| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086938-70087116 | Rare:88 | ||||
| chr2:70087686-70087941 | Rare:86 | ||||
| chr2:70087943-70088428 | Common:1; Rare:130 | ||||
| chr2:70258002-70258242 | Common:2; Rare:86 | ||||
| chr2:70293645-70293844 | Common:2; Rare:69 | ||||
| chr2:71068538-71068654 | Rare:53 | ||||
| chr2:71130200-71130668 | Common:6; Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453441-71453912 | Common:3; Rare:86 | ||||
| chr2:72144502-72144684 | Common:2; Rare:39 | ||||
| chr2:73737300-73737484 | Common:2; Rare:58 | ||||
| chr2:73828804-73829012 | Common:1; Rare:49 | ||||
| chr2:74147849-74148052 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74198407-74198643 | Rare:91 | ||||
| chr2:74421629-74421759 | Rare:42 | ||||
| chr2:74440429-74440677 | Rare:68 |