| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88691462-88691696 | Common:2; Rare:76 | ||||
| chr2:95025581-95025733 | Rare:37 | ||||
| chr2:95165651-95165828 | Rare:54 | ||||
| chr2:95402600-95402757 | Rare:55 | ||||
| chr2:96208234-96208403 | Rare:92 | ||||
| chr2:96208816-96208879 | Common:2; Rare:23 | ||||
| chr2:96265984-96266343 | Common:2; Rare:106 | ||||
| chr2:96305475-96305618 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335697-96335779 | Common:1; Rare:27 | ||||
| chr2:98608445-98608636 | Common:1; Rare:84 | ||||
| chr2:99141554-99141768 | Common:2; Rare:67 | ||||
| chr2:99154933-99155037 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr2:99180979-99181227 | Common:2; Rare:72 | ||||
| chr2:100562732-100563070 | Common:3; Rare:111 | ||||
| chr2:101002183-101002320 | Rare:51 |