| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534332-6534582 | Common:5; Rare:109 | ||||
| chr12:6534642-6534860 | Common:3; Rare:87 | ||||
| chr12:6556038-6556243 | Common:3; Rare:73 | ||||
| chr12:6568249-6568359 | Rare:39 | ||||
| chr12:6688843-6689245 | Rare:119 | ||||
| chr12:6689454-6689732 | Common:2; Rare:70 | ||||
| chr12:6723852-6724289 | Common:1; Rare:94 | ||||
| chr12:6752937-6753189 | Common:6; Rare:77 | ||||
| chr12:6851922-6852180 | Rare:66 | ||||
| chr12:6867381-6867619 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868587-6868896 | Common:2; Rare:76; Clinvar (pathogenic):1 | ||||
| chr12:6868903-6869158 | Rare:75; Clinvar:2 | ||||
| chr12:6873291-6873541 | Common:1; Rare:73 | ||||
| chr12:6927930-6928293 | Common:1; Rare:76 | ||||
| chr12:6943531-6943817 | Common:4; Rare:116 |