| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188447-49188655 | Common:2; Rare:27 | ||||
| chr12:49188981-49189222 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265092 | Common:5; Rare:120 | ||||
| chr12:49367235-49367530 | Common:1; Rare:79 | ||||
| chr12:49568104-49568223 | Common:2; Rare:38 | ||||
| chr12:49623284-49623571 | Common:1; Rare:80 | ||||
| chr12:49828324-49828600 | Common:1; Rare:100 | ||||
| chr12:50025407-50025741 | Common:2; Rare:87 | ||||
| chr12:50085132-50085399 | Common:1; Rare:75 | ||||
| chr12:50283481-50283672 | Common:3; Rare:61 | ||||
| chr12:50763953-50764282 | Common:1; Rare:89 | ||||
| chr12:50924475-50924745 | Common:3; Rare:79 | ||||
| chr12:51048074-51048359 | Common:2; Rare:95 | ||||
| chr12:51239133-51239306 | Common:2; Rare:51 | ||||
| chr12:51270278-51270708 | Common:8; Rare:105 |