Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3443452-3443729 | Common:3; Rare:92 | ||||
chr16:3717509-3717627 | Rare:61 | ||||
chr16:4425767-4425881 | Common:1; Rare:52 | ||||
chr16:8797612-8797925 | Common:1; Rare:127; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr16:19067593-19067667 | Common:2; Rare:43 | ||||
chr16:20806445-20806641 | Rare:64 | ||||
chr16:21953033-21953413 | Common:1; Rare:97; Clinvar (benign):3 | ||||
chr16:23641295-23641533 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
chr16:25015323-25015461 | Common:2; Rare:48 | ||||
chr16:27549894-27550158 | Common:2; Rare:92 | ||||
chr16:28846270-28846626 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28925165-28925370 | Rare:63 | ||||
chr16:29805343-29805710 | Common:2; Rare:173 | ||||
chr16:29807945-29808155 | Rare:124 | ||||
chr16:29996070-29996259 | Common:2; Rare:65 |