| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48831653-48831664 | Rare:3 | ||||
| chr4:51844668-51844925 | Common:1; Rare:71 | ||||
| chr4:52038246-52038321 | Rare:31; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52659180-52659420 | Common:1; Rare:82 | ||||
| chr4:53365949-53366222 | Rare:60 | ||||
| chr4:53377547-53377830 | Common:2; Rare:101 | ||||
| chr4:53377869-53377912 | Rare:10 | ||||
| chr4:55125575-55125705 | Common:2; Rare:27 | ||||
| chr4:55346159-55346343 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395846-55395959 | Common:1; Rare:31; Clinvar:2 | ||||
| chr4:55546589-55546735 | Common:4; Rare:26 | ||||
| chr4:55546795-55547003 | Common:2; Rare:72 | ||||
| chr4:55948708-55948976 | Common:1; Rare:54 | ||||
| chr4:56387149-56387230 | Rare:19 | ||||
| chr4:56387409-56387553 | Rare:48 |