| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003605-95003835 | Common:3; Rare:97; Clinvar (benign):6 | ||||
| chr12:95025195-95025305 | Rare:27 | ||||
| chr12:95073387-95073965 | Common:4; Rare:144 | ||||
| chr12:95217219-95217877 | Common:6; Rare:192 | ||||
| chr12:95218156-95218323 | Common:2; Rare:41 | ||||
| chr12:95474044-95474330 | Common:2; Rare:118 | ||||
| chr12:95476034-95476423 | Common:2; Rare:85 | ||||
| chr12:95548792-95548914 | Common:2; Rare:43 | ||||
| chr12:95791113-95791509 | Rare:69 | ||||
| chr12:95858822-95859073 | Common:3; Rare:73 | ||||
| chr12:95943217-95943341 | Rare:20 | ||||
| chr12:96035352-96035386 | Rare:9 | ||||
| chr12:96035485-96035731 | Common:2; Rare:59 | ||||
| chr12:96194260-96194622 | Common:4; Rare:119 | ||||
| chr12:96907147-96907303 | Common:1; Rare:57 |