| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:89107529-89107796 | Common:2; Rare:80 | ||||
| chr3:93979912-93980190 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062897-94063069 | Rare:44 | ||||
| chr3:96814388-96814650 | Rare:101 | ||||
| chr3:97764454-97764821 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97972395-97972509 | Common:3; Rare:44 | ||||
| chr3:98522858-98523098 | Common:1; Rare:73 | ||||
| chr3:99817562-99817924 | Rare:105 | ||||
| chr3:99876136-99876278 | Common:1; Rare:35 | ||||
| chr3:100260691-100261048 | Rare:101 | ||||
| chr3:100401402-100401602 | Common:1; Rare:36 | ||||
| chr3:100492455-100492626 | Common:1; Rare:57 | ||||
| chr3:101513110-101513306 | Common:8; Rare:41 | ||||
| chr3:101561743-101561991 | Common:2; Rare:89 | ||||
| chr3:101574053-101574233 | Rare:60 |