| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25982655-25982818 | Rare:37 | ||||
| chr2:26033436-26034245 | Common:5; Rare:267 | ||||
| chr2:26034347-26034425 | Rare:24 | ||||
| chr2:26034525-26034649 | Rare:46 | ||||
| chr2:26172974-26173195 | Rare:53 | ||||
| chr2:26184773-26185282 | Common:3; Rare:136 | ||||
| chr2:26185510-26185784 | Rare:51 | ||||
| chr2:26244584-26245031 | Common:2; Rare:155; Clinvar:6; Clinvar (benign):8 | ||||
| chr2:26245199-26245322 | Common:4; Rare:36 | ||||
| chr2:26245336-26245438 | Rare:27 | ||||
| chr2:26345147-26345369 | Common:1; Rare:32 | ||||
| chr2:26345515-26345635 | Common:1; Rare:25 | ||||
| chr2:26345670-26346227 | Common:2; Rare:162 | ||||
| chr2:26346233-26346285 | Rare:16 | ||||
| chr2:26346727-26346832 | Rare:20 |