| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99141147-99141441 | Common:1; Rare:104 | ||||
| chr2:99141528-99141725 | Common:2; Rare:72 | ||||
| chr2:99154877-99155055 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr2:99180967-99181234 | Common:2; Rare:79 | ||||
| chr2:99337220-99337512 | Rare:100 | ||||
| chr2:99389528-99389777 | Common:1; Rare:46 | ||||
| chr2:99396634-99396884 | Rare:62 | ||||
| chr2:99489946-99490258 | Common:1; Rare:135 | ||||
| chr2:100417363-100417675 | Rare:94 | ||||
| chr2:100562606-100563054 | Common:5; Rare:128 | ||||
| chr2:100820999-100821155 | Common:2; Rare:38 | ||||
| chr2:101002156-101002318 | Rare:63 | ||||
| chr2:101109948-101110154 | Common:2; Rare:38 | ||||
| chr2:101151594-101151684 | Common:3; Rare:26 | ||||
| chr2:101252646-101252907 | Common:5; Rare:88 |