| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110468671-110468915 | Rare:61 | ||||
| chr12:110502058-110502195 | Common:1; Rare:51 | ||||
| chr12:111685737-111686114 | Rare:136 | ||||
| chr12:111766769-111766992 | Rare:68 | ||||
| chr12:111841867-111842225 | Common:3; Rare:99 | ||||
| chr12:112013129-112013472 | Common:1; Rare:120 | ||||
| chr12:112108755-112108845 | Rare:28 | ||||
| chr12:112409528-112409707 | Common:1; Rare:62 | ||||
| chr12:113185435-113185785 | Common:8; Rare:124 | ||||
| chr12:113966312-113966540 | Common:9; Rare:78 | ||||
| chr12:114406035-114406329 | Common:1; Rare:66 | ||||
| chr12:114407915-114408356 | Common:2; Rare:86; Clinvar (benign):5 | ||||
| chr12:114408644-114409014 | Rare:76 | ||||
| chr12:114683891-114684353 | Common:4; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:114684460-114684683 | Common:1; Rare:66 |