Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:129398108-129398310 | Common:1; Rare:29 | ||||
chr3:129399005-129399026 | Rare:4 | ||||
chr3:129452602-129452882 | Common:2; Rare:57 | ||||
chr3:129491842-129492095 | Common:2; Rare:53 | ||||
chr3:129606025-129606268 | Rare:49 | ||||
chr3:129723784-129723875 | Rare:14 | ||||
chr3:130111422-130111675 | Common:3; Rare:72 | ||||
chr3:130960595-130960729 | Common:1; Rare:18 | ||||
chr3:130991467-130991608 | Rare:26 | ||||
chr3:130992891-130993012 | Rare:20; Clinvar (benign):1 | ||||
chr3:132507086-132507354 | Common:1; Rare:62 | ||||
chr3:132667993-132668100 | Rare:18 | ||||
chr3:132718668-132718716 | Rare:7 | ||||
chr3:133586566-133586911 | Rare:87 | ||||
chr3:134196004-134196265 | Common:1; Rare:49 |