| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:401433-401682 | Common:1; Rare:69 | ||||
| chr12:752368-752605 | Common:1; Rare:74 | ||||
| chr12:991093-991254 | Common:1; Rare:62 | ||||
| chr12:1592490-1592560 | Rare:13 | ||||
| chr12:1594551-1594854 | Common:1; Rare:88 | ||||
| chr12:1690736-1691180 | Common:4; Rare:143 | ||||
| chr12:2004431-2004669 | Common:2; Rare:72 | ||||
| chr12:2798717-2799223 | Common:1; Rare:126 | ||||
| chr12:2812488-2812732 | Common:1; Rare:62 | ||||
| chr12:2876974-2877279 | Rare:100 | ||||
| chr12:2959814-2959958 | Common:1; Rare:39 | ||||
| chr12:4320949-4321284 | Common:5; Rare:131 | ||||
| chr12:4538426-4538947 | Common:3; Rare:123 | ||||
| chr12:4649049-4649174 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr12:6341859-6342178 | Rare:67; Clinvar:1; Clinvar (benign):3 |