| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147684106-147684247 | Common:1; Rare:54 | ||||
| chr4:151015267-151015364 | Rare:25 | ||||
| chr4:152779855-152780013 | Common:1; Rare:41 | ||||
| chr4:153344562-153344730 | Common:4; Rare:48 | ||||
| chr4:154550372-154550512 | Rare:43 | ||||
| chr4:158671825-158672321 | Common:5; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723331-158723463 | Common:2; Rare:59 | ||||
| chr4:159229228-159229411 | Common:1; Rare:28 | ||||
| chr4:165327418-165327728 | Common:2; Rare:88 | ||||
| chr4:168480452-168480500 | Common:1; Rare:13 | ||||
| chr4:169010227-169010430 | Common:1; Rare:64 | ||||
| chr4:173333498-173333883 | Common:2; Rare:99 | ||||
| chr4:173334308-173334649 | Rare:92 | ||||
| chr4:173370690-173370961 | Common:2; Rare:67 | ||||
| chr4:174283612-174284005 | Common:1; Rare:82 |