| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50763925-50764128 | Common:1; Rare:57 | ||||
| chr12:51026328-51026542 | Common:3; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048119-51048353 | Common:1; Rare:79 | ||||
| chr12:51238637-51238915 | Common:8; Rare:116 | ||||
| chr12:51270278-51270439 | Common:3; Rare:45 | ||||
| chr12:51391600-51391737 | Common:1; Rare:41 | ||||
| chr12:51887981-51888141 | Common:1; Rare:40 | ||||
| chr12:51912229-51912446 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr12:51915937-51916130 | Rare:55; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr12:52949776-52950033 | Rare:59 | ||||
| chr12:53079365-53079530 | Common:2; Rare:56 | ||||
| chr12:53295423-53295591 | Common:1; Rare:56 | ||||
| chr12:53501189-53501352 | Rare:39 | ||||
| chr12:53625942-53626137 | Common:1; Rare:47 | ||||
| chr12:54259534-54259655 | Rare:24 |