Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:3577331-3577534 | Common:3; Rare:53 | ||||
chr16:3577705-3577712 | |||||
chr16:3611454-3611922 | Common:1; Rare:180; Clinvar:2 | ||||
chr16:3717268-3717863 | Common:1; Rare:225; Clinvar:1; Clinvar (benign):1 | ||||
chr16:3879979-3880362 | Common:2; Rare:128 | ||||
chr16:3880638-3880973 | Common:4; Rare:111 | ||||
chr16:4116412-4116719 | Common:2; Rare:113 | ||||
chr16:4272317-4272416 | Rare:20 | ||||
chr16:4272513-4272631 | Rare:38 | ||||
chr16:4272845-4273059 | Common:1; Rare:39 | ||||
chr16:4273506-4273542 | Rare:7 | ||||
chr16:4314726-4315047 | Common:1; Rare:67 | ||||
chr16:4351220-4351545 | Common:2; Rare:142 | ||||
chr16:4371612-4371916 | Common:1; Rare:108 | ||||
chr16:4415884-4415945 | Rare:19 |