| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95991527-95991617 | Rare:25 | ||||
| chr2:95991753-95992002 | Common:1; Rare:54 | ||||
| chr2:96145438-96145742 | Common:3; Rare:71 | ||||
| chr2:96208225-96208467 | Rare:124 | ||||
| chr2:96208781-96208954 | Common:3; Rare:71 | ||||
| chr2:96265911-96266356 | Common:2; Rare:134; Clinvar:3 | ||||
| chr2:96305391-96305662 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96325269-96325330 | Rare:18 | ||||
| chr2:96335712-96335813 | Common:1; Rare:34 | ||||
| chr2:96537189-96537314 | Rare:22 | ||||
| chr2:96638276-96638448 | Common:1; Rare:43 | ||||
| chr2:96740039-96740348 | Common:5; Rare:70 | ||||
| chr2:96816000-96816283 | Common:4; Rare:104 | ||||
| chr2:96866543-96866824 | Rare:79 | ||||
| chr2:96868519-96868778 | Rare:67 |