| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188061-49188436 | Common:1; Rare:133 | ||||
| chr12:49188493-49188814 | Common:5; Rare:125 | ||||
| chr12:49188963-49189353 | Rare:279; Clinvar:6; Clinvar (benign):6 | ||||
| chr12:49264648-49265340 | Common:17; Rare:579 | ||||
| chr12:49265376-49265780 | Common:4; Rare:148 | ||||
| chr12:49297429-49297750 | Common:14; Rare:278; Clinvar:14 | ||||
| chr12:49322864-49323368 | Common:13; Rare:341 | ||||
| chr12:49346573-49347513 | Common:10; Rare:283 | ||||
| chr12:49366616-49367050 | Common:4; Rare:229 | ||||
| chr12:49367080-49367582 | Common:5; Rare:354 | ||||
| chr12:49538592-49539085 | Rare:274 | ||||
| chr12:49567680-49568500 | Common:6; Rare:438 | ||||
| chr12:49622929-49623090 | Rare:47 | ||||
| chr12:49623196-49623613 | Common:6; Rare:321 | ||||
| chr12:49707393-49707689 | Common:2; Rare:91 |