| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48774719-48774960 | Common:1; Rare:55 | ||||
| chr12:48814679-48814882 | Rare:39 | ||||
| chr12:48815428-48815631 | Common:1; Rare:45 | ||||
| chr12:48839874-48840074 | Rare:52 | ||||
| chr12:48852086-48852363 | Common:2; Rare:83 | ||||
| chr12:48957236-48957585 | Common:3; Rare:94 | ||||
| chr12:49018735-49018888 | Rare:64 | ||||
| chr12:49130604-49130912 | Common:4; Rare:93 | ||||
| chr12:49131298-49131621 | Common:2; Rare:126 | ||||
| chr12:49188506-49188583 | Common:1; Rare:12 | ||||
| chr12:49188998-49189175 | Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265105 | Common:4; Rare:118 | ||||
| chr12:49322980-49323307 | Common:3; Rare:77 | ||||
| chr12:49367234-49367530 | Common:1; Rare:79 | ||||
| chr12:49568089-49568211 | Common:2; Rare:44 |