Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:55515126-55515356 | Common:3; Rare:38 | ||||
chr16:56498307-56498443 | Common:1; Rare:27; Clinvar (benign):1 | ||||
chr16:57184374-57184503 | Common:4; Rare:18 | ||||
chr16:57184918-57185107 | Rare:38 | ||||
chr16:57461230-57461528 | Common:1; Rare:56; Clinvar:2 | ||||
chr16:65069195-65069359 | Rare:35 | ||||
chr16:66803482-66803611 | Rare:24 | ||||
chr16:66954168-66954315 | Rare:28 | ||||
chr16:67229171-67229403 | Rare:46 | ||||
chr16:67263197-67263345 | Rare:25 | ||||
chr16:67390332-67390584 | Common:1; Rare:75 | ||||
chr16:68985941-68986132 | Rare:35 | ||||
chr16:69318705-69318890 | Common:1; Rare:82 | ||||
chr16:69566864-69566888 | Rare:3 | ||||
chr16:69711272-69711530 | Common:1; Rare:40 |