| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46073535-46073873 | Common:1; Rare:64 | ||||
| chr2:46617012-46617273 | Common:7; Rare:115 | ||||
| chr2:46915722-46915869 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916135 | Common:2; Rare:38 | ||||
| chr2:46941689-46941785 | Common:2; Rare:37; Clinvar (benign):1 | ||||
| chr2:47345005-47345148 | Common:1; Rare:36 | ||||
| chr2:47782950-47783157 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:48440626-48440777 | Common:3; Rare:62 | ||||
| chr2:53767559-53767891 | Common:5; Rare:121 | ||||
| chr2:53786848-53787191 | Common:1; Rare:131 | ||||
| chr2:53970780-53971141 | Common:11; Rare:125 | ||||
| chr2:54115581-54115693 | Rare:47 | ||||
| chr2:55050309-55050763 | Common:5; Rare:141 | ||||
| chr2:55232252-55232390 | Common:2; Rare:32 | ||||
| chr2:55519403-55519880 | Common:2; Rare:157 |