| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51842804-51843212 | Common:1; Rare:119 | ||||
| chr4:51843345-51843695 | Rare:101 | ||||
| chr4:52038240-52038358 | Rare:48; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52051294-52051441 | Rare:35 | ||||
| chr4:52659183-52659439 | Common:1; Rare:86 | ||||
| chr4:52862150-52862329 | Common:7; Rare:80 | ||||
| chr4:53365963-53366211 | Rare:57 | ||||
| chr4:54064417-54064474 | Rare:13 | ||||
| chr4:55125433-55125762 | Common:3; Rare:86 | ||||
| chr4:55395828-55395968 | Common:2; Rare:35; Clinvar:2 | ||||
| chr4:55396034-55396201 | Common:1; Rare:57 | ||||
| chr4:55546786-55547232 | Common:4; Rare:168 | ||||
| chr4:55853481-55853794 | Rare:88 | ||||
| chr4:56387417-56387543 | Rare:41 | ||||
| chr4:56435458-56435973 | Common:6; Rare:169 |