| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52038255-52038346 | Rare:35; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:53365972-53366222 | Rare:57 | ||||
| chr4:53377516-53377718 | Common:1; Rare:69 | ||||
| chr4:54064576-54064855 | Common:4; Rare:94 | ||||
| chr4:55853469-55853689 | Rare:50 | ||||
| chr4:55948720-55948964 | Common:1; Rare:49 | ||||
| chr4:56387423-56387553 | Rare:44 | ||||
| chr4:56435422-56435973 | Common:6; Rare:176 | ||||
| chr4:56435994-56436308 | Rare:112 | ||||
| chr4:56467542-56467689 | Common:2; Rare:63; Clinvar (benign):4 | ||||
| chr4:56821678-56821854 | Common:8; Rare:59 | ||||
| chr4:56977581-56977785 | Common:1; Rare:75 | ||||
| chr4:67545364-67545400 | Rare:4 | ||||
| chr4:67545402-67545768 | Common:2; Rare:90 | ||||
| chr4:67701106-67701421 | Common:4; Rare:145 |