| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218659587-218659767 | Rare:46 | ||||
| chr2:218671972-218672329 | Common:2; Rare:89 | ||||
| chr2:219176847-219177119 | Common:4; Rare:83 | ||||
| chr2:219178142-219178430 | Common:6; Rare:125 | ||||
| chr2:219206683-219206939 | Rare:91 | ||||
| chr2:219229303-219229477 | Rare:45 | ||||
| chr2:219229544-219229939 | Common:2; Rare:118 | ||||
| chr2:219245417-219245531 | Rare:33 | ||||
| chr2:219253859-219254056 | Common:1; Rare:62 | ||||
| chr2:219279203-219279523 | Common:2; Rare:100 | ||||
| chr2:219419854-219420155 | Common:2; Rare:62; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219420562-219420953 | Common:2; Rare:106; Clinvar:12; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr2:219498701-219498942 | Common:2; Rare:54 | ||||
| chr2:219597688-219597904 | Common:1; Rare:85 | ||||
| chr2:221572271-221572471 | Common:2; Rare:70 |