| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144520047-144520563 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020681-148021125 | Common:2; Rare:105; Clinvar (benign):2 | ||||
| chr2:149587307-149587366 | Rare:12 | ||||
| chr2:149587685-149587832 | Common:1; Rare:43; Clinvar:1 | ||||
| chr2:151828459-151828638 | Common:2; Rare:51 | ||||
| chr2:152175694-152176049 | Common:1; Rare:97 | ||||
| chr2:152717829-152717972 | Rare:61 | ||||
| chr2:153478644-153478953 | Common:2; Rare:84 | ||||
| chr2:156332677-156332870 | Rare:57; Clinvar:2 | ||||
| chr2:156436118-156436404 | Common:3; Rare:85 | ||||
| chr2:158456649-158456923 | Common:1; Rare:94 | ||||
| chr2:158968485-158968673 | Rare:58 | ||||
| chr2:159615216-159615343 | Common:2; Rare:29 | ||||
| chr2:159616434-159616609 | Common:2; Rare:35 | ||||
| chr2:159712345-159712584 | Common:2; Rare:91 |