Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:48244248-48244360 | Common:1; Rare:35 | ||||
chr16:53703821-53704167 | Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
chr16:56451312-56451600 | Common:1; Rare:91 | ||||
chr16:56682237-56682480 | Common:5; Rare:71 | ||||
chr16:56931915-56932147 | Common:2; Rare:110 | ||||
chr16:57186001-57186335 | Common:1; Rare:98 | ||||
chr16:57447360-57447493 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr16:66552476-66552701 | Rare:92 | ||||
chr16:66934363-66934460 | Common:1; Rare:41 | ||||
chr16:67227020-67227163 | Rare:56 | ||||
chr16:67393479-67393739 | Common:1; Rare:58 | ||||
chr16:67481108-67481404 | Common:1; Rare:104 | ||||
chr16:67660227-67660364 | Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67935662-67935896 | Common:1; Rare:66 | ||||
chr16:68023204-68023296 | Common:1; Rare:26 |