Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:53208359-53208496 | Rare:30 | ||||
chr16:53703821-53704194 | Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
chr16:56451280-56451615 | Common:1; Rare:109 | ||||
chr16:56608228-56608748 | Common:4; Rare:146 | ||||
chr16:56625616-56625845 | Rare:72 | ||||
chr16:56729967-56730202 | Common:1; Rare:54 | ||||
chr16:56931885-56932148 | Common:2; Rare:119 | ||||
chr16:57185962-57186382 | Common:1; Rare:128 | ||||
chr16:57244956-57245370 | Common:3; Rare:142 | ||||
chr16:57447360-57447514 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr16:57984864-57985163 | Common:3; Rare:75 | ||||
chr16:58129295-58129570 | Common:2; Rare:87 | ||||
chr16:58515449-58515534 | Rare:40 | ||||
chr16:65122019-65122196 | Common:1; Rare:59 | ||||
chr16:66552446-66552668 | Rare:97 |