| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55546567-55546735 | Common:4; Rare:29 | ||||
| chr4:55546805-55547028 | Common:2; Rare:79 | ||||
| chr4:55547124-55547185 | Rare:20 | ||||
| chr4:55853448-55853795 | Rare:97 | ||||
| chr4:56387399-56387569 | Rare:62 | ||||
| chr4:56435467-56435791 | Common:5; Rare:111 | ||||
| chr4:56435947-56436321 | Rare:139 | ||||
| chr4:56467437-56467694 | Common:2; Rare:98; Clinvar (benign):5 | ||||
| chr4:56681013-56681435 | Common:1; Rare:71 | ||||
| chr4:56681624-56682026 | Common:3; Rare:59 | ||||
| chr4:56977581-56977777 | Common:1; Rare:72 | ||||
| chr4:65669478-65669645 | Common:1; Rare:45 | ||||
| chr4:65670357-65670646 | Common:1; Rare:74 | ||||
| chr4:65670683-65670916 | Common:2; Rare:49 | ||||
| chr4:67545363-67545748 | Common:2; Rare:94 |