| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108334120-108334500 | Common:3; Rare:81 | ||||
| chr12:108335149-108335744 | Common:7; Rare:124 | ||||
| chr12:108335904-108336304 | Common:2; Rare:82 | ||||
| chr12:108337202-108337540 | Rare:51 | ||||
| chr12:108337764-108338186 | Common:4; Rare:120 | ||||
| chr12:108360420-108361148 | Common:4; Rare:177 | ||||
| chr12:108511940-108512250 | Common:1; Rare:64 | ||||
| chr12:108517797-108518439 | Common:4; Rare:246 | ||||
| chr12:108541084-108541575 | Common:2; Rare:210 | ||||
| chr12:108559623-108560064 | Common:10; Rare:137 | ||||
| chr12:108560214-108560614 | Common:3; Rare:112 | ||||
| chr12:108563467-108563867 | Common:7; Rare:178 | ||||
| chr12:108566015-108566990 | Common:8; Rare:421 | ||||
| chr12:108568874-108568991 | Rare:25; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:108569318-108569964 | Common:6; Rare:199 |