| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218400928-218401205 | Common:7; Rare:80 | ||||
| chr2:218568301-218568647 | Common:3; Rare:94 | ||||
| chr2:218568733-218568972 | Common:1; Rare:67 | ||||
| chr2:218659339-218659363 | Rare:8 | ||||
| chr2:218659600-218659755 | Rare:40 | ||||
| chr2:218662648-218662935 | Rare:72; Clinvar (pathogenic):3 | ||||
| chr2:218671967-218672334 | Common:2; Rare:93 | ||||
| chr2:218782023-218782327 | Rare:94; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219125633-219125838 | Rare:30 | ||||
| chr2:219176897-219177041 | Common:3; Rare:41 | ||||
| chr2:219177819-219177933 | Common:3; Rare:24 | ||||
| chr2:219206681-219206923 | Rare:87 | ||||
| chr2:219229544-219229896 | Common:2; Rare:111 | ||||
| chr2:219245391-219245531 | Rare:40 | ||||
| chr2:219279207-219279527 | Common:2; Rare:101 |