| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105825-48105938 | Rare:26 | ||||
| chr12:48105964-48106139 | Common:1; Rare:52 | ||||
| chr12:48350771-48350963 | Rare:68 | ||||
| chr12:48351247-48351332 | Common:1; Rare:16 | ||||
| chr12:48716679-48716941 | Common:4; Rare:82 | ||||
| chr12:48814747-48814862 | Rare:20 | ||||
| chr12:48815465-48815612 | Common:1; Rare:33 | ||||
| chr12:48818492-48818505 | Rare:6 | ||||
| chr12:48852086-48852189 | Rare:41 | ||||
| chr12:49018738-49018908 | Rare:68 | ||||
| chr12:49130673-49130914 | Common:4; Rare:80 | ||||
| chr12:49131299-49131617 | Common:2; Rare:125 | ||||
| chr12:49188482-49188655 | Common:2; Rare:23 | ||||
| chr12:49188975-49189131 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49189176-49189356 | Rare:38 |