| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107477-39107741 | Common:4; Rare:86 | ||||
| chr3:39153540-39153856 | Common:6; Rare:97 | ||||
| chr3:39154539-39154697 | Rare:37 | ||||
| chr3:39383258-39383439 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383567-39383668 | Rare:22; Clinvar:1 | ||||
| chr3:39406593-39407101 | Common:6; Rare:196 | ||||
| chr3:40309486-40309830 | Common:9; Rare:119 | ||||
| chr3:40457204-40457381 | Common:3; Rare:86 | ||||
| chr3:40477094-40477184 | Common:1; Rare:25 | ||||
| chr3:40524815-40525019 | Common:1; Rare:60 | ||||
| chr3:41199380-41199653 | Common:1; Rare:108 | ||||
| chr3:42160073-42160348 | Common:3; Rare:66 | ||||
| chr3:42581848-42582141 | Common:4; Rare:92 | ||||
| chr3:42600422-42600710 | Common:2; Rare:110 | ||||
| chr3:42804427-42804646 | Common:2; Rare:65 |