| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108731505-108731686 | Common:2; Rare:68 | ||||
| chr12:109021047-109021075 | Common:1; Rare:7 | ||||
| chr12:109052464-109052647 | Common:3; Rare:53 | ||||
| chr12:109093388-109093680 | Common:3; Rare:107 | ||||
| chr12:109097442-109097703 | Rare:92; Clinvar:3 | ||||
| chr12:109097896-109098250 | Common:5; Rare:110 | ||||
| chr12:109154331-109154651 | Rare:58 | ||||
| chr12:109477282-109477653 | Common:3; Rare:92 | ||||
| chr12:109573430-109573890 | Common:3; Rare:153; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr12:109900197-109900562 | Rare:107 | ||||
| chr12:109996220-109996445 | Common:2; Rare:67 | ||||
| chr12:109999087-109999203 | Rare:20 | ||||
| chr12:110403593-110403748 | Common:2; Rare:83 | ||||
| chr12:110403871-110404157 | Common:2; Rare:59 | ||||
| chr12:110468154-110468560 | Common:3; Rare:136 |