Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:56519774-56519814 | Rare:16; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr16:56564950-56565147 | Common:1; Rare:49 | ||||
chr16:56625642-56625833 | Rare:56 | ||||
chr16:56729977-56730205 | Common:1; Rare:52 | ||||
chr16:56989371-56989594 | Common:1; Rare:52; Clinvar:1 | ||||
chr16:57186001-57186339 | Common:1; Rare:101 | ||||
chr16:57447354-57447514 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
chr16:57619975-57620116 | Rare:33 | ||||
chr16:57797865-57798244 | Rare:128 | ||||
chr16:58515423-58515534 | Common:1; Rare:45 | ||||
chr16:66552386-66552660 | Rare:107 | ||||
chr16:66934360-66934506 | Common:1; Rare:53 | ||||
chr16:66988466-66988754 | Common:1; Rare:58 | ||||
chr16:67028989-67029105 | Rare:39 | ||||
chr16:67159885-67160012 | Rare:20 |