| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139302460-139302564 | Common:1; Rare:16 | ||||
| chr4:139453686-139453696 | Rare:4 | ||||
| chr4:139453697-139454210 | Common:4; Rare:142; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556181-139556513 | Rare:64 | ||||
| chr4:139557125-139557291 | Common:2; Rare:29 | ||||
| chr4:140373374-140373701 | Common:2; Rare:131 | ||||
| chr4:140756110-140756439 | Common:1; Rare:66 | ||||
| chr4:141220839-141220971 | Rare:44 | ||||
| chr4:143184859-143184998 | Common:3; Rare:54 | ||||
| chr4:143336520-143336851 | Rare:69 | ||||
| chr4:143513817-143514027 | Common:1; Rare:91 | ||||
| chr4:145098148-145098363 | Rare:75 | ||||
| chr4:145180557-145180836 | Common:1; Rare:77 | ||||
| chr4:145482826-145483001 | Rare:29 | ||||
| chr4:145619320-145619402 | Rare:32 |