| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77028338-77028683 | Common:3; Rare:62 | ||||
| chr4:77056249-77056436 | Common:3; Rare:47 | ||||
| chr4:77075476-77075529 | Rare:22 | ||||
| chr4:77075544-77075582 | Rare:15 | ||||
| chr4:77075753-77076114 | Common:7; Rare:148 | ||||
| chr4:77819348-77819639 | Common:1; Rare:81 | ||||
| chr4:77862643-77862872 | Common:3; Rare:84 | ||||
| chr4:78551557-78551850 | Rare:71 | ||||
| chr4:78551983-78552174 | Common:2; Rare:49 | ||||
| chr4:78554346-78554487 | Common:1; Rare:32 | ||||
| chr4:78939186-78939567 | Common:2; Rare:163 | ||||
| chr4:80072158-80072312 | Common:2; Rare:36 | ||||
| chr4:80072443-80072837 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:80072839-80072892 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr4:80072895-80073276 | Common:2; Rare:112; Clinvar:6; Clinvar (benign):2 |