| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94207836-94208095 | Common:2; Rare:98 | ||||
| chr4:94757860-94758030 | Common:3; Rare:48 | ||||
| chr4:98261148-98261472 | Common:1; Rare:106 | ||||
| chr4:98657647-98657763 | Rare:27 | ||||
| chr4:98658579-98658916 | Common:2; Rare:97 | ||||
| chr4:98929015-98929212 | Common:3; Rare:70 | ||||
| chr4:98995633-98995815 | Rare:70 | ||||
| chr4:99088660-99088943 | Common:7; Rare:133 | ||||
| chr4:99563593-99563760 | Common:2; Rare:49 | ||||
| chr4:99563986-99564093 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr4:99894343-99894621 | Common:3; Rare:96 | ||||
| chr4:99949722-99949987 | Common:3; Rare:93 | ||||
| chr4:99950218-99950538 | Common:1; Rare:81 | ||||
| chr4:100190440-100190573 | Common:2; Rare:33 | ||||
| chr4:101347507-101347840 | Common:5; Rare:101 |