Rare:82 | ||||
| chr4:16898540-16898804 | Common:1; Rare:35 | ||||
| chr4:17577315-17577550 | Rare:111 | ||||
| chr4:17614547-17614727 | Common:3; Rare:109 | ||||
| chr4:17810501-17811186 | Common:6; Rare:200 | ||||
| chr4:22515923-22516152 | Common:4; Rare:80 | ||||
| chr4:24584239-24584737 | Common:1; Rare:158 | ||||
| chr4:24795483-24795637 | Common:1; Rare:24 | ||||
| chr4:24912972-24913252 | Common:4; Rare:82 | ||||
| chr4:25160370-25160705 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233820-25234070 | Rare:99 |