| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200889059-200889439 | Common:3; Rare:121 | ||||
| chr2:200963634-200963936 | Common:1; Rare:73 | ||||
| chr2:201071626-201072048 | Rare:86 | ||||
| chr2:201642659-201642748 | Rare:49 | ||||
| chr2:202238510-202238681 | Common:1; Rare:62 | ||||
| chr2:202911881-202912202 | Common:1; Rare:79 | ||||
| chr2:206159384-206159672 | Common:2; Rare:96 | ||||
| chr2:206765324-206765621 | Common:2; Rare:71; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:207529747-207530015 | Common:3; Rare:88 | ||||
| chr2:218217057-218217226 | Common:1; Rare:62 | ||||
| chr2:218270109-218270418 | Common:5; Rare:93 | ||||
| chr2:218292480-218292614 | Rare:37 | ||||
| chr2:218568307-218568584 | Common:2; Rare:71 | ||||
| chr2:218568733-218568939 | Common:1; Rare:53 | ||||
| chr2:218659603-218659733 | Rare:31 |