Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28924654-28925077 | Common:3; Rare:130 | ||||
chr16:28925140-28925968 | Common:2; Rare:207 | ||||
chr16:28931818-28932102 | Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr16:28932686-28933047 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
chr16:28950572-28951068 | Common:2; Rare:146 | ||||
chr16:28951323-28951485 | Common:1; Rare:48 | ||||
chr16:28974501-28974870 | Common:2; Rare:133 | ||||
chr16:28984717-28984787 | Rare:15 | ||||
chr16:28984949-28985161 | Common:1; Rare:65 | ||||
chr16:29662732-29662987 | Common:3; Rare:36 | ||||
chr16:29663114-29663334 | Rare:46 | ||||
chr16:29678979-29679224 | Rare:73 | ||||
chr16:29679554-29679756 | Common:2; Rare:42 | ||||
chr16:29745939-29746255 | Common:2; Rare:62 | ||||
chr16:29790396-29790838 | Common:2; Rare:153; Clinvar (benign):2 |