| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55729650-55729828 | Rare:42 | ||||
| chr12:55829500-55829799 | Rare:93 | ||||
| chr12:55830517-55830851 | Common:1; Rare:92 | ||||
| chr12:55927757-55927947 | Rare:54 | ||||
| chr12:55966031-55966294 | Common:1; Rare:52 | ||||
| chr12:55966680-55966896 | Rare:58 | ||||
| chr12:55973583-55973817 | Common:1; Rare:59 | ||||
| chr12:55997127-55997337 | Common:1; Rare:64; Clinvar:2 | ||||
| chr12:56007616-56007881 | Common:2; Rare:65 | ||||
| chr12:56020795-56021086 | Rare:47 | ||||
| chr12:56021663-56021754 | Common:2; Rare:3 | ||||
| chr12:56041554-56041972 | Common:4; Rare:89; Clinvar (benign):1 | ||||
| chr12:56104196-56104749 | Common:5; Rare:186 | ||||
| chr12:56116523-56116825 | Common:2; Rare:116 | ||||
| chr12:56117978-56118339 | Common:1; Rare:113 |