| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56687969-56688586 | Common:5; Rare:225 | ||||
| chr12:56724955-56725477 | Common:3; Rare:136 | ||||
| chr12:56725484-56725610 | Rare:29 | ||||
| chr12:56752294-56752483 | Rare:61 | ||||
| chr12:57087832-57087984 | Common:1; Rare:40 | ||||
| chr12:57089083-57089352 | Rare:89 | ||||
| chr12:57098617-57098799 | Rare:51 | ||||
| chr12:57111133-57111453 | Common:4; Rare:58 | ||||
| chr12:57128390-57128767 | Common:1; Rare:70 | ||||
| chr12:57229572-57229796 | Common:3; Rare:93 | ||||
| chr12:57230007-57230407 | Rare:81 | ||||
| chr12:57232452-57232837 | Common:2; Rare:112 | ||||
| chr12:57240720-57240783 | Rare:9 | ||||
| chr12:57430722-57431102 | Common:2; Rare:97 | ||||
| chr12:57489919-57490377 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):3 |