Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:10743722-10743869 | Rare:60 | ||||
chr16:11851517-11851635 | Rare:57 | ||||
chr16:11976628-11976766 | Rare:51 | ||||
chr16:15094238-15094415 | Common:1; Rare:84 | ||||
chr16:20806435-20806659 | Rare:71 | ||||
chr16:22436942-22437067 | Rare:46 | ||||
chr16:23557343-23557594 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641278-23641530 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
chr16:25111529-25111792 | Common:2; Rare:70 | ||||
chr16:27268719-27268872 | Common:1; Rare:52 | ||||
chr16:27549865-27550161 | Common:2; Rare:112 | ||||
chr16:28553887-28554009 | Common:3; Rare:42 | ||||
chr16:28846299-28846675 | Common:2; Rare:120; Clinvar:5; Clinvar (benign):3 | ||||
chr16:29995610-29995698 | Rare:42 | ||||
chr16:29996083-29996252 | Common:2; Rare:57 |