| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48852111-48852291 | Common:2; Rare:57 | ||||
| chr12:48957367-48957559 | Common:2; Rare:53 | ||||
| chr12:49018741-49018908 | Rare:65 | ||||
| chr12:49110661-49110796 | Rare:30 | ||||
| chr12:49110797-49111058 | Rare:61 | ||||
| chr12:49131299-49131614 | Common:2; Rare:125 | ||||
| chr12:49188488-49188595 | Common:1; Rare:15 | ||||
| chr12:49188975-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49568089-49568211 | Common:2; Rare:44 | ||||
| chr12:49741268-49741598 | Rare:92 | ||||
| chr12:49828387-49828552 | Common:1; Rare:59 | ||||
| chr12:49843092-49843187 | Common:1; Rare:34 | ||||
| chr12:49903856-49904086 | Common:2; Rare:60 | ||||
| chr12:50025444-50025739 | Common:2; Rare:78 | ||||
| chr12:50085040-50085364 | Common:1; Rare:85 |