| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52517588-52517994 | Common:1; Rare:112; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:52519422-52519739 | Common:4; Rare:67; Clinvar (benign):1 | ||||
| chr12:52520424-52520582 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr12:52905032-52905278 | Common:2; Rare:62 | ||||
| chr12:52948787-52949093 | Common:2; Rare:64 | ||||
| chr12:53006117-53006489 | Common:4; Rare:134 | ||||
| chr12:53049948-53050081 | Rare:41 | ||||
| chr12:53079335-53079568 | Common:2; Rare:80 | ||||
| chr12:53097546-53097682 | Rare:37 | ||||
| chr12:53180625-53180709 | Common:1; Rare:25 | ||||
| chr12:53231930-53231948 | Rare:8 | ||||
| chr12:53232179-53232479 | Common:3; Rare:65 | ||||
| chr12:53232764-53233035 | Rare:37 | ||||
| chr12:53252049-53252212 | Common:3; Rare:62 | ||||
| chr12:53295443-53295608 | Common:1; Rare:61 |