| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568784-218568966 | Common:1; Rare:57 | ||||
| chr2:218659594-218659743 | Rare:35 | ||||
| chr2:218671977-218672334 | Common:2; Rare:89 | ||||
| chr2:219160785-219160922 | Common:1; Rare:38 | ||||
| chr2:219176897-219177114 | Common:4; Rare:65 | ||||
| chr2:219178136-219178406 | Common:6; Rare:118 | ||||
| chr2:219206704-219206916 | Rare:78 | ||||
| chr2:219229313-219229419 | Rare:34 | ||||
| chr2:219229541-219229912 | Common:2; Rare:117 | ||||
| chr2:219245407-219245526 | Rare:32 | ||||
| chr2:219253870-219254056 | Common:1; Rare:58 | ||||
| chr2:219279217-219279523 | Common:2; Rare:97 | ||||
| chr2:219418405-219419045 | Common:5; Rare:214; Clinvar:40; Clinvar (benign):22; Clinvar (pathogenic):3 | ||||
| chr2:219419881-219420673 | Common:6; Rare:225; Clinvar:24; Clinvar (benign):25; Clinvar (pathogenic):4 | ||||
| chr2:219425483-219425776 | Common:1; Rare:49; Clinvar:4; Clinvar (pathogenic):2 |