Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:62441848-62442158 | Common:2; Rare:62 | ||||
chr2:64453162-64453464 | Common:3; Rare:42 | ||||
chr2:64486128-64486354 | Common:2; Rare:50 | ||||
chr2:65018433-65018630 | Rare:50 | ||||
chr2:65567383-65567507 | Common:1; Rare:22 | ||||
chr2:69044490-69044802 | Rare:70; Clinvar (pathogenic):1 | ||||
chr2:69763337-69763503 | Rare:27 | ||||
chr2:69967064-69967260 | Rare:44 | ||||
chr2:70086246-70086485 | Common:4; Rare:93 | ||||
chr2:71050135-71050233 | Rare:23 | ||||
chr2:72027792-72027953 | Common:2; Rare:32 | ||||
chr2:72032792-72033040 | Rare:60 | ||||
chr2:72087235-72087515 | Common:2; Rare:79 | ||||
chr2:72144948-72145231 | Common:1; Rare:75 | ||||
chr2:72148910-72149218 | Rare:75 |