| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218217049-218217226 | Common:1; Rare:65 | ||||
| chr2:218270096-218270557 | Common:5; Rare:144; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:218287255-218287382 | Rare:22 | ||||
| chr2:218568301-218568908 | Common:5; Rare:150 | ||||
| chr2:218659605-218659743 | Rare:33 | ||||
| chr2:218671977-218672061 | Rare:29 | ||||
| chr2:219176926-219177067 | Common:4; Rare:43 | ||||
| chr2:219206716-219206923 | Rare:73 | ||||
| chr2:219229581-219229873 | Common:2; Rare:78 | ||||
| chr2:219245407-219245511 | Rare:26 | ||||
| chr2:219419895-219420165 | Common:2; Rare:61; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219498691-219498928 | Common:2; Rare:50 | ||||
| chr2:223957257-223957482 | Common:4; Rare:84 | ||||
| chr2:226835952-226836113 | Common:1; Rare:62 | ||||
| chr2:227325191-227325341 | Common:4; Rare:52 |