| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103965690-103965941 | Common:2; Rare:64 | ||||
| chr12:104064455-104064555 | Rare:27 | ||||
| chr12:104138147-104138392 | Common:1; Rare:62 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236078-105236265 | Common:2; Rare:89 | ||||
| chr12:106955635-106955923 | Rare:104 | ||||
| chr12:107685709-107685852 | Rare:49 | ||||
| chr12:107761092-107761273 | Common:3; Rare:70 | ||||
| chr12:108562399-108562664 | Common:8; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:109477287-109477650 | Common:3; Rare:89 | ||||
| chr12:109573423-109573837 | Common:4; Rare:137; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880381-109880664 | Common:1; Rare:86 | ||||
| chr12:109996299-109996439 | Common:2; Rare:39 | ||||
| chr12:110281032-110281212 | Rare:65 | ||||
| chr12:110403653-110403742 | Rare:54 |