| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48852113-48852335 | Common:2; Rare:66 | ||||
| chr12:49018739-49018908 | Rare:67 | ||||
| chr12:49131301-49131648 | Common:2; Rare:138 | ||||
| chr12:49188506-49188615 | Common:2; Rare:15 | ||||
| chr12:49188981-49189193 | Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264757-49265136 | Common:4; Rare:137 | ||||
| chr12:49322986-49323323 | Common:3; Rare:76 | ||||
| chr12:49367171-49367534 | Common:1; Rare:102 | ||||
| chr12:49568104-49568170 | Common:1; Rare:22 | ||||
| chr12:49758245-49758443 | Common:4; Rare:60 | ||||
| chr12:49828362-49828579 | Common:1; Rare:82 | ||||
| chr12:50283507-50283638 | Rare:38 | ||||
| chr12:50400749-50400946 | Rare:60 | ||||
| chr12:51048142-51048359 | Common:1; Rare:77 | ||||
| chr12:51238661-51238890 | Common:8; Rare:102 |