| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12611785-12612135 | Common:3; Rare:95 | ||||
| chr12:12696160-12696292 | Rare:37 | ||||
| chr12:12696677-12696741 | Rare:27 | ||||
| chr12:12714762-12714895 | Rare:36 | ||||
| chr12:12717528-12717883 | Common:2; Rare:114; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr12:12725649-12725843 | Common:2; Rare:48 | ||||
| chr12:12979742-12979881 | Rare:13 | ||||
| chr12:13000098-13000481 | Common:2; Rare:120 | ||||
| chr12:13044353-13044436 | Rare:26 | ||||
| chr12:13103542-13103784 | Rare:48 | ||||
| chr12:14365455-14365782 | Common:1; Rare:106 | ||||
| chr12:14385241-14385385 | Rare:27 | ||||
| chr12:14567677-14567937 | Common:2; Rare:56 | ||||
| chr12:14771112-14771157 | Rare:31 | ||||
| chr12:14774184-14774752 | Common:3; Rare:172 |