| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139301217-139301779 | Common:5; Rare:166 | ||||
| chr4:139453683-139453749 | Common:2; Rare:21 | ||||
| chr4:139453770-139454210 | Common:3; Rare:117; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556103-139556611 | Rare:105 | ||||
| chr4:139556719-139557117 | Common:2; Rare:82 | ||||
| chr4:140373352-140373709 | Common:3; Rare:142 | ||||
| chr4:140524367-140524492 | Common:1; Rare:39 | ||||
| chr4:140756148-140756478 | Common:1; Rare:67 | ||||
| chr4:141132522-141132902 | Common:2; Rare:132 | ||||
| chr4:141636750-141637103 | Common:1; Rare:81 | ||||
| chr4:142405264-142405562 | Common:1; Rare:63 | ||||
| chr4:142846258-142846383 | Rare:25 | ||||
| chr4:142846462-142846623 | Common:1; Rare:32 | ||||
| chr4:143184639-143185161 | Common:9; Rare:197 | ||||
| chr4:143336656-143336912 | Rare:57 |