| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48780226-48780634 | Common:4; Rare:123 | ||||
| chr4:48830834-48831151 | Common:1; Rare:107 | ||||
| chr4:51842823-51843216 | Common:1; Rare:117 | ||||
| chr4:52038248-52038327 | Rare:31; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52659188-52659420 | Common:1; Rare:80 | ||||
| chr4:52862152-52862322 | Common:7; Rare:76 | ||||
| chr4:53365997-53366105 | Rare:21 | ||||
| chr4:53377425-53377710 | Common:3; Rare:84 | ||||
| chr4:54064493-54064823 | Common:5; Rare:106 | ||||
| chr4:55546586-55546726 | Common:4; Rare:27 | ||||
| chr4:55546816-55547028 | Common:2; Rare:77 | ||||
| chr4:56387357-56387553 | Rare:62 | ||||
| chr4:56435458-56435974 | Common:6; Rare:170 | ||||
| chr4:56435987-56436327 | Rare:119 | ||||
| chr4:56436411-56436459 | Rare:10 |