| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:48441527-48441560 | Rare:10 | ||||
| chr2:48755688-48755802 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr2:53767453-53768110 | Common:6; Rare:232 | ||||
| chr2:53768189-53768285 | Common:1; Rare:30 | ||||
| chr2:53768286-53768329 | Rare:7 | ||||
| chr2:53786812-53787102 | Rare:104 | ||||
| chr2:53970933-53971224 | Common:7; Rare:118 | ||||
| chr2:54115383-54115693 | Rare:101 | ||||
| chr2:54115698-54116027 | Common:6; Rare:137 | ||||
| chr2:54456143-54456370 | Rare:82 | ||||
| chr2:54457065-54457196 | Rare:57 | ||||
| chr2:54557802-54558044 | Rare:61 | ||||
| chr2:54558285-54558462 | Common:2; Rare:61 | ||||
| chr2:54558823-54559049 | Common:1; Rare:60 | ||||
| chr2:54723274-54723634 | Common:2; Rare:120 |