| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98608350-98608636 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:99154877-99155048 | Common:1; Rare:71; Clinvar (benign):2 | ||||
| chr2:99180978-99181233 | Common:2; Rare:72 | ||||
| chr2:99337315-99337585 | Rare:100 | ||||
| chr2:100322464-100322513 | Common:1; Rare:9 | ||||
| chr2:100417374-100417697 | Rare:97 | ||||
| chr2:101002162-101002314 | Rare:60 | ||||
| chr2:101252658-101252907 | Common:5; Rare:82 | ||||
| chr2:102736844-102736921 | Common:1; Rare:34 | ||||
| chr2:105037887-105038125 | Common:3; Rare:85 | ||||
| chr2:105337457-105337626 | Common:1; Rare:78 | ||||
| chr2:105438402-105438558 | Common:2; Rare:36 | ||||
| chr2:105438568-105438647 | Rare:21 | ||||
| chr2:106194222-106194568 | Common:6; Rare:150 | ||||
| chr2:108449097-108449242 | Rare:48 |