| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178601818-178601921 | Rare:26; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:178615285-178615789 | Common:1; Rare:132; Clinvar:27; Clinvar (benign):8 | ||||
| chr2:178617118-178617631 | Common:3; Rare:130; Clinvar:18; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr2:178618182-178618735 | Common:1; Rare:132; Clinvar:18; Clinvar (benign):7 | ||||
| chr2:178618741-178618996 | Rare:63; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:178620713-178621369 | Common:2; Rare:167; Clinvar:14; Clinvar (benign):11 | ||||
| chr2:178629359-178629750 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:178631182-178631505 | Rare:63; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:178632524-178633045 | Common:1; Rare:141; Clinvar:19; Clinvar (benign):6 | ||||
| chr2:178643401-178643697 | Common:1; Rare:34 | ||||
| chr2:178649082-178649145 | Rare:14 | ||||
| chr2:178668856-178669165 | Common:2; Rare:49 | ||||
| chr2:178671100-178671251 | Rare:44; Clinvar:5; Clinvar (benign):4 | ||||
| chr2:178674295-178674493 | Rare:43; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:178683019-178683461 | Common:2; Rare:69; Clinvar:6; Clinvar (benign):2 |