| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15702804-15703117 | Common:2; Rare:59 | ||||
| chr4:17577316-17577552 | Rare:111 | ||||
| chr4:17614544-17614651 | Common:2; Rare:46 | ||||
| chr4:17810681-17811080 | Common:4; Rare:124 | ||||
| chr4:20700293-20700480 | Rare:84 | ||||
| chr4:25160411-25160725 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233843-25234058 | Rare:92 | ||||
| chr4:25377002-25377295 | Common:3; Rare:90 | ||||
| chr4:25914051-25914328 | Common:2; Rare:118 | ||||
| chr4:26320453-26320832 | Common:1; Rare:120 | ||||
| chr4:26320898-26321046 | Rare:53; Clinvar (benign):1 | ||||
| chr4:26583981-26584129 | Rare:30 | ||||
| chr4:30720012-30720083 | Rare:14 | ||||
| chr4:30720281-30720617 | Common:2; Rare:88 | ||||
| chr4:37826418-37826744 | Common:8; Rare:109 |