Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3305403-3305518 | Common:1; Rare:39 | ||||
chr16:3400967-3401224 | Common:6; Rare:94 | ||||
chr16:4425773-4425884 | Common:1; Rare:51 | ||||
chr16:4767146-4767330 | Common:1; Rare:57 | ||||
chr16:5071782-5071849 | Rare:30; Clinvar (benign):1 | ||||
chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr16:8868973-8869309 | Common:6; Rare:150 | ||||
chr16:10743750-10743880 | Rare:51 | ||||
chr16:11915883-11916208 | Common:2; Rare:134 | ||||
chr16:11976648-11976734 | Rare:28 | ||||
chr16:14071259-14071344 | Rare:27 | ||||
chr16:14630188-14630424 | Rare:102 | ||||
chr16:14632729-14632990 | Common:1; Rare:86 | ||||
chr16:15094247-15094409 | Rare:77 | ||||
chr16:15650061-15650280 | Common:1; Rare:109 |