| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48780245-48780572 | Common:2; Rare:97 | ||||
| chr4:52659268-52659441 | Common:1; Rare:56 | ||||
| chr4:53365980-53366211 | Rare:53 | ||||
| chr4:53377425-53377710 | Common:3; Rare:84 | ||||
| chr4:54657840-54657963 | Rare:40 | ||||
| chr4:55346169-55346333 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395852-55395972 | Common:1; Rare:32; Clinvar:2 | ||||
| chr4:56387428-56387568 | Rare:50 | ||||
| chr4:56435483-56435774 | Common:5; Rare:104 | ||||
| chr4:56435977-56436326 | Rare:121 | ||||
| chr4:56467542-56467694 | Common:2; Rare:64; Clinvar (benign):5 | ||||
| chr4:56821504-56821545 | Rare:9 | ||||
| chr4:56907622-56907953 | Common:3; Rare:116 | ||||
| chr4:56977537-56977746 | Common:2; Rare:79 | ||||
| chr4:57009147-57009402 | Common:2; Rare:47 |