| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54259534-54259655 | Rare:24 | ||||
| chr12:55682136-55682251 | Common:1; Rare:30 | ||||
| chr12:55688931-55689155 | Common:2; Rare:55; Clinvar:3 | ||||
| chr12:55689193-55689305 | Common:1; Rare:13 | ||||
| chr12:55716014-55716207 | Common:1; Rare:86 | ||||
| chr12:55716771-55716977 | Rare:51 | ||||
| chr12:55720210-55720514 | Common:4; Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55728946-55729135 | Rare:35 | ||||
| chr12:55729657-55729996 | Rare:68 | ||||
| chr12:55829500-55829804 | Rare:95 | ||||
| chr12:55931948-55932063 | Rare:33 | ||||
| chr12:55966697-55966892 | Rare:51 | ||||
| chr12:55997104-55997337 | Common:1; Rare:67; Clinvar:2 | ||||
| chr12:56041614-56041972 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr12:56079973-56080213 | Common:4; Rare:59 |