Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4767134-4767330 | Common:1; Rare:65 | ||||
chr16:4847261-4847441 | Common:1; Rare:76 | ||||
chr16:5097741-5098004 | Common:4; Rare:94 | ||||
chr16:8797624-8797877 | Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr16:10580581-10580854 | Common:2; Rare:93 | ||||
chr16:11851511-11851635 | Rare:61 | ||||
chr16:11915889-11916215 | Common:2; Rare:134 | ||||
chr16:11976628-11976766 | Rare:51 | ||||
chr16:14630195-14630397 | Rare:92 | ||||
chr16:14632715-14632990 | Common:1; Rare:95 | ||||
chr16:15094247-15094446 | Rare:93 | ||||
chr16:15650076-15650280 | Common:1; Rare:103 | ||||
chr16:15856992-15857151 | Common:2; Rare:37; Clinvar (benign):2 | ||||
chr16:19067422-19067702 | Common:5; Rare:114; Clinvar:1 | ||||
chr16:19067796-19067917 | Common:2; Rare:29 |