| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25233837-25234156 | Rare:230 | ||||
| chr4:25312555-25312873 | Common:2; Rare:117 | ||||
| chr4:25376948-25377366 | Common:7; Rare:242 | ||||
| chr4:25914038-25914325 | Common:4; Rare:225 | ||||
| chr4:26319360-26319838 | Rare:194 | ||||
| chr4:26320480-26320850 | Common:2; Rare:205 | ||||
| chr4:26320874-26321067 | Rare:113; Clinvar (benign):1 | ||||
| chr4:26583941-26584139 | Rare:70 | ||||
| chr4:26857484-26857776 | Common:8; Rare:156 | ||||
| chr4:26860568-26860856 | Common:6; Rare:196 | ||||
| chr4:37686298-37686581 | Common:4; Rare:179 | ||||
| chr4:37826486-37826750 | Common:13; Rare:161 | ||||
| chr4:37977133-37977447 | Rare:137 | ||||
| chr4:38109960-38110310 | Common:1; Rare:84 | ||||
| chr4:38132920-38133590 | Common:1; Rare:267; Clinvar:2 |