| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85665461-85665910 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:85665918-85665965 | Rare:5 | ||||
| chr2:85665999-85666897 | Common:17; Rare:264; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:85666901-85667032 | Rare:34 | ||||
| chr2:85705589-85705872 | Common:1; Rare:61 | ||||
| chr2:85709584-85709927 | Common:1; Rare:57 | ||||
| chr2:85711110-85711649 | Common:3; Rare:105 | ||||
| chr2:85713902-85714076 | Common:1; Rare:30 | ||||
| chr2:85779150-85779185 | Rare:5 | ||||
| chr2:85853882-85854144 | Common:3; Rare:43 | ||||
| chr2:85951609-85951896 | Common:3; Rare:59 | ||||
| chr2:86158605-86158887 | Common:4; Rare:59 | ||||
| chr2:86482369-86482580 | Rare:55 | ||||
| chr2:86500141-86500159 | Rare:2 | ||||
| chr2:86500573-86500606 | Rare:8 |