| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348793-28349188 | Common:4; Rare:123 | ||||
| chr3:29280791-29281102 | Common:4; Rare:62 | ||||
| chr3:30606341-30606592 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:31532380-31532662 | Common:4; Rare:81 | ||||
| chr3:31533016-31533301 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:31981624-31981776 | Rare:42 | ||||
| chr3:32570625-32571046 | Common:1; Rare:180 | ||||
| chr3:33440397-33440552 | Common:1; Rare:40 | ||||
| chr3:33718211-33718292 | Rare:39 | ||||
| chr3:33798228-33798923 | Common:5; Rare:210 | ||||
| chr3:33798985-33799039 | Rare:17 | ||||
| chr3:36908489-36908664 | Rare:38 | ||||
| chr3:36993077-36993572 | Common:2; Rare:171; Clinvar:28; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr3:37176104-37176460 | Common:2; Rare:104 | ||||
| chr3:37243116-37243578 | Common:3; Rare:131 |