| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89837048-89837307 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:94451803-94451993 | Common:3; Rare:58 | ||||
| chr4:98143459-98143638 | Common:1; Rare:44 | ||||
| chr4:98261142-98261550 | Common:1; Rare:140 | ||||
| chr4:98929101-98929365 | Common:3; Rare:66 | ||||
| chr4:98995356-98995748 | Common:6; Rare:136 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99321311-99321551 | Rare:52 | ||||
| chr4:99352941-99353163 | Common:2; Rare:52 | ||||
| chr4:99563562-99563803 | Common:2; Rare:69 | ||||
| chr4:99563989-99564127 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894357-99894620 | Common:3; Rare:91 | ||||
| chr4:99946557-99946812 | Rare:90 | ||||
| chr4:99950243-99950467 | Rare:46 | ||||
| chr4:101346835-101347121 | Common:2; Rare:69 |