| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17614551-17614652 | Common:2; Rare:43 | ||||
| chr4:17810681-17811039 | Common:3; Rare:112 | ||||
| chr4:20700322-20700486 | Common:1; Rare:68 | ||||
| chr4:24584463-24584666 | Rare:68 | ||||
| chr4:24795342-24795613 | Common:1; Rare:65 | ||||
| chr4:25160405-25160732 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914028-25914301 | Common:2; Rare:117 | ||||
| chr4:26320635-26320859 | Common:1; Rare:100 | ||||
| chr4:26320900-26321041 | Rare:49; Clinvar (benign):1 | ||||
| chr4:30720237-30720605 | Common:3; Rare:94 | ||||
| chr4:37826534-37826760 | Common:6; Rare:84 | ||||
| chr4:37977143-37977447 | Rare:79 | ||||
| chr4:38867592-38867822 | Common:2; Rare:83 | ||||
| chr4:38868061-38868126 | Rare:20 | ||||
| chr4:39366324-39366397 | Rare:23 |