Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:129183783-129184075 | Common:2; Rare:99 | ||||
chr3:129249561-129249675 | Common:1; Rare:34 | ||||
chr3:129316282-129316315 | Rare:17 | ||||
chr3:129439819-129440335 | Common:1; Rare:158; Clinvar:2; Clinvar (benign):1 | ||||
chr3:129893545-129893875 | Rare:130 | ||||
chr3:130746766-130746934 | Common:3; Rare:52 | ||||
chr3:130893914-130894231 | Common:3; Rare:92 | ||||
chr3:131026749-131026940 | Common:2; Rare:50 | ||||
chr3:131381451-131381801 | Common:3; Rare:87 | ||||
chr3:132417319-132417544 | Common:2; Rare:62 | ||||
chr3:132659785-132659937 | Common:3; Rare:36 | ||||
chr3:132722137-132722237 | Common:1; Rare:44; Clinvar:5; Clinvar (benign):2 | ||||
chr3:133661856-133662015 | Rare:37 | ||||
chr3:134485442-134485773 | Rare:82 | ||||
chr3:134485950-134486208 | Common:3; Rare:90 |