| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112644475-112644844 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:112646214-112646451 | Rare:81; Clinvar:1 | ||||
| chr4:112646685-112646696 | Rare:5 | ||||
| chr4:112646743-112646827 | Rare:31 | ||||
| chr4:112647497-112647833 | Common:4; Rare:125 | ||||
| chr4:113145542-113145755 | Rare:37 | ||||
| chr4:113292803-113293012 | Common:2; Rare:42 | ||||
| chr4:113761742-113761916 | Common:1; Rare:36 | ||||
| chr4:113979131-113979174 | Rare:6 | ||||
| chr4:114598328-114598455 | Common:1; Rare:34 | ||||
| chr4:114598645-114598921 | Common:9; Rare:77 | ||||
| chr4:114598946-114599201 | Common:2; Rare:35 | ||||
| chr4:118685271-118685478 | Common:3; Rare:68 | ||||
| chr4:118835704-118835796 | Common:1; Rare:15 | ||||
| chr4:118836056-118836232 | Common:1; Rare:40 |