| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102120065-102120254 | Rare:74 | ||||
| chr12:103930044-103930564 | Common:8; Rare:176 | ||||
| chr12:103965705-103965971 | Common:2; Rare:58 | ||||
| chr12:104064048-104064199 | Rare:32 | ||||
| chr12:104064228-104064614 | Common:2; Rare:91 | ||||
| chr12:104287204-104287430 | Rare:59 | ||||
| chr12:104288789-104288936 | Rare:72 | ||||
| chr12:105107615-105107789 | Common:1; Rare:79 | ||||
| chr12:105236040-105236296 | Common:2; Rare:112 | ||||
| chr12:106357810-106357813 | |||||
| chr12:107685709-107685925 | Rare:73 | ||||
| chr12:108562394-108562700 | Common:9; Rare:126; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109098357-109098539 | Rare:79; Clinvar:2 | ||||
| chr12:109477272-109477667 | Common:3; Rare:104 | ||||
| chr12:109573485-109573813 | Common:3; Rare:93; Clinvar:3; Clinvar (benign):5 |