| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:95548913-95549114 | Common:1; Rare:45 | ||||
| chr4:95549203-95549390 | Common:1; Rare:32 | ||||
| chr4:98143247-98143638 | Common:1; Rare:87 | ||||
| chr4:98261142-98261547 | Common:1; Rare:139 | ||||
| chr4:98929101-98929401 | Common:3; Rare:73 | ||||
| chr4:98995427-98995774 | Common:6; Rare:126 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99208825-99209110 | Common:2; Rare:71 | ||||
| chr4:99563510-99563805 | Common:2; Rare:84 | ||||
| chr4:99563974-99564143 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99816616-99816867 | Common:1; Rare:34 | ||||
| chr4:99894351-99894613 | Common:2; Rare:92 | ||||
| chr4:99946534-99946992 | Common:1; Rare:148 | ||||
| chr4:99950261-99950560 | Rare:68 | ||||
| chr4:101347602-101347826 | Common:4; Rare:65 |