| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109098293-109098533 | Rare:102; Clinvar:2 | ||||
| chr12:109154557-109154818 | Common:3; Rare:61 | ||||
| chr12:109477260-109477667 | Common:3; Rare:109 | ||||
| chr12:109573142-109573288 | Common:1; Rare:27 | ||||
| chr12:109573433-109573860 | Common:3; Rare:138; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880689 | Common:1; Rare:95 | ||||
| chr12:109899957-109900356 | Common:1; Rare:103 | ||||
| chr12:109996299-109996456 | Common:2; Rare:43 | ||||
| chr12:109999118-109999217 | Rare:15 | ||||
| chr12:109999467-109999638 | Rare:41 | ||||
| chr12:110067692-110067911 | Common:2; Rare:39 | ||||
| chr12:110280981-110281164 | Common:1; Rare:79 | ||||
| chr12:110403603-110403751 | Common:2; Rare:83 | ||||
| chr12:110468175-110468959 | Common:3; Rare:244 | ||||
| chr12:110502052-110502368 | Common:1; Rare:123 |