| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017429-61017762 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144916-61145184 | Common:3; Rare:87 | ||||
| chr2:61177309-61177481 | Common:3; Rare:77 | ||||
| chr2:61470667-61470996 | Rare:109 | ||||
| chr2:61471257-61471393 | Common:4; Rare:50 | ||||
| chr2:61538219-61538442 | Common:1; Rare:53 | ||||
| chr2:61538490-61538810 | Common:1; Rare:81 | ||||
| chr2:61853981-61854207 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888460-61888700 | Common:1; Rare:106 | ||||
| chr2:62506146-62506324 | Common:1; Rare:70 | ||||
| chr2:63588236-63588566 | Common:1; Rare:99; Clinvar:6 | ||||
| chr2:63588618-63589025 | Common:1; Rare:123; Clinvar (benign):1 | ||||
| chr2:63840800-63841182 | Common:3; Rare:110 | ||||
| chr2:63841673-63841955 | Common:1; Rare:98 | ||||
| chr2:64144314-64144683 | Common:4; Rare:107 |