Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:57447360-57447508 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
chr16:66934365-66934451 | Rare:37 | ||||
chr16:67109802-67109989 | Rare:59 | ||||
chr16:67227020-67227158 | Rare:54 | ||||
chr16:67481093-67481372 | Common:1; Rare:105 | ||||
chr16:67660222-67660366 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67719307-67719441 | Rare:34 | ||||
chr16:68023209-68023296 | Common:1; Rare:22 | ||||
chr16:68264443-68264564 | Rare:43 | ||||
chr16:68310934-68311056 | Common:1; Rare:62 | ||||
chr16:69132547-69132672 | Rare:52 | ||||
chr16:69339565-69339799 | Rare:90; Clinvar (benign):1 | ||||
chr16:69424478-69424678 | Rare:57 | ||||
chr16:69726443-69726868 | Common:3; Rare:111 | ||||
chr16:69762284-69762367 | Rare:19 |