| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55716391-55716601 | Common:3; Rare:56 | ||||
| chr12:55728932-55729250 | Rare:68 | ||||
| chr12:55729657-55729827 | Rare:41 | ||||
| chr12:55829497-55829793 | Rare:92 | ||||
| chr12:55830525-55830932 | Common:1; Rare:108 | ||||
| chr12:55927763-55927968 | Rare:58 | ||||
| chr12:55931938-55932101 | Rare:42 | ||||
| chr12:55966037-55966291 | Common:1; Rare:51 | ||||
| chr12:55966700-55966843 | Rare:36 | ||||
| chr12:55997067-55997370 | Common:2; Rare:82; Clinvar:2 | ||||
| chr12:56007617-56007871 | Common:2; Rare:61 | ||||
| chr12:56020795-56021086 | Rare:47 | ||||
| chr12:56021228-56021379 | Common:9; Rare:23 | ||||
| chr12:56041561-56041984 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr12:56079877-56080222 | Common:4; Rare:76 |