| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61888215-61888449 | Rare:88 | ||||
| chr2:61888457-61888966 | Common:3; Rare:189 | ||||
| chr2:61905548-61905714 | Rare:69 | ||||
| chr2:62195943-62196227 | Common:3; Rare:99 | ||||
| chr2:62505766-62505936 | Common:2; Rare:59 | ||||
| chr2:62506131-62506341 | Common:1; Rare:81 | ||||
| chr2:62506344-62506418 | Rare:22 | ||||
| chr2:62705237-62705810 | Common:1; Rare:147 | ||||
| chr2:62705917-62705980 | Rare:18 | ||||
| chr2:62706148-62706314 | Rare:38 | ||||
| chr2:63050531-63050854 | Common:1; Rare:75 | ||||
| chr2:63587777-63588073 | Common:1; Rare:61 | ||||
| chr2:63588204-63589052 | Common:2; Rare:267; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:63840514-63840630 | Common:1; Rare:25 | ||||
| chr2:63840754-63841151 | Common:2; Rare:122 |