| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105330537-105330930 | Common:4; Rare:119 | ||||
| chr12:105353410-105353554 | Rare:32 | ||||
| chr12:106302566-106302866 | Common:6; Rare:78 | ||||
| chr12:106303131-106303197 | Rare:23 | ||||
| chr12:106357678-106357834 | Common:3; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357988-106358138 | Common:3; Rare:61 | ||||
| chr12:106601107-106601199 | Common:1; Rare:23 | ||||
| chr12:106684660-106684931 | Common:3; Rare:56 | ||||
| chr12:106774068-106774381 | Common:3; Rare:82 | ||||
| chr12:106774509-106774715 | Common:1; Rare:61 | ||||
| chr12:106955424-106955909 | Common:3; Rare:182 | ||||
| chr12:106987040-106987258 | Common:4; Rare:62 | ||||
| chr12:107092854-107093135 | Common:2; Rare:100 | ||||
| chr12:107093446-107093642 | Rare:68 | ||||
| chr12:107093791-107093958 | Common:2; Rare:44 |