| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:20369540-20370122 | Common:4; Rare:249 | ||||
| chr12:21437592-21437714 | Common:5; Rare:51 | ||||
| chr12:21501550-21501915 | Common:4; Rare:101 | ||||
| chr12:21657740-21658031 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21940930-21941439 | Rare:104 | ||||
| chr12:22544143-22544280 | Rare:67 | ||||
| chr12:22544470-22544681 | Common:2; Rare:47 | ||||
| chr12:22625044-22625235 | Rare:106 | ||||
| chr12:23949664-23949841 | Common:4; Rare:27 | ||||
| chr12:25195077-25195325 | Common:2; Rare:80 | ||||
| chr12:25959371-25959621 | Common:2; Rare:42 | ||||
| chr12:26833146-26833505 | Common:2; Rare:100 | ||||
| chr12:26937961-26938552 | Common:11; Rare:198 | ||||
| chr12:27244058-27244325 | Common:2; Rare:85 | ||||
| chr12:27523989-27524282 | Rare:67 |