| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:53913484-53913783 | Common:1; Rare:56 | ||||
| chr2:53970009-53970195 | Rare:55 | ||||
| chr2:55282200-55282434 | Common:5; Rare:77 | ||||
| chr2:60100176-60100364 | Common:2; Rare:38 | ||||
| chr2:60557217-60557364 | Common:1; Rare:42 | ||||
| chr2:61492086-61492423 | Common:2; Rare:55; Clinvar (pathogenic):1 | ||||
| chr2:64525307-64525448 | Common:1; Rare:34 | ||||
| chr2:64946335-64946470 | Common:1; Rare:26 | ||||
| chr2:66583480-66583709 | Common:1; Rare:35 | ||||
| chr2:68352789-68352885 | Common:2; Rare:18 | ||||
| chr2:69798925-69799128 | Rare:30 | ||||
| chr2:69804547-69804682 | Common:1; Rare:49 | ||||
| chr2:70086250-70086476 | Common:4; Rare:92 | ||||
| chr2:70086483-70086785 | Common:2; Rare:131 | ||||
| chr2:74120210-74120364 | Rare:56 |