| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51843340-51843570 | Rare:75 | ||||
| chr4:52038243-52038339 | Rare:40; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659177-52659420 | Common:1; Rare:84 | ||||
| chr4:53591413-53591636 | Common:2; Rare:43 | ||||
| chr4:54064543-54064841 | Common:5; Rare:105 | ||||
| chr4:54228937-54229409 | Common:1; Rare:94; Clinvar (benign):4 | ||||
| chr4:54657815-54658037 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:55125346-55125422 | Rare:22 | ||||
| chr4:55346204-55346347 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395845-55395979 | Common:1; Rare:37; Clinvar:2 | ||||
| chr4:55396050-55396214 | Common:1; Rare:58; Clinvar (benign):2 | ||||
| chr4:55546494-55547026 | Common:6; Rare:156 | ||||
| chr4:55547102-55547237 | Common:2; Rare:54 | ||||
| chr4:55948742-55948956 | Common:1; Rare:41 | ||||
| chr4:56387423-56387528 | Rare:35 |