| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176637582-176637754 | Common:3; Rare:60 | ||||
| chr2:177215465-177215891 | Common:2; Rare:97 | ||||
| chr2:178592564-178593084 | Common:1; Rare:144; Clinvar:21; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr2:178599423-178599573 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:178602114-178602432 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:178607801-178608365 | Common:4; Rare:155; Clinvar:25; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr2:178615452-178615510 | Rare:17; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:178632973-178633150 | Rare:63; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:178646506-178646619 | Rare:24; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:178688675-178689056 | Common:2; Rare:100; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:181123906-181123957 | Rare:11 | ||||
| chr2:186499893-186500293 | Common:2; Rare:73 | ||||
| chr2:187467003-187467187 | Common:1; Rare:47 | ||||
| chr2:187539455-187539558 | Common:1; Rare:14 | ||||
| chr2:188990111-188990381 | Rare:78; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):5 |