| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45990478-45990966 | Common:3; Rare:159 | ||||
| chr12:45992049-45992083 | Common:1; Rare:5 | ||||
| chr12:46268699-46269221 | Common:2; Rare:135 | ||||
| chr12:46269653-46269952 | Rare:58 | ||||
| chr12:46372679-46372956 | Rare:118 | ||||
| chr12:47079511-47079651 | Common:1; Rare:27 | ||||
| chr12:47079771-47080074 | Common:4; Rare:75 | ||||
| chr12:47705960-47706099 | Rare:62 | ||||
| chr12:47758465-47758545 | Rare:19 | ||||
| chr12:47758800-47759011 | Common:1; Rare:42 | ||||
| chr12:48105815-48105943 | Rare:31 | ||||
| chr12:48106033-48106202 | Common:2; Rare:61 | ||||
| chr12:48119192-48119398 | Common:2; Rare:42; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48184028-48184242 | Common:2; Rare:77 | ||||
| chr12:48350787-48351118 | Common:6; Rare:120 |