| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143336270-143336527 | Rare:90 | ||||
| chr4:143336613-143337013 | Common:1; Rare:149 | ||||
| chr4:143337085-143337201 | Rare:47 | ||||
| chr4:143513345-143513759 | Common:4; Rare:211 | ||||
| chr4:145098137-145098372 | Rare:158 | ||||
| chr4:145179630-145180060 | Rare:265 | ||||
| chr4:145180396-145180762 | Common:2; Rare:196 | ||||
| chr4:145481378-145481917 | Common:12; Rare:182 | ||||
| chr4:145482510-145483190 | Common:1; Rare:245 | ||||
| chr4:145619298-145619445 | Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:146521810-146522019 | Rare:72 | ||||
| chr4:146522220-146522550 | Common:8; Rare:132 | ||||
| chr4:147617225-147617507 | Common:2; Rare:122 | ||||
| chr4:147684058-147684298 | Common:2; Rare:151 | ||||
| chr4:147731844-147732156 | Common:2; Rare:186 |