| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:140153052-140153120 | Rare:16 | ||||
| chr4:140373331-140373736 | Common:3; Rare:157 | ||||
| chr4:140756327-140756433 | Rare:23 | ||||
| chr4:141636785-141637074 | Common:1; Rare:59 | ||||
| chr4:143184650-143184960 | Common:8; Rare:122 | ||||
| chr4:143337080-143337198 | Rare:47 | ||||
| chr4:143513624-143514098 | Common:2; Rare:187 | ||||
| chr4:144645910-144646178 | Common:1; Rare:72 | ||||
| chr4:144646492-144646938 | Rare:126 | ||||
| chr4:145098129-145098411 | Rare:87 | ||||
| chr4:145150668-145150875 | Rare:63 | ||||
| chr4:145179580-145179810 | Rare:81 | ||||
| chr4:145619296-145619410 | Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:145938374-145938530 | Rare:33 | ||||
| chr4:145938724-145938968 | Rare:55 |