| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:54229025-54229388 | Common:1; Rare:73; Clinvar (benign):4 | ||||
| chr4:55346159-55346337 | Common:3; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55546567-55546746 | Common:4; Rare:33 | ||||
| chr4:55546805-55547028 | Common:2; Rare:79 | ||||
| chr4:55853469-55853812 | Rare:98 | ||||
| chr4:55948732-55948980 | Common:2; Rare:50 | ||||
| chr4:56048968-56049286 | Common:1; Rare:91 | ||||
| chr4:56387417-56387553 | Rare:44 | ||||
| chr4:56435467-56435973 | Common:6; Rare:166 | ||||
| chr4:56435975-56436315 | Rare:119 | ||||
| chr4:56467482-56467694 | Common:2; Rare:90; Clinvar (benign):5 | ||||
| chr4:56977581-56977785 | Common:1; Rare:75 | ||||
| chr4:61202341-61202638 | Common:1; Rare:64 | ||||
| chr4:65669483-65669592 | Common:1; Rare:27 | ||||
| chr4:65670408-65670646 | Common:1; Rare:58 |