| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141636828-141637001 | Rare:35 | ||||
| chr4:143184657-143185162 | Common:8; Rare:189 | ||||
| chr4:144645832-144646168 | Common:1; Rare:100 | ||||
| chr4:145098134-145098359 | Rare:76 | ||||
| chr4:145619313-145619402 | Rare:38 | ||||
| chr4:147617223-147617479 | Common:1; Rare:58 | ||||
| chr4:147684096-147684292 | Common:1; Rare:77 | ||||
| chr4:148442350-148442712 | Rare:104; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015220-151015350 | Rare:39 | ||||
| chr4:151015707-151015833 | Rare:56 | ||||
| chr4:151099493-151099713 | Common:3; Rare:89 | ||||
| chr4:151408910-151409188 | Common:4; Rare:93 | ||||
| chr4:152536053-152536407 | Common:2; Rare:136 | ||||
| chr4:152779730-152780172 | Common:2; Rare:113 | ||||
| chr4:154550346-154550550 | Common:1; Rare:70 |