| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54115423-54115496 | Rare:18 | ||||
| chr2:54115546-54115649 | Rare:34 | ||||
| chr2:55050302-55050818 | Common:5; Rare:167 | ||||
| chr2:55232234-55232870 | Common:6; Rare:199 | ||||
| chr2:55269176-55269421 | Common:3; Rare:61 | ||||
| chr2:55519403-55519814 | Common:1; Rare:127 | ||||
| chr2:58046471-58046553 | Rare:21 | ||||
| chr2:58046570-58046880 | Common:2; Rare:95 | ||||
| chr2:60881270-60881664 | Common:2; Rare:146 | ||||
| chr2:61017420-61017762 | Common:1; Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61065739-61065949 | Common:1; Rare:68 | ||||
| chr2:61144921-61145165 | Common:3; Rare:82 | ||||
| chr2:61177197-61177472 | Common:5; Rare:117 | ||||
| chr2:61470651-61470983 | Rare:112 | ||||
| chr2:61471224-61471387 | Common:2; Rare:58 |