| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:29280810-29280916 | Common:1; Rare:21 | ||||
| chr3:29280927-29280994 | Common:1; Rare:16 | ||||
| chr3:29280997-29281393 | Common:13; Rare:73 | ||||
| chr3:30606296-30606546 | Common:1; Rare:63; Clinvar:2 | ||||
| chr3:30606590-30606984 | Common:1; Rare:118; Clinvar:6; Clinvar (benign):6 | ||||
| chr3:31532396-31532733 | Common:4; Rare:99 | ||||
| chr3:32106401-32106720 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570636-32570915 | Rare:132 | ||||
| chr3:33097090-33097265 | Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277289-33277495 | Common:2; Rare:57 | ||||
| chr3:33440931-33441088 | Rare:31 | ||||
| chr3:33659506-33659652 | Rare:29 | ||||
| chr3:33718025-33718308 | Rare:104 | ||||
| chr3:33798479-33798686 | Common:2; Rare:76 | ||||
| chr3:33798985-33799163 | Rare:56 |