| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104138147-104138371 | Rare:53 | ||||
| chr12:104986208-104986364 | Common:2; Rare:56 | ||||
| chr12:105107615-105107803 | Common:1; Rare:90; Clinvar:1 | ||||
| chr12:105176060-105176192 | Rare:45 | ||||
| chr12:105236068-105236271 | Common:2; Rare:94 | ||||
| chr12:105330537-105330924 | Common:4; Rare:118 | ||||
| chr12:107685709-107685945 | Rare:77 | ||||
| chr12:108339297-108339553 | Common:2; Rare:64 | ||||
| chr12:108531205-108531476 | Rare:63 | ||||
| chr12:108561120-108561463 | Common:4; Rare:92 | ||||
| chr12:108562396-108562695 | Common:9; Rare:125; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633879-108634058 | Rare:32 | ||||
| chr12:109052545-109052632 | Common:1; Rare:22 | ||||
| chr12:109154541-109154691 | Common:1; Rare:39 | ||||
| chr12:109477287-109477653 | Common:3; Rare:90 |