| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:29280822-29280920 | Common:1; Rare:19 | ||||
| chr3:29280949-29281754 | Common:15; Rare:168 | ||||
| chr3:30606291-30606636 | Common:1; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:30606701-30606984 | Common:1; Rare:85; Clinvar:5; Clinvar (benign):6 | ||||
| chr3:31532371-31532728 | Common:4; Rare:110 | ||||
| chr3:31533016-31533310 | Common:1; Rare:90; Clinvar (benign):2 | ||||
| chr3:31981627-31981803 | Common:1; Rare:44 | ||||
| chr3:32106402-32106720 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32238537-32238905 | Common:2; Rare:101 | ||||
| chr3:32570640-32570970 | Common:1; Rare:145 | ||||
| chr3:32685051-32685386 | Rare:102 | ||||
| chr3:32951491-32951647 | Common:1; Rare:40 | ||||
| chr3:33097070-33097233 | Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33114274-33114405 | Common:1; Rare:40; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:33218793-33218981 | Common:3; Rare:56 |