| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95942840-95943049 | Common:1; Rare:46 | ||||
| chr12:95943419-95943519 | Common:1; Rare:27 | ||||
| chr12:96035516-96035803 | Common:2; Rare:65 | ||||
| chr12:96035980-96036030 | Common:2; Rare:27 | ||||
| chr12:96194196-96194630 | Common:7; Rare:138 | ||||
| chr12:96399462-96399799 | Common:1; Rare:95 | ||||
| chr12:96399977-96400015 | Rare:10 | ||||
| chr12:96400104-96400523 | Common:2; Rare:125 | ||||
| chr12:96400533-96400747 | Common:1; Rare:87 | ||||
| chr12:96489415-96489684 | Common:3; Rare:79 | ||||
| chr12:96907126-96907303 | Common:1; Rare:65 | ||||
| chr12:98515058-98515828 | Common:5; Rare:237; Clinvar:5 | ||||
| chr12:98515850-98516088 | Rare:84; Clinvar:5; Clinvar (benign):5 | ||||
| chr12:98516131-98516587 | Common:2; Rare:149 | ||||
| chr12:98593391-98593810 | Common:2; Rare:137; Clinvar:4; Clinvar (benign):4 |