Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:71895315-71895578 | Common:3; Rare:96 | ||||
chr16:72008544-72008760 | Common:2; Rare:67; Clinvar (benign):1 | ||||
chr16:72093587-72093963 | Rare:94 | ||||
chr16:74296442-74296882 | Common:1; Rare:135 | ||||
chr16:74666902-74667096 | Common:1; Rare:61 | ||||
chr16:75433336-75433852 | Common:4; Rare:171 | ||||
chr16:75556220-75556363 | Common:1; Rare:51; Clinvar (benign):3 | ||||
chr16:75623229-75623431 | Common:3; Rare:71 | ||||
chr16:75647635-75647837 | Common:2; Rare:95; Clinvar:3 | ||||
chr16:75648636-75648658 | Rare:12 | ||||
chr16:77191086-77191224 | Common:2; Rare:58 | ||||
chr16:79600732-79600947 | Common:1; Rare:62 | ||||
chr16:81006825-81007257 | Common:3; Rare:144 | ||||
chr16:81077203-81077353 | Common:1; Rare:71 | ||||
chr16:81314763-81315077 | Common:3; Rare:149; Clinvar:4; Clinvar (benign):1 |