| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:48529242-48529376 | Common:1; Rare:38 | ||||
| chr2:53767491-53767871 | Common:5; Rare:121 | ||||
| chr2:53786842-53787207 | Common:1; Rare:141 | ||||
| chr2:53970762-53971177 | Common:12; Rare:154 | ||||
| chr2:54115560-54115682 | Rare:50 | ||||
| chr2:55050282-55050790 | Common:5; Rare:164 | ||||
| chr2:55232245-55232877 | Common:5; Rare:202 | ||||
| chr2:55519452-55519913 | Common:2; Rare:149 | ||||
| chr2:55618849-55618870 | Rare:5 | ||||
| chr2:58046609-58046885 | Common:2; Rare:85 | ||||
| chr2:60550899-60551005 | Rare:30 | ||||
| chr2:60553569-60553888 | Rare:50 | ||||
| chr2:60881322-60881781 | Common:3; Rare:157 | ||||
| chr2:61017117-61017756 | Common:5; Rare:189; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144901-61145165 | Common:3; Rare:90 |