| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143337103-143337211 | Rare:45 | ||||
| chr4:143513325-143514027 | Common:4; Rare:257 | ||||
| chr4:144140673-144140729 | Rare:13 | ||||
| chr4:144645805-144646187 | Common:1; Rare:111 | ||||
| chr4:144646540-144646697 | Rare:45 | ||||
| chr4:145098134-145098361 | Rare:77 | ||||
| chr4:145481683-145481720 | Rare:9 | ||||
| chr4:145482869-145483029 | Rare:31 | ||||
| chr4:145619181-145619402 | Rare:80 | ||||
| chr4:146521867-146521995 | Rare:32 | ||||
| chr4:147617217-147617479 | Common:1; Rare:60 | ||||
| chr4:147684081-147684316 | Common:1; Rare:97 | ||||
| chr4:148442375-148442712 | Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:150079037-150079364 | Common:2; Rare:115 | ||||
| chr4:150581695-150581976 | Common:1; Rare:57 |