| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108731456-108731688 | Common:2; Rare:85 | ||||
| chr12:109052466-109052644 | Common:3; Rare:49 | ||||
| chr12:109093607-109093903 | Common:2; Rare:67 | ||||
| chr12:109097848-109098239 | Common:5; Rare:125 | ||||
| chr12:109477272-109477667 | Common:3; Rare:104 | ||||
| chr12:109573435-109573845 | Common:3; Rare:133; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880668 | Common:1; Rare:91 | ||||
| chr12:109900209-109900332 | Rare:54 | ||||
| chr12:109999071-109999231 | Rare:30 | ||||
| chr12:110450235-110450437 | Common:2; Rare:75 | ||||
| chr12:110468716-110468914 | Rare:53 | ||||
| chr12:110502051-110502195 | Common:1; Rare:53 | ||||
| chr12:111685754-111686085 | Rare:124 | ||||
| chr12:111841894-111842225 | Common:3; Rare:90 | ||||
| chr12:112013129-112013467 | Common:1; Rare:119 |