| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69643611-69643853 | Rare:91 | ||||
| chr2:69829530-69829741 | Common:1; Rare:85 | ||||
| chr2:70257902-70258189 | Common:2; Rare:91 | ||||
| chr2:70293665-70293902 | Common:3; Rare:74 | ||||
| chr2:70301971-70302138 | Common:3; Rare:97 | ||||
| chr2:71068539-71068672 | Rare:59 | ||||
| chr2:71130224-71130677 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071701-73071841 | Common:2; Rare:54 | ||||
| chr2:73234173-73234353 | Common:1; Rare:51 | ||||
| chr2:73385644-73385860 | Common:2; Rare:85; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:73737300-73737582 | Common:3; Rare:93 | ||||
| chr2:73828804-73829037 | Common:1; Rare:54 | ||||
| chr2:73926696-73926934 | Common:2; Rare:114; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147866-74148062 | Common:1; Rare:53; Clinvar:2 | ||||
| chr2:74148272-74148449 | Common:1; Rare:39 |