| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41990402-41990579 | Common:1; Rare:64 | ||||
| chr4:44678315-44678706 | Common:2; Rare:144 | ||||
| chr4:44726547-44726629 | Rare:35 | ||||
| chr4:47485187-47485408 | Common:2; Rare:71 | ||||
| chr4:48016634-48016784 | Common:1; Rare:44 | ||||
| chr4:48341191-48341552 | Common:2; Rare:148 | ||||
| chr4:48780175-48780568 | Common:3; Rare:122 | ||||
| chr4:52038230-52038323 | Rare:43; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr4:52659181-52659462 | Common:1; Rare:93 | ||||
| chr4:54064490-54064973 | Common:5; Rare:139 | ||||
| chr4:55346197-55346337 | Common:3; Rare:49; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395818-55395968 | Common:2; Rare:37; Clinvar:2 | ||||
| chr4:55546808-55547012 | Common:2; Rare:69 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435546-56435778 | Common:3; Rare:77 |