| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112108985-112109186 | Rare:37 | ||||
| chr12:112109410-112109620 | Common:1; Rare:36 | ||||
| chr12:112125333-112125628 | Rare:75 | ||||
| chr12:112382080-112382176 | Rare:18 | ||||
| chr12:112382307-112382533 | Common:2; Rare:81 | ||||
| chr12:112409138-112409399 | Common:1; Rare:66 | ||||
| chr12:112409472-112409718 | Common:1; Rare:79 | ||||
| chr12:112418321-112418381 | Rare:16 | ||||
| chr12:112418397-112418664 | Rare:50 | ||||
| chr12:112418727-112419008 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:112419043-112419554 | Common:2; Rare:116; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:112419565-112419778 | Rare:38 | ||||
| chr12:112906831-112906898 | Rare:10 | ||||
| chr12:112906899-112907018 | Rare:26 | ||||
| chr12:112937991-112938051 | Rare:7 |