| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25878282-25878642 | Common:1; Rare:99 | ||||
| chr2:26033739-26034151 | Common:4; Rare:155 | ||||
| chr2:26244545-26244990 | Common:2; Rare:162; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345758-26346165 | Common:2; Rare:123 | ||||
| chr2:26764191-26764325 | Common:1; Rare:52 | ||||
| chr2:27032862-27032970 | Rare:37 | ||||
| chr2:27051544-27051727 | Rare:57 | ||||
| chr2:27071730-27072024 | Common:1; Rare:77 | ||||
| chr2:27211775-27212065 | Common:3; Rare:104 | ||||
| chr2:27212223-27212387 | Common:2; Rare:88 | ||||
| chr2:27217215-27217483 | Rare:105 | ||||
| chr2:27323058-27323149 | Rare:23 | ||||
| chr2:27356743-27356855 | Rare:29 | ||||
| chr2:27356973-27357170 | Common:2; Rare:67 | ||||
| chr2:27370267-27370641 | Common:1; Rare:155 |