| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:94062689-94063137 | Common:4; Rare:111 | ||||
| chr3:94063210-94063374 | Rare:34 | ||||
| chr3:97764328-97764821 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821868-97822114 | Rare:90 | ||||
| chr3:97971934-97972198 | Rare:61 | ||||
| chr3:97972339-97972534 | Common:3; Rare:79 | ||||
| chr3:98522563-98522693 | Rare:31 | ||||
| chr3:98522783-98523169 | Common:2; Rare:129 | ||||
| chr3:98531673-98532033 | Common:2; Rare:86 | ||||
| chr3:98593571-98593895 | Common:2; Rare:108 | ||||
| chr3:98732200-98732328 | Rare:21 | ||||
| chr3:98733702-98733843 | Common:1; Rare:34 | ||||
| chr3:98901628-98902109 | Common:2; Rare:176 | ||||
| chr3:99817533-99817925 | Common:1; Rare:119 | ||||
| chr3:99818071-99818160 | Common:1; Rare:23 |