| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88055679-88055804 | Rare:47 | ||||
| chr2:88691462-88691732 | Common:2; Rare:98 | ||||
| chr2:95121771-95122084 | Rare:100 | ||||
| chr2:95165651-95165828 | Rare:54 | ||||
| chr2:95207425-95207590 | Rare:69 | ||||
| chr2:95402436-95402757 | Rare:97 | ||||
| chr2:96208242-96208427 | Rare:94 | ||||
| chr2:96208805-96208979 | Common:3; Rare:67 | ||||
| chr2:96265959-96266348 | Common:2; Rare:118; Clinvar:1 | ||||
| chr2:96305475-96305608 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335719-96335801 | Common:1; Rare:26 | ||||
| chr2:96857932-96858239 | Common:2; Rare:109 | ||||
| chr2:96870810-96870934 | Rare:28 | ||||
| chr2:97094835-97094972 | Common:1; Rare:29 | ||||
| chr2:97663919-97664261 | Common:1; Rare:105 |