Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:14632729-14632981 | Common:1; Rare:84 | ||||
chr16:15094247-15094389 | Rare:71 | ||||
chr16:15643048-15643273 | Rare:76 | ||||
chr16:18801588-18801890 | Common:2; Rare:85 | ||||
chr16:20806433-20806610 | Rare:61 | ||||
chr16:21953026-21953386 | Common:1; Rare:83 | ||||
chr16:23557336-23557473 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641229-23641530 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):3 | ||||
chr16:25111537-25111796 | Common:2; Rare:67 | ||||
chr16:27268719-27268850 | Common:1; Rare:41 | ||||
chr16:27313614-27313989 | Common:8; Rare:99 | ||||
chr16:27549886-27550161 | Common:2; Rare:98 | ||||
chr16:28822573-28822729 | Rare:56 | ||||
chr16:28846257-28846623 | Common:2; Rare:126; Clinvar:6; Clinvar (benign):6 | ||||
chr16:28879887-28880046 | Common:3; Rare:48 |