| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88055732-88055935 | Rare:74 | ||||
| chr2:88127909-88128253 | Rare:80 | ||||
| chr2:88691440-88691853 | Common:2; Rare:160; Clinvar:1 | ||||
| chr2:95165649-95165828 | Rare:56 | ||||
| chr2:95207457-95207596 | Rare:56 | ||||
| chr2:95402607-95402880 | Rare:72 | ||||
| chr2:96208234-96208427 | Rare:100 | ||||
| chr2:96208724-96208908 | Common:4; Rare:68 | ||||
| chr2:96265959-96266386 | Common:2; Rare:126; Clinvar:1 | ||||
| chr2:96305475-96305638 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335719-96335822 | Common:1; Rare:35 | ||||
| chr2:97094848-97094966 | Common:1; Rare:22 | ||||
| chr2:97645879-97646189 | Common:3; Rare:94 | ||||
| chr2:97663892-97664261 | Common:1; Rare:115 | ||||
| chr2:98608374-98608665 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):1 |