| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108731456-108731688 | Common:2; Rare:85 | ||||
| chr12:109097847-109098250 | Common:5; Rare:126 | ||||
| chr12:109154557-109154843 | Common:3; Rare:66 | ||||
| chr12:109477275-109477653 | Common:3; Rare:96 | ||||
| chr12:109573430-109573813 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880662 | Common:1; Rare:90 | ||||
| chr12:110281024-110281270 | Rare:90 | ||||
| chr12:110450256-110450435 | Common:2; Rare:67 | ||||
| chr12:110468722-110468914 | Rare:53 | ||||
| chr12:110502058-110502218 | Common:1; Rare:58 | ||||
| chr12:110742655-110742705 | Common:1; Rare:10; Clinvar:1 | ||||
| chr12:111685761-111686110 | Rare:130 | ||||
| chr12:111766805-111767042 | Rare:75 | ||||
| chr12:111841877-111842241 | Common:3; Rare:100 | ||||
| chr12:112013123-112013498 | Common:1; Rare:139 |