| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655223-15655466 | Common:2; Rare:97 | ||||
| chr4:15681369-15681884 | Common:4; Rare:173 | ||||
| chr4:15702954-15703134 | Common:2; Rare:36 | ||||
| chr4:17577316-17577561 | Rare:117 | ||||
| chr4:17614522-17614685 | Common:2; Rare:80 | ||||
| chr4:17810652-17811170 | Common:5; Rare:159 | ||||
| chr4:20700302-20700506 | Common:1; Rare:91 | ||||
| chr4:24584365-24584725 | Common:1; Rare:110 | ||||
| chr4:25160347-25160736 | Common:3; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233835-25234081 | Rare:102 | ||||
| chr4:25312600-25312861 | Common:2; Rare:93 | ||||
| chr4:25376984-25377349 | Common:3; Rare:111 | ||||
| chr4:25861575-25861762 | Common:3; Rare:27 | ||||
| chr4:25914051-25914328 | Common:2; Rare:118 | ||||
| chr4:26319363-26319760 | Rare:109 |