Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:186806438-186806550 | Rare:35 | ||||
chr3:188153771-188153986 | Common:1; Rare:38 | ||||
chr3:188154060-188154215 | Rare:47 | ||||
chr3:190120362-190120561 | Rare:82; Clinvar (pathogenic):1 | ||||
chr3:190322426-190322530 | Rare:31 | ||||
chr3:193593101-193593372 | Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr3:196318163-196318340 | Common:1; Rare:77 | ||||
chr3:196503558-196503945 | Common:7; Rare:133 | ||||
chr3:196568527-196568652 | Common:2; Rare:31 | ||||
chr3:196942388-196942673 | Common:1; Rare:118 | ||||
chr3:197029779-197029917 | Common:1; Rare:45 | ||||
chr3:197298556-197298751 | Rare:64 | ||||
chr3:197736833-197737133 | Common:3; Rare:95 | ||||
chr3:197749753-197749984 | Common:1; Rare:86 | ||||
chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 |