| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55419778-55420186 | Common:5; Rare:163 | ||||
| chr2:55519404-55519804 | Common:1; Rare:124 | ||||
| chr2:55618841-55618924 | Rare:24 | ||||
| chr2:55693781-55693993 | Common:1; Rare:73; Clinvar (benign):2 | ||||
| chr2:58241294-58241471 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:60550882-60551005 | Rare:31 | ||||
| chr2:60881290-60881681 | Common:2; Rare:142 | ||||
| chr2:61017148-61017762 | Common:5; Rare:181; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144887-61145176 | Common:3; Rare:96 | ||||
| chr2:61177173-61177472 | Common:6; Rare:121 | ||||
| chr2:61470661-61471000 | Rare:112 | ||||
| chr2:61471224-61471387 | Common:2; Rare:58 | ||||
| chr2:61536714-61536795 | Rare:22 | ||||
| chr2:61537568-61537866 | Common:2; Rare:87 | ||||
| chr2:61538186-61538390 | Common:1; Rare:47 |