| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48861184-48861330 | Rare:26 | ||||
| chr12:48865815-48866011 | Rare:59 | ||||
| chr12:48956482-48957127 | Common:5; Rare:127 | ||||
| chr12:48957348-48957711 | Common:5; Rare:98 | ||||
| chr12:48971809-48971860 | Common:3; Rare:12 | ||||
| chr12:49017995-49018160 | Rare:30 | ||||
| chr12:49018191-49018348 | Rare:26 | ||||
| chr12:49018349-49018421 | Rare:10 | ||||
| chr12:49018472-49018960 | Common:4; Rare:166 | ||||
| chr12:49019312-49019396 | Rare:9; Clinvar:1 | ||||
| chr12:49059143-49059440 | Rare:54 | ||||
| chr12:49059562-49059673 | Rare:23 | ||||
| chr12:49059889-49060067 | Rare:33 | ||||
| chr12:49060108-49060304 | Rare:67 | ||||
| chr12:49069539-49070192 | Common:8; Rare:171 |