| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51079375-51079436 | Rare:20 | ||||
| chr12:52032428-52032662 | Rare:40 | ||||
| chr12:52046200-52046452 | Common:2; Rare:53 | ||||
| chr12:52051987-52052110 | Common:1; Rare:19 | ||||
| chr12:52057486-52057713 | Rare:61 | ||||
| chr12:53056839-53057067 | Rare:64 | ||||
| chr12:53123259-53123466 | Common:1; Rare:33 | ||||
| chr12:53182615-53182716 | Common:2; Rare:15 | ||||
| chr12:53307117-53307587 | Common:5; Rare:128; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:53445761-53445924 | Rare:18 | ||||
| chr12:53469162-53469242 | Common:1; Rare:16 | ||||
| chr12:53474732-53474834 | Rare:26 | ||||
| chr12:54282725-54282899 | Rare:52 | ||||
| chr12:55832279-55832359 | Rare:16 | ||||
| chr12:56044104-56044116 | Rare:3 |