| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12725625-12725942 | Common:4; Rare:73 | ||||
| chr12:12891271-12891567 | Common:1; Rare:60 | ||||
| chr12:13000190-13000447 | Common:1; Rare:84 | ||||
| chr12:14365482-14365743 | Common:1; Rare:88 | ||||
| chr12:14567712-14567976 | Common:1; Rare:54 | ||||
| chr12:14771123-14771257 | Rare:43 | ||||
| chr12:14774184-14774752 | Common:3; Rare:172 | ||||
| chr12:14803451-14803699 | Common:1; Rare:64 | ||||
| chr12:14884718-14884781 | Rare:8 | ||||
| chr12:14885727-14885980 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:14961538-14961863 | Common:3; Rare:81 | ||||
| chr12:15221231-15221540 | Common:1; Rare:86 | ||||
| chr12:15221555-15221574 | Rare:7 | ||||
| chr12:15882272-15882626 | Common:1; Rare:109 | ||||
| chr12:16347480-16347756 | Common:5; Rare:51 |