| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50025412-50025747 | Common:2; Rare:91 | ||||
| chr12:50085020-50085355 | Rare:88 | ||||
| chr12:50112049-50112263 | Common:2; Rare:49 | ||||
| chr12:50400716-50400968 | Rare:76 | ||||
| chr12:50763920-50764113 | Common:1; Rare:56 | ||||
| chr12:50924459-50924722 | Common:3; Rare:77 | ||||
| chr12:51026328-51026496 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048111-51048353 | Common:2; Rare:80 | ||||
| chr12:51238637-51238885 | Common:8; Rare:104 | ||||
| chr12:52037105-52037442 | Common:1; Rare:99 | ||||
| chr12:53006133-53006494 | Common:4; Rare:128 | ||||
| chr12:53079375-53079568 | Common:2; Rare:59 | ||||
| chr12:53180625-53180763 | Common:1; Rare:50 | ||||
| chr12:53180905-53181146 | Common:4; Rare:67 | ||||
| chr12:53252049-53252203 | Common:3; Rare:59 |