| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53097762-53097985 | Rare:55 | ||||
| chr12:53180596-53180768 | Common:1; Rare:67 | ||||
| chr12:53181337-53181449 | Rare:28 | ||||
| chr12:53232181-53232451 | Common:2; Rare:60 | ||||
| chr12:53251856-53252208 | Common:4; Rare:128 | ||||
| chr12:53295414-53295587 | Common:1; Rare:59 | ||||
| chr12:53299615-53299972 | Common:3; Rare:183 | ||||
| chr12:53321246-53321434 | Common:1; Rare:71; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53441497-53441787 | Common:1; Rare:80 | ||||
| chr12:53501213-53501352 | Rare:35 | ||||
| chr12:53626322-53626533 | Common:3; Rare:52 | ||||
| chr12:53676057-53676438 | Common:3; Rare:161 | ||||
| chr12:53727419-53727768 | Rare:79 | ||||
| chr12:53984740-53985275 | Common:5; Rare:116 | ||||
| chr12:53986235-53986286 | Rare:19 |