| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601516-15601810 | Common:4; Rare:125; Clinvar:2 | ||||
| chr3:16264881-16265209 | Common:2; Rare:106 | ||||
| chr3:19946978-19947350 | Common:5; Rare:137 | ||||
| chr3:21751184-21751405 | Common:3; Rare:64 | ||||
| chr3:23202930-23203126 | Common:1; Rare:71 | ||||
| chr3:23805791-23806061 | Common:2; Rare:53 | ||||
| chr3:23916905-23917204 | Rare:115 | ||||
| chr3:25428099-25428316 | Rare:42 | ||||
| chr3:25783392-25783660 | Common:2; Rare:81; Clinvar (benign):3 | ||||
| chr3:28349007-28349178 | Common:2; Rare:49 | ||||
| chr3:29280831-29281079 | Common:3; Rare:48 | ||||
| chr3:30606401-30606522 | Common:1; Rare:27; Clinvar:1 | ||||
| chr3:32570766-32571142 | Common:3; Rare:142 | ||||
| chr3:33277294-33277476 | Common:2; Rare:46 | ||||
| chr3:33798290-33798664 | Common:3; Rare:105 |