| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94757754-94758061 | Common:4; Rare:80 | ||||
| chr4:95548921-95549116 | Common:1; Rare:44 | ||||
| chr4:98143448-98143628 | Common:1; Rare:42 | ||||
| chr4:98261152-98261499 | Common:1; Rare:107 | ||||
| chr4:98929105-98929378 | Common:3; Rare:68 | ||||
| chr4:98995491-98995794 | Common:6; Rare:106 | ||||
| chr4:99088696-99088884 | Common:6; Rare:85 | ||||
| chr4:99563593-99563770 | Common:2; Rare:49 | ||||
| chr4:99563989-99564144 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894344-99894620 | Common:3; Rare:96 | ||||
| chr4:99950223-99950535 | Rare:74 | ||||
| chr4:101346762-101347060 | Common:2; Rare:79 | ||||
| chr4:101347579-101347870 | Common:4; Rare:82 | ||||
| chr4:101348036-101348163 | Rare:37 | ||||
| chr4:102826740-102827200 | Common:4; Rare:151 |