| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200509918-200510008 | Common:1; Rare:31 | ||||
| chr2:200510032-200510162 | Rare:38 | ||||
| chr2:200811428-200811726 | Common:2; Rare:105 | ||||
| chr2:200811790-200812012 | Rare:90 | ||||
| chr2:200857713-200858079 | Rare:98 | ||||
| chr2:200864214-200864282 | Rare:28 | ||||
| chr2:200864559-200864747 | Common:1; Rare:61 | ||||
| chr2:200887771-200887952 | Common:2; Rare:38 | ||||
| chr2:200888986-200889516 | Common:3; Rare:162 | ||||
| chr2:200963532-200963887 | Common:1; Rare:94 | ||||
| chr2:201071592-201072047 | Rare:99 | ||||
| chr2:201115930-201116475 | Common:2; Rare:98 | ||||
| chr2:201118602-201118878 | Rare:42 | ||||
| chr2:201182581-201182866 | Common:1; Rare:63 | ||||
| chr2:201182996-201183147 | Common:1; Rare:21; Clinvar (benign):2 |