Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:72008551-72008772 | Common:2; Rare:73; Clinvar (benign):1 | ||||
chr16:72013908-72014081 | Common:1; Rare:34 | ||||
chr16:72014313-72014530 | Common:1; Rare:57 | ||||
chr16:72093538-72093957 | Rare:108 | ||||
chr16:73047932-73048074 | Rare:34 | ||||
chr16:73048584-73048822 | Common:1; Rare:57 | ||||
chr16:73059037-73059103 | Rare:4 | ||||
chr16:74296460-74296938 | Common:1; Rare:160 | ||||
chr16:74304174-74304393 | Common:2; Rare:46 | ||||
chr16:74607011-74607194 | Rare:100 | ||||
chr16:74666828-74667071 | Common:4; Rare:94 | ||||
chr16:74701095-74701323 | Common:2; Rare:44 | ||||
chr16:74985013-74985291 | Common:2; Rare:95 | ||||
chr16:75433288-75433818 | Common:4; Rare:176 | ||||
chr16:75464342-75464445 | Common:4; Rare:43 |