| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55930623-55930642 | Rare:4 | ||||
| chr12:55931324-55931508 | Common:2; Rare:26 | ||||
| chr12:55931947-55932117 | Rare:43 | ||||
| chr12:55966698-55966870 | Rare:46 | ||||
| chr12:56079769-56079890 | Rare:29 | ||||
| chr12:56079991-56080329 | Common:4; Rare:89 | ||||
| chr12:56087848-56088173 | Common:2; Rare:88; Clinvar (pathogenic):1 | ||||
| chr12:56104346-56104670 | Common:4; Rare:111 | ||||
| chr12:56116497-56116833 | Common:2; Rare:129 | ||||
| chr12:56117929-56118278 | Rare:113 | ||||
| chr12:56152461-56152626 | Rare:51 | ||||
| chr12:56158223-56158403 | Rare:61 | ||||
| chr12:56161954-56162236 | Rare:59 | ||||
| chr12:56181536-56181832 | Rare:73 | ||||
| chr12:56221846-56222042 | Common:1; Rare:53 |