| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139301313-139301543 | Common:3; Rare:71 | ||||
| chr4:139453683-139453697 | Common:1; Rare:6 | ||||
| chr4:139453770-139454190 | Common:3; Rare:106; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556109-139556168 | Rare:16 | ||||
| chr4:139556381-139556677 | Common:1; Rare:46 | ||||
| chr4:140373390-140373697 | Common:2; Rare:125 | ||||
| chr4:141636769-141636991 | Common:1; Rare:47 | ||||
| chr4:142405401-142405570 | Common:1; Rare:27 | ||||
| chr4:143184672-143184985 | Common:8; Rare:121 | ||||
| chr4:143513348-143513538 | Common:2; Rare:68 | ||||
| chr4:143513642-143513819 | Rare:61 | ||||
| chr4:145098141-145098341 | Rare:69 | ||||
| chr4:145619350-145619402 | Rare:17 | ||||
| chr4:147480646-147481101 | Common:2; Rare:82 | ||||
| chr4:147684096-147684265 | Common:1; Rare:65 |