| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12891278-12891567 | Common:1; Rare:58 | ||||
| chr12:13000183-13000486 | Common:2; Rare:94 | ||||
| chr12:14365482-14365719 | Common:1; Rare:77 | ||||
| chr12:14567687-14567976 | Common:2; Rare:60 | ||||
| chr12:14774184-14774589 | Common:3; Rare:117 | ||||
| chr12:14803409-14803670 | Common:2; Rare:66 | ||||
| chr12:14885715-14885980 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:15221267-15221547 | Common:1; Rare:78 | ||||
| chr12:15789444-15789755 | Rare:85 | ||||
| chr12:15882263-15882431 | Rare:67 | ||||
| chr12:16347453-16347724 | Common:4; Rare:50 | ||||
| chr12:16605018-16605126 | Rare:26 | ||||
| chr12:16605947-16606012 | Rare:18 | ||||
| chr12:16606318-16606916 | Rare:137 | ||||
| chr12:20369558-20369830 | Common:2; Rare:116 |