| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102120065-102120256 | Rare:75 | ||||
| chr12:103587117-103587285 | Rare:42 | ||||
| chr12:103930033-103930563 | Common:9; Rare:178 | ||||
| chr12:103943605-103943869 | Rare:52 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064435-104064606 | Rare:42 | ||||
| chr12:104138147-104138422 | Common:1; Rare:78 | ||||
| chr12:105107621-105107795 | Common:1; Rare:80 | ||||
| chr12:105236084-105236331 | Common:2; Rare:117 | ||||
| chr12:106357759-106357825 | Common:2; Rare:16; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:106955509-106955917 | Common:1; Rare:151 | ||||
| chr12:106956661-106956825 | Rare:28 | ||||
| chr12:106987049-106987277 | Common:4; Rare:67 | ||||
| chr12:108562439-108562699 | Common:9; Rare:112; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108730185-108730425 | Common:1; Rare:46 |