| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:81761504-81761799 | Common:8; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227201-87227510 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058914-88059380 | Common:3; Rare:175 | ||||
| chr3:88149605-88150011 | Common:1; Rare:105 | ||||
| chr3:93979918-93980201 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062887-94063097 | Rare:52 | ||||
| chr3:97764478-97764814 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821833-97822074 | Rare:86 | ||||
| chr3:98817561-98817889 | Common:2; Rare:68 | ||||
| chr3:98900693-98900986 | Rare:60 | ||||
| chr3:98900996-98901052 | Rare:13 | ||||
| chr3:98901121-98901180 | Common:1; Rare:22 | ||||
| chr3:98901621-98902102 | Common:1; Rare:175 | ||||
| chr3:99817811-99818043 | Rare:79 | ||||
| chr3:100334658-100334792 | Common:1; Rare:59 |