| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46362777-46363085 | Rare:65 | ||||
| chr12:46370509-46370822 | Rare:71 | ||||
| chr12:46372651-46372953 | Rare:128 | ||||
| chr12:47705960-47706126 | Rare:71 | ||||
| chr12:48852116-48852382 | Common:2; Rare:73 | ||||
| chr12:49018734-49018963 | Common:1; Rare:93 | ||||
| chr12:49131376-49131569 | Rare:66 | ||||
| chr12:49188875-49188948 | Common:1; Rare:16 | ||||
| chr12:49188991-49189399 | Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265090 | Common:4; Rare:112 | ||||
| chr12:49568110-49568188 | Common:2; Rare:25 | ||||
| chr12:49828374-49828543 | Common:1; Rare:64 | ||||
| chr12:50924476-50924759 | Common:3; Rare:83 | ||||
| chr12:51009211-51009356 | Common:1; Rare:27 | ||||
| chr12:51048077-51048368 | Common:2; Rare:102 |