Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2603353-2603472 | Rare:51 | ||||
chr16:2673362-2673705 | Common:10; Rare:122 | ||||
chr16:3022955-3023281 | Common:1; Rare:94 | ||||
chr16:15041066-15041310 | Common:1; Rare:70 | ||||
chr16:15704164-15704241 | Rare:24 | ||||
chr16:15708804-15708873 | Rare:37; Clinvar:8; Clinvar (benign):4 | ||||
chr16:15708893-15708986 | Rare:25 | ||||
chr16:15719218-15719459 | Common:1; Rare:75; Clinvar:6; Clinvar (benign):3 | ||||
chr16:15782370-15782684 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):7 | ||||
chr16:15784686-15784726 | Rare:15; Clinvar:2; Clinvar (benign):1 | ||||
chr16:15789078-15789163 | Rare:6 | ||||
chr16:15798658-15798715 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):4 | ||||
chr16:15854924-15855152 | Common:2; Rare:49 | ||||
chr16:17469194-17469377 | Rare:34 | ||||
chr16:21820398-21820433 | Rare:8 |