| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58046619-58046845 | Rare:68 | ||||
| chr2:58047014-58047136 | Rare:34 | ||||
| chr2:58047224-58047296 | Rare:23 | ||||
| chr2:60881387-60881720 | Common:3; Rare:109 | ||||
| chr2:61017092-61017205 | Common:1; Rare:34 | ||||
| chr2:61017425-61017760 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61065739-61065977 | Common:1; Rare:77 | ||||
| chr2:61144926-61145165 | Common:3; Rare:79 | ||||
| chr2:61177299-61177495 | Common:3; Rare:86 | ||||
| chr2:61186001-61186405 | Common:1; Rare:110 | ||||
| chr2:61471245-61471387 | Common:2; Rare:52 | ||||
| chr2:61888529-61888693 | Common:1; Rare:70 | ||||
| chr2:63588718-63589043 | Rare:101 | ||||
| chr2:63840791-63841185 | Common:3; Rare:115 | ||||
| chr2:63841614-63842201 | Common:4; Rare:176 |