| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88691418-88691846 | Common:3; Rare:167; Clinvar:1 | ||||
| chr2:95121727-95121923 | Common:1; Rare:81 | ||||
| chr2:95165396-95165464 | Rare:8 | ||||
| chr2:95165651-95165828 | Rare:54 | ||||
| chr2:95207457-95207599 | Rare:57 | ||||
| chr2:95402594-95402767 | Rare:58 | ||||
| chr2:96208293-96208492 | Rare:90 | ||||
| chr2:96208761-96208801 | Common:1; Rare:19 | ||||
| chr2:96208804-96208879 | Common:2; Rare:32 | ||||
| chr2:96265946-96266489 | Common:2; Rare:151; Clinvar:2 | ||||
| chr2:96278285-96278578 | Rare:73; Clinvar:1 | ||||
| chr2:96278654-96278857 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr2:96305376-96305652 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335697-96335842 | Common:2; Rare:52 | ||||
| chr2:96816015-96816277 | Common:3; Rare:99 |