| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30754762-30755041 | Common:1; Rare:112 | ||||
| chr12:31073716-31073902 | Common:8; Rare:65 | ||||
| chr12:31324046-31324270 | Rare:66 | ||||
| chr12:31326083-31326428 | Common:3; Rare:103 | ||||
| chr12:31659105-31659258 | Common:1; Rare:46 | ||||
| chr12:31728995-31729313 | Common:1; Rare:101 | ||||
| chr12:31959250-31959487 | Common:2; Rare:77 | ||||
| chr12:32106572-32106875 | Common:4; Rare:84 | ||||
| chr12:32755878-32755922 | Rare:16 | ||||
| chr12:32821754-32821963 | Common:1; Rare:45 | ||||
| chr12:32896513-32896990 | Common:6; Rare:157; Clinvar:18; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr12:38905526-38905670 | Common:3; Rare:41 | ||||
| chr12:39619722-39620101 | Common:2; Rare:60 | ||||
| chr12:42238164-42238562 | Common:5; Rare:125 | ||||
| chr12:42325927-42326212 | Common:1; Rare:89 |