| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:128809595-128809823 | Rare:69 | ||||
| chr4:139301231-139301549 | Common:4; Rare:90 | ||||
| chr4:140373357-140373720 | Common:3; Rare:142 | ||||
| chr4:140756328-140756433 | Rare:23 | ||||
| chr4:143184851-143184985 | Common:5; Rare:51 | ||||
| chr4:144645874-144646288 | Common:3; Rare:111 | ||||
| chr4:145098146-145098404 | Rare:86 | ||||
| chr4:145619302-145619406 | Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:151226361-151226515 | Rare:27 | ||||
| chr4:151760940-151761216 | Rare:110 | ||||
| chr4:152679943-152680144 | Rare:44 | ||||
| chr4:152779634-152780016 | Common:2; Rare:99 | ||||
| chr4:158172639-158172854 | Common:1; Rare:35 | ||||
| chr4:158671825-158672325 | Common:5; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:169010226-169010371 | Common:1; Rare:50 |