Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:68539080-68539353 | Common:2; Rare:120 | ||||
chr16:69132547-69132671 | Rare:52 | ||||
chr16:69339548-69339821 | Common:1; Rare:110; Clinvar (benign):1 | ||||
chr16:69424489-69424695 | Common:1; Rare:60 | ||||
chr16:69726435-69726534 | Common:1; Rare:35 | ||||
chr16:69726537-69726737 | Common:3; Rare:45 | ||||
chr16:69754890-69755089 | Rare:80 | ||||
chr16:69762284-69762373 | Rare:20 | ||||
chr16:70114171-70114376 | Common:2; Rare:74 | ||||
chr16:70299132-70299205 | Rare:12 | ||||
chr16:70346804-70346952 | Common:1; Rare:74 | ||||
chr16:70523537-70523848 | Common:3; Rare:98 | ||||
chr16:71289353-71289468 | Rare:37 | ||||
chr16:71564926-71565021 | Rare:31 | ||||
chr16:71809031-71809308 | Common:3; Rare:90 |