| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2794864-2795226 | Common:1; Rare:126 | ||||
| chr12:2812507-2812727 | Common:1; Rare:56 | ||||
| chr12:2812880-2813017 | Rare:42 | ||||
| chr12:2877031-2877262 | Rare:70 | ||||
| chr12:3873317-3873514 | Common:2; Rare:43 | ||||
| chr12:4273513-4273810 | Rare:82 | ||||
| chr12:4320949-4321241 | Common:4; Rare:107 | ||||
| chr12:4538444-4538791 | Rare:72 | ||||
| chr12:4649010-4649149 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr12:6493240-6493370 | Common:5; Rare:37 | ||||
| chr12:6493843-6494119 | Common:2; Rare:82 | ||||
| chr12:6534642-6534841 | Common:3; Rare:77 | ||||
| chr12:6568260-6568382 | Rare:46 | ||||
| chr12:6607349-6607676 | Common:5; Rare:57 | ||||
| chr12:6688908-6689235 | Rare:103 |