| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55546500-55546707 | Common:3; Rare:41 | ||||
| chr4:55546801-55547012 | Common:2; Rare:73 | ||||
| chr4:55853483-55853814 | Rare:96 | ||||
| chr4:56387149-56387239 | Rare:21 | ||||
| chr4:56387399-56387545 | Rare:53 | ||||
| chr4:56435457-56436315 | Common:6; Rare:292 | ||||
| chr4:56467481-56467703 | Common:2; Rare:93; Clinvar (benign):5 | ||||
| chr4:56530448-56530613 | Common:3; Rare:40 | ||||
| chr4:56907791-56907966 | Common:2; Rare:72 | ||||
| chr4:56977559-56977771 | Common:2; Rare:81 | ||||
| chr4:64409116-64409631 | Common:2; Rare:150 | ||||
| chr4:67545377-67545751 | Common:2; Rare:91 | ||||
| chr4:67701115-67701404 | Common:4; Rare:135 | ||||
| chr4:68349940-68350228 | Common:2; Rare:101 | ||||
| chr4:70688451-70688639 | Common:2; Rare:55 |