| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50167284-50167648 | Common:3; Rare:105 | ||||
| chr12:50283496-50283642 | Rare:43 | ||||
| chr12:50400716-50400968 | Rare:76 | ||||
| chr12:50763889-50764145 | Common:2; Rare:74 | ||||
| chr12:50924504-50924700 | Common:3; Rare:70 | ||||
| chr12:51026313-51026487 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048160-51048370 | Common:1; Rare:81 | ||||
| chr12:51238668-51238914 | Common:4; Rare:106 | ||||
| chr12:51239130-51239306 | Common:2; Rare:51 | ||||
| chr12:51270278-51270288 | Rare:1 | ||||
| chr12:51270358-51270431 | Common:1; Rare:21 | ||||
| chr12:51391611-51391752 | Common:1; Rare:43 | ||||
| chr12:51912272-51912400 | Rare:31 | ||||
| chr12:52051093-52051478 | Common:1; Rare:135 | ||||
| chr12:52905048-52905320 | Common:3; Rare:62 |