| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50167298-50167648 | Common:3; Rare:100 | ||||
| chr12:50283508-50283621 | Rare:30 | ||||
| chr12:50400716-50400968 | Rare:76 | ||||
| chr12:50763937-50764297 | Common:1; Rare:92 | ||||
| chr12:51026325-51026524 | Common:3; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048090-51048359 | Common:2; Rare:92 | ||||
| chr12:51172780-51172905 | Common:2; Rare:29 | ||||
| chr12:51173061-51173225 | Rare:31 | ||||
| chr12:51238666-51238899 | Common:5; Rare:103 | ||||
| chr12:51270278-51270442 | Common:3; Rare:46 | ||||
| chr12:51391611-51391736 | Common:1; Rare:39 | ||||
| chr12:52051143-52051448 | Common:1; Rare:100 | ||||
| chr12:52191822-52192072 | Common:3; Rare:80 | ||||
| chr12:52244048-52244458 | Common:4; Rare:75 | ||||
| chr12:52905036-52905285 | Common:2; Rare:62 |