| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73385572-73385921 | Common:2; Rare:124; Clinvar:9; Clinvar (benign):3 | ||||
| chr2:73386024-73386185 | Rare:80; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr2:73386270-73386401 | Rare:44 | ||||
| chr2:73737123-73737634 | Common:4; Rare:166 | ||||
| chr2:73780002-73780291 | Common:2; Rare:114 | ||||
| chr2:73828783-73829107 | Common:2; Rare:77 | ||||
| chr2:73829183-73829438 | Common:5; Rare:67 | ||||
| chr2:73926675-73927344 | Common:2; Rare:236; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr2:73985844-73985922 | Common:1; Rare:14 | ||||
| chr2:74002561-74002803 | Common:2; Rare:86 | ||||
| chr2:74147600-74147733 | Rare:23 | ||||
| chr2:74147747-74148111 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:74178254-74178484 | Rare:49 | ||||
| chr2:74178717-74179103 | Common:6; Rare:118 | ||||
| chr2:74198341-74198789 | Rare:167 |