| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112125328-112125649 | Rare:77 | ||||
| chr12:112125848-112125986 | Rare:19 | ||||
| chr12:112381808-112381943 | Rare:28 | ||||
| chr12:112382030-112382191 | Rare:23 | ||||
| chr12:112382203-112382556 | Common:2; Rare:112 | ||||
| chr12:112409138-112409293 | Common:1; Rare:35 | ||||
| chr12:112409302-112409373 | Rare:16 | ||||
| chr12:112409481-112409730 | Common:2; Rare:81 | ||||
| chr12:112418085-112418358 | Common:1; Rare:53 | ||||
| chr12:112418693-112419025 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:112419101-112419240 | Common:2; Rare:35; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:112419290-112419554 | Rare:61 | ||||
| chr12:112906831-112907034 | Rare:44 | ||||
| chr12:112916538-112916557 | Rare:5 | ||||
| chr12:112938250-112938650 | Common:5; Rare:98 |