| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47758696-47759011 | Common:1; Rare:57 | ||||
| chr12:48105846-48105948 | Rare:27 | ||||
| chr12:48105985-48106200 | Common:2; Rare:70 | ||||
| chr12:48350785-48350956 | Rare:65 | ||||
| chr12:48774734-48775006 | Common:1; Rare:59 | ||||
| chr12:49018735-49018908 | Rare:69 | ||||
| chr12:49188455-49188590 | Common:1; Rare:19 | ||||
| chr12:49568077-49568399 | Common:2; Rare:82 | ||||
| chr12:49623254-49623571 | Common:1; Rare:90 | ||||
| chr12:49828392-49828553 | Common:1; Rare:54 | ||||
| chr12:50283481-50283621 | Rare:42 | ||||
| chr12:50763953-50764128 | Common:1; Rare:50 | ||||
| chr12:51026321-51026510 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048103-51048366 | Common:2; Rare:92 | ||||
| chr12:51173061-51173256 | Rare:37 |