| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218659603-218659777 | Rare:48 | ||||
| chr2:218671977-218672363 | Common:2; Rare:97 | ||||
| chr2:219176926-219177098 | Common:4; Rare:55 | ||||
| chr2:219178149-219178355 | Common:6; Rare:110 | ||||
| chr2:219206683-219206929 | Rare:90 | ||||
| chr2:219229336-219229360 | Rare:5 | ||||
| chr2:219229582-219229875 | Common:2; Rare:78 | ||||
| chr2:219245407-219245511 | Rare:26 | ||||
| chr2:219279203-219279535 | Common:2; Rare:105 | ||||
| chr2:219418619-219419035 | Common:2; Rare:140; Clinvar:32; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr2:219419881-219420166 | Common:2; Rare:66; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219460602-219460871 | Common:3; Rare:63 | ||||
| chr2:219498670-219498928 | Common:2; Rare:54 | ||||
| chr2:221572271-221572490 | Common:3; Rare:76 | ||||
| chr2:221573963-221574214 | Common:2; Rare:45 |