| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568733-218568939 | Common:1; Rare:53 | ||||
| chr2:218659606-218659767 | Rare:43 | ||||
| chr2:218671977-218672078 | Rare:34 | ||||
| chr2:219176922-219177068 | Common:4; Rare:45 | ||||
| chr2:219178142-219178383 | Common:6; Rare:113 | ||||
| chr2:219180953-219181162 | Rare:58 | ||||
| chr2:219206683-219206916 | Rare:86 | ||||
| chr2:219229577-219229891 | Common:2; Rare:95 | ||||
| chr2:219245424-219245516 | Rare:26 | ||||
| chr2:219279203-219279545 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:219418588-219418941 | Common:2; Rare:112; Clinvar:25; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:219419856-219420155 | Common:2; Rare:62; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219460611-219460867 | Common:3; Rare:58 | ||||
| chr2:219498663-219498928 | Common:2; Rare:56 | ||||
| chr2:221572271-221572522 | Common:6; Rare:89 |