| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218659338-218659759 | Common:4; Rare:102 | ||||
| chr2:218671977-218672339 | Common:2; Rare:89 | ||||
| chr2:218984497-218984586 | Rare:16 | ||||
| chr2:219176897-219177077 | Common:4; Rare:53 | ||||
| chr2:219177819-219177933 | Common:3; Rare:24 | ||||
| chr2:219178142-219178464 | Common:6; Rare:134 | ||||
| chr2:219206663-219206923 | Rare:93 | ||||
| chr2:219229586-219229891 | Common:1; Rare:90 | ||||
| chr2:219245407-219245526 | Rare:32 | ||||
| chr2:219253889-219254056 | Common:1; Rare:53 | ||||
| chr2:219279207-219279523 | Common:2; Rare:100 | ||||
| chr2:219419895-219420155 | Common:2; Rare:58; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219425657-219425883 | Rare:36; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr2:219441905-219442073 | Rare:38 | ||||
| chr2:219498701-219498928 | Common:2; Rare:47 |