| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143337085-143337191 | Rare:43 | ||||
| chr4:143513349-143513779 | Common:2; Rare:142 | ||||
| chr4:144645877-144646168 | Common:1; Rare:83 | ||||
| chr4:144646596-144646697 | Rare:33 | ||||
| chr4:145098134-145098379 | Rare:81 | ||||
| chr4:145180563-145180919 | Common:1; Rare:97 | ||||
| chr4:145481644-145481703 | Rare:14 | ||||
| chr4:145619313-145619427 | Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145938786-145938995 | Rare:54 | ||||
| chr4:145938997-145939075 | Common:1; Rare:22 | ||||
| chr4:146175621-146175806 | Common:1; Rare:61 | ||||
| chr4:146522327-146522468 | Common:3; Rare:55 | ||||
| chr4:147617185-147617470 | Common:1; Rare:67 | ||||
| chr4:147684096-147684336 | Common:1; Rare:100 | ||||
| chr4:147731967-147732319 | Common:1; Rare:129 |