| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916898-23917208 | Rare:122 | ||||
| chr3:25428106-25428272 | Rare:32 | ||||
| chr3:25783392-25783616 | Common:2; Rare:74; Clinvar (benign):3 | ||||
| chr3:28348618-28348711 | Rare:21 | ||||
| chr3:28348779-28349188 | Common:4; Rare:128 | ||||
| chr3:29280837-29281076 | Common:3; Rare:48 | ||||
| chr3:32106408-32106674 | Common:4; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570766-32570992 | Common:1; Rare:98 | ||||
| chr3:33218800-33218987 | Common:3; Rare:56 | ||||
| chr3:33277312-33277482 | Common:1; Rare:45 | ||||
| chr3:33798560-33798669 | Common:2; Rare:43 | ||||
| chr3:36993171-36993563 | Common:2; Rare:118; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176237-37176395 | Rare:52 | ||||
| chr3:37243166-37243341 | Common:1; Rare:48 | ||||
| chr3:38029612-38029796 | Common:1; Rare:36 |