| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55728932-55729230 | Rare:66 | ||||
| chr12:55729418-55729807 | Common:2; Rare:78 | ||||
| chr12:55829491-55829802 | Rare:96 | ||||
| chr12:55830739-55831031 | Common:2; Rare:89 | ||||
| chr12:55842910-55843010 | Rare:20 | ||||
| chr12:55927759-55927951 | Rare:53 | ||||
| chr12:55931894-55932101 | Rare:51 | ||||
| chr12:55966700-55966863 | Rare:41 | ||||
| chr12:56041608-56041972 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr12:56079980-56080213 | Common:4; Rare:58 | ||||
| chr12:56104367-56104668 | Common:4; Rare:106 | ||||
| chr12:56116309-56116806 | Common:3; Rare:174 | ||||
| chr12:56116906-56117236 | Common:4; Rare:90 | ||||
| chr12:56117982-56118305 | Rare:103 | ||||
| chr12:56152460-56152630 | Rare:52 |