Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:46786780-46786899 | Rare:8 | ||||
chr10:47553478-47553545 | Rare:3 | ||||
chr10:47705941-47706046 | Common:3; Rare:27 | ||||
chr10:48720203-48720463 | Rare:62 | ||||
chr10:50622164-50622462 | Common:2; Rare:68 | ||||
chr10:50623372-50623468 | Common:1; Rare:20 | ||||
chr10:51696730-51696835 | Rare:11 | ||||
chr10:59695948-59696108 | Common:1; Rare:40 | ||||
chr10:61903016-61903366 | Common:1; Rare:91 | ||||
chr10:61988122-61988304 | Common:1; Rare:28 | ||||
chr10:62051169-62051293 | Rare:26 | ||||
chr10:63171907-63172162 | Common:1; Rare:54 | ||||
chr10:63184709-63185007 | Rare:74; Clinvar (benign):1 | ||||
chr10:63191092-63191273 | Rare:41 | ||||
chr10:63265158-63265321 | Rare:33 |