Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:55395833-55395994 | Common:1; Rare:47; Clinvar:2 | ||||
chr4:55546798-55546987 | Common:2; Rare:64 | ||||
chr4:56387417-56387528 | Rare:35 | ||||
chr4:56435474-56435753 | Common:5; Rare:104 | ||||
chr4:56435975-56436315 | Rare:119 | ||||
chr4:56467527-56467708 | Common:2; Rare:74; Clinvar (benign):5 | ||||
chr4:56977570-56977771 | Common:1; Rare:77 | ||||
chr4:57109877-57110180 | Rare:105 | ||||
chr4:57110349-57110536 | Common:1; Rare:61 | ||||
chr4:67545427-67545742 | Common:2; Rare:77 | ||||
chr4:67701117-67701404 | Common:4; Rare:133 | ||||
chr4:70688153-70688594 | Common:2; Rare:112 | ||||
chr4:70704600-70704810 | Common:1; Rare:66 | ||||
chr4:70839232-70839389 | Common:2; Rare:59 | ||||
chr4:70902206-70902478 | Common:5; Rare:97 |