Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:19067414-19067715 | Common:5; Rare:124; Clinvar:1 | ||||
chr16:19522089-19522221 | Rare:33 | ||||
chr16:19555455-19555724 | Common:1; Rare:122 | ||||
chr16:19862006-19862126 | Rare:27 | ||||
chr16:20806349-20806533 | Rare:69 | ||||
chr16:21158563-21158659 | Common:1; Rare:27 | ||||
chr16:21952975-21953411 | Common:1; Rare:109; Clinvar (benign):3 | ||||
chr16:22436942-22437067 | Rare:46 | ||||
chr16:22437144-22437264 | Rare:38 | ||||
chr16:23453150-23453250 | Rare:27 | ||||
chr16:23557336-23557557 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr16:23641247-23641530 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24539323-24539584 | Common:1; Rare:84 | ||||
chr16:24729604-24729734 | Common:6; Rare:70 | ||||
chr16:25015370-25015457 | Common:2; Rare:29 |