| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50401275-50401433 | Common:1; Rare:33 | ||||
| chr12:50504830-50505174 | Common:4; Rare:137 | ||||
| chr12:50505198-50505356 | Rare:33 | ||||
| chr12:50763447-50763762 | Common:5; Rare:58 | ||||
| chr12:50763795-50764148 | Common:2; Rare:102 | ||||
| chr12:50764283-50764616 | Common:4; Rare:115 | ||||
| chr12:50764715-50764859 | Common:1; Rare:35 | ||||
| chr12:50764889-50765156 | Rare:55 | ||||
| chr12:51005769-51006003 | Rare:34 | ||||
| chr12:51024927-51025181 | Common:1; Rare:44 | ||||
| chr12:51025761-51025794 | Rare:8 | ||||
| chr12:51025796-51025966 | Common:1; Rare:31 | ||||
| chr12:51026082-51026290 | Common:1; Rare:51 | ||||
| chr12:51026300-51026687 | Common:6; Rare:134; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51028181-51028409 | Rare:53 |