| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801263-121801401 | Common:2; Rare:44 | ||||
| chr4:127880759-127880932 | Rare:64 | ||||
| chr4:128061002-128061325 | Common:1; Rare:116 | ||||
| chr4:129093483-129093731 | Common:1; Rare:76 | ||||
| chr4:139301422-139301538 | Common:1; Rare:34 | ||||
| chr4:140373380-140373662 | Common:2; Rare:101 | ||||
| chr4:142405389-142405518 | Rare:22 | ||||
| chr4:145098156-145098337 | Rare:65 | ||||
| chr4:152679955-152680112 | Rare:26 | ||||
| chr4:152779762-152780005 | Common:1; Rare:64 | ||||
| chr4:158671868-158672313 | Common:5; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:169010268-169010435 | Common:1; Rare:51 | ||||
| chr4:173334245-173334757 | Rare:132 | ||||
| chr4:177442376-177442554 | Rare:105; Clinvar:2 | ||||
| chr4:183659132-183659323 | Common:1; Rare:56 |