Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4476270-4476483 | Common:3; Rare:80 | ||||
chr16:4538740-4538877 | Rare:57 | ||||
chr16:4614886-4615027 | Common:1; Rare:37 | ||||
chr16:4767160-4767321 | Common:1; Rare:47 | ||||
chr16:5071791-5071861 | Rare:35; Clinvar (benign):1 | ||||
chr16:8621625-8621703 | Common:1; Rare:31 | ||||
chr16:8797618-8797866 | Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
chr16:8868983-8869212 | Common:3; Rare:108 | ||||
chr16:10580573-10580741 | Rare:54 | ||||
chr16:10944327-10944582 | Common:1; Rare:75 | ||||
chr16:11851500-11851635 | Rare:66 | ||||
chr16:11915895-11916227 | Common:2; Rare:134 | ||||
chr16:11976624-11976760 | Common:2; Rare:48 | ||||
chr16:14071065-14071350 | Common:1; Rare:96 | ||||
chr16:14630195-14630383 | Rare:88 |