Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27628983-27629077 | Common:1; Rare:49 | ||||
chr2:27663386-27663434 | Rare:13 | ||||
chr2:27663607-27663911 | Rare:108 | ||||
chr2:27771634-27771792 | Common:1; Rare:59 | ||||
chr2:28751726-28752116 | Common:1; Rare:165 | ||||
chr2:28870278-28870429 | Rare:52 | ||||
chr2:32039761-32039844 | Rare:26 | ||||
chr2:32165752-32165895 | Common:1; Rare:51 | ||||
chr2:37084328-37084561 | Common:3; Rare:90 | ||||
chr2:37231563-37231696 | Common:4; Rare:72; Clinvar (benign):3 | ||||
chr2:37324724-37324954 | Common:1; Rare:94 | ||||
chr2:37671599-37671895 | Common:11; Rare:120 | ||||
chr2:39437115-39437429 | Common:4; Rare:108 | ||||
chr2:44361767-44361986 | Common:1; Rare:65 | ||||
chr2:46617037-46617263 | Common:7; Rare:95 |