| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210562669-210562963 | Common:3; Rare:54 | ||||
| chr2:210573294-210573483 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:215772788-215772826 | Rare:9 | ||||
| chr2:215773324-215773411 | Rare:13 | ||||
| chr2:215830419-215830583 | Rare:32 | ||||
| chr2:218402636-218402714 | Rare:24 | ||||
| chr2:218964163-218964308 | Common:1; Rare:15 | ||||
| chr2:219200861-219201165 | Common:1; Rare:84 | ||||
| chr2:219685024-219685299 | Common:2; Rare:78 | ||||
| chr2:222843022-222843176 | Rare:24 | ||||
| chr2:223026415-223026638 | Common:2; Rare:37 | ||||
| chr2:223042865-223042991 | Common:3; Rare:29 | ||||
| chr2:223724044-223724306 | Common:5; Rare:39 | ||||
| chr2:223725662-223725779 | Common:3; Rare:18 | ||||
| chr2:223975679-223976099 | Common:3; Rare:79 |