| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48852127-48852397 | Common:2; Rare:69 | ||||
| chr12:48957317-48957642 | Common:4; Rare:91 | ||||
| chr12:49018737-49018926 | Rare:78 | ||||
| chr12:49110840-49111045 | Rare:49 | ||||
| chr12:49131299-49131621 | Common:2; Rare:126 | ||||
| chr12:49188981-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322980-49323303 | Common:3; Rare:74 | ||||
| chr12:49367159-49367548 | Common:1; Rare:109 | ||||
| chr12:49568078-49568211 | Common:2; Rare:47 | ||||
| chr12:49828380-49828571 | Common:1; Rare:69 | ||||
| chr12:50085031-50085543 | Common:1; Rare:128 | ||||
| chr12:50283452-50283664 | Common:2; Rare:64 | ||||
| chr12:50504926-50505123 | Common:3; Rare:97 | ||||
| chr12:50763950-50764297 | Common:1; Rare:91 | ||||
| chr12:51026313-51026508 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 |