| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143337085-143337206 | Rare:48 | ||||
| chr4:143513296-143513541 | Common:3; Rare:93 | ||||
| chr4:143513650-143514027 | Common:1; Rare:150 | ||||
| chr4:143905551-143905833 | Common:1; Rare:61 | ||||
| chr4:144645826-144646178 | Common:1; Rare:105 | ||||
| chr4:144646458-144646697 | Common:1; Rare:61 | ||||
| chr4:145098134-145098364 | Rare:78 | ||||
| chr4:145482869-145483002 | Rare:21 | ||||
| chr4:145619328-145619416 | Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:145938858-145939016 | Rare:48 | ||||
| chr4:146521859-146521965 | Rare:22 | ||||
| chr4:147617254-147617446 | Common:1; Rare:41 | ||||
| chr4:147684096-147684302 | Common:1; Rare:85 | ||||
| chr4:148442368-148442712 | Rare:100; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581723-150582111 | Common:1; Rare:75 |