| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:95548941-95549133 | Common:2; Rare:43 | ||||
| chr4:95549231-95549534 | Common:2; Rare:70 | ||||
| chr4:98143450-98143544 | Rare:20 | ||||
| chr4:98261148-98261539 | Common:1; Rare:131 | ||||
| chr4:98929101-98929399 | Common:3; Rare:72 | ||||
| chr4:98995356-98995765 | Common:6; Rare:140 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99291434-99291679 | Rare:47 | ||||
| chr4:99352980-99353154 | Common:2; Rare:40 | ||||
| chr4:99563591-99563764 | Common:2; Rare:49 | ||||
| chr4:99563965-99564165 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894351-99894579 | Common:1; Rare:87 | ||||
| chr4:99946551-99946764 | Rare:77 | ||||
| chr4:99950248-99950538 | Rare:66 | ||||
| chr4:101347513-101347835 | Common:5; Rare:101 |