| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16769-17048 | Common:9; Rare:82 | ||||
| chr12:1581790-1582108 | Rare:59 | ||||
| chr12:1710458-1710618 | Common:2; Rare:42 | ||||
| chr12:2584426-2584550 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:2797461-2797788 | Common:1; Rare:78 | ||||
| chr12:4726309-4726600 | Rare:53 | ||||
| chr12:4735432-4735601 | Rare:33 | ||||
| chr12:4735644-4735851 | Rare:30 | ||||
| chr12:6233153-6233486 | Common:1; Rare:73 | ||||
| chr12:6235114-6235327 | Common:1; Rare:61 | ||||
| chr12:6315336-6315647 | Common:4; Rare:69 | ||||
| chr12:6321819-6322091 | Common:1; Rare:49 | ||||
| chr12:6322592-6322863 | Common:2; Rare:58 | ||||
| chr12:6323491-6323524 | Rare:6 | ||||
| chr12:6324224-6324563 | Common:3; Rare:69 |