| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48269790-48269985 | Common:2; Rare:43 | ||||
| chr4:48780193-48780626 | Common:3; Rare:134 | ||||
| chr4:52038240-52038359 | Rare:48; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659180-52659439 | Common:1; Rare:87 | ||||
| chr4:52862152-52862322 | Common:7; Rare:76 | ||||
| chr4:53377612-53377751 | Common:2; Rare:56 | ||||
| chr4:53591577-53591865 | Common:2; Rare:59 | ||||
| chr4:55395817-55395957 | Common:2; Rare:37; Clinvar:2 | ||||
| chr4:55546816-55547011 | Common:2; Rare:68 | ||||
| chr4:55853464-55853789 | Rare:89 | ||||
| chr4:56387423-56387553 | Rare:44 | ||||
| chr4:56435473-56436315 | Common:6; Rare:287 | ||||
| chr4:56467515-56467704 | Common:2; Rare:79; Clinvar (benign):5 | ||||
| chr4:56656404-56656765 | Common:5; Rare:62 | ||||
| chr4:56977574-56977785 | Common:1; Rare:81 |