| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55010221-55010250 | Rare:5 | ||||
| chr2:55049571-55049606 | Rare:16 | ||||
| chr2:55050261-55050463 | Common:1; Rare:74 | ||||
| chr2:55050469-55050803 | Common:3; Rare:100 | ||||
| chr2:55232067-55232386 | Common:4; Rare:72 | ||||
| chr2:55232574-55232760 | Common:1; Rare:74 | ||||
| chr2:55269122-55269458 | Common:3; Rare:80 | ||||
| chr2:55419295-55419351 | Rare:11 | ||||
| chr2:55419790-55420208 | Common:6; Rare:167 | ||||
| chr2:55519369-55519783 | Common:1; Rare:125 | ||||
| chr2:55616850-55617054 | Common:1; Rare:70 | ||||
| chr2:55617506-55617962 | Common:4; Rare:175 | ||||
| chr2:55693747-55693947 | Rare:83; Clinvar (benign):2 | ||||
| chr2:58046401-58047301 | Common:5; Rare:276 | ||||
| chr2:58047303-58047504 | Rare:57 |