| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50283452-50283734 | Common:4; Rare:87 | ||||
| chr12:50400734-50400974 | Rare:73 | ||||
| chr12:50504821-50505046 | Common:3; Rare:92 | ||||
| chr12:50763948-50764294 | Common:1; Rare:91 | ||||
| chr12:51026337-51026510 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048228-51048353 | Common:1; Rare:55 | ||||
| chr12:51238648-51238898 | Common:8; Rare:111 | ||||
| chr12:51270272-51270355 | Common:2; Rare:22 | ||||
| chr12:51391621-51391745 | Rare:40 | ||||
| chr12:51590802-51590925 | Common:1; Rare:33 | ||||
| chr12:52051152-52051451 | Common:1; Rare:98 | ||||
| chr12:52905037-52905347 | Common:3; Rare:68 | ||||
| chr12:53180915-53181150 | Common:4; Rare:64 | ||||
| chr12:53441500-53441770 | Common:1; Rare:69 | ||||
| chr12:55728408-55728518 | Rare:21 |