| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99563530-99563930 | Common:4; Rare:223 | ||||
| chr4:99563983-99564143 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):4 | ||||
| chr4:99894357-99894621 | Common:3; Rare:91 | ||||
| chr4:99946533-99946754 | Rare:149 | ||||
| chr4:99949690-99949981 | Common:6; Rare:174 | ||||
| chr4:99950087-99950562 | Common:2; Rare:227 | ||||
| chr4:101347388-101347823 | Common:8; Rare:216 | ||||
| chr4:102344815-102345684 | Common:6; Rare:308 | ||||
| chr4:102345892-102346037 | Common:1; Rare:14 | ||||
| chr4:102500750-102501082 | Common:3; Rare:122 | ||||
| chr4:102501213-102501462 | Common:2; Rare:79 | ||||
| chr4:102501450-102501780 | Rare:199 | ||||
| chr4:102760911-102761029 | Rare:42; Clinvar:1 | ||||
| chr4:102826747-102826994 | Rare:131 | ||||
| chr4:102827074-102827390 | Common:2; Rare:184 |