| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:110115677-110115998 | Common:4; Rare:78 | ||||
| chr2:110204935-110205062 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110678017-110678248 | Rare:73 | ||||
| chr2:111122436-111122744 | Common:3; Rare:128 | ||||
| chr2:111884039-111884235 | Common:1; Rare:49 | ||||
| chr2:112254977-112255152 | Common:1; Rare:74 | ||||
| chr2:112275417-112275642 | Common:1; Rare:69 | ||||
| chr2:112542109-112542493 | Common:1; Rare:118 | ||||
| chr2:112584378-112584639 | Common:1; Rare:71 | ||||
| chr2:112645696-112645948 | Common:1; Rare:93 | ||||
| chr2:112646253-112646378 | Common:1; Rare:44 | ||||
| chr2:112764584-112764815 | Common:2; Rare:77; Clinvar (pathogenic):1 | ||||
| chr2:112784452-112784770 | Rare:67 | ||||
| chr2:113117783-113118184 | Common:8; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:113236871-113236970 | Common:2; Rare:16 |