| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:111884156-111884255 | Rare:27 | ||||
| chr2:112055459-112055608 | Common:2; Rare:42 | ||||
| chr2:112255012-112255277 | Common:2; Rare:92 | ||||
| chr2:112275404-112275642 | Common:1; Rare:78 | ||||
| chr2:112481975-112482326 | Common:3; Rare:124 | ||||
| chr2:112542119-112542504 | Common:2; Rare:121 | ||||
| chr2:112584346-112584647 | Common:1; Rare:85 | ||||
| chr2:112645707-112645955 | Common:1; Rare:93 | ||||
| chr2:112764596-112764773 | Common:1; Rare:54 | ||||
| chr2:113157260-113157486 | Common:3; Rare:55 | ||||
| chr2:113198829-113198983 | Rare:58 | ||||
| chr2:113235449-113235744 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:113236909-113236937 | Common:1 | ||||
| chr2:113236948-113236978 | Rare:6 | ||||
| chr2:113437567-113437874 | Common:2; Rare:102 |