| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109996217-109996468 | Common:2; Rare:75 | ||||
| chr12:110281032-110281193 | Rare:63 | ||||
| chr12:110501559-110501724 | Common:1; Rare:57 | ||||
| chr12:110502058-110502195 | Common:1; Rare:51 | ||||
| chr12:111368982-111369249 | Common:1; Rare:69 | ||||
| chr12:111685769-111686168 | Rare:146 | ||||
| chr12:111766847-111767091 | Rare:78 | ||||
| chr12:111841894-111842254 | Common:3; Rare:100 | ||||
| chr12:111842467-111842692 | Common:1; Rare:52 | ||||
| chr12:112013086-112013566 | Common:1; Rare:177 | ||||
| chr12:113185345-113185824 | Common:10; Rare:183 | ||||
| chr12:113277415-113277464 | Common:2; Rare:9 | ||||
| chr12:114683879-114683908 | Rare:1 | ||||
| chr12:114683922-114684036 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr12:114684118-114684215 | Rare:32 |