| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74554535-74554757 | Common:1; Rare:77 | ||||
| chr2:74958529-74958707 | Common:4; Rare:67 | ||||
| chr2:74958872-74959081 | Rare:74 | ||||
| chr2:75710654-75710770 | Common:2; Rare:47 | ||||
| chr2:84459216-84459581 | Common:3; Rare:94; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905517-84905949 | Common:1; Rare:130 | ||||
| chr2:84970662-84970755 | Common:1; Rare:26 | ||||
| chr2:85327916-85328048 | Common:1; Rare:61 | ||||
| chr2:85354497-85354807 | Common:1; Rare:107 | ||||
| chr2:85410315-85410518 | Rare:52 | ||||
| chr2:85539107-85539363 | Common:3; Rare:134; Clinvar (benign):7 | ||||
| chr2:85561431-85561581 | Rare:56; Clinvar:4 | ||||
| chr2:85595555-85595849 | Common:2; Rare:102 | ||||
| chr2:85602345-85602472 | Rare:24 | ||||
| chr2:85602629-85602900 | Rare:70 |