| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85595488-85595826 | Common:3; Rare:114 | ||||
| chr2:85602663-85602892 | Rare:57 | ||||
| chr2:85612024-85612129 | Rare:29 | ||||
| chr2:86105843-86106247 | Common:2; Rare:110 | ||||
| chr2:86195383-86195674 | Common:6; Rare:95 | ||||
| chr2:86199369-86199490 | Common:1; Rare:35 | ||||
| chr2:88691462-88691711 | Common:2; Rare:85 | ||||
| chr2:95165645-95165828 | Rare:58 | ||||
| chr2:95402594-95402757 | Rare:56 | ||||
| chr2:96208252-96208449 | Rare:96 | ||||
| chr2:96208816-96208942 | Common:3; Rare:42 | ||||
| chr2:96265968-96266348 | Common:2; Rare:114; Clinvar:1 | ||||
| chr2:96305449-96305638 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335697-96335812 | Common:1; Rare:39 | ||||
| chr2:97645808-97646097 | Common:2; Rare:89 |