Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:50217715-50217925 | Rare:110; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr22:50274902-50274991 | Common:4; Rare:19 | ||||
chr22:50526961-50527035 | Rare:21 | ||||
chr3:1906004-1906057 | Rare:12 | ||||
chr3:3135268-3135582 | Common:6; Rare:64 | ||||
chr3:3152930-3153176 | Rare:51 | ||||
chr3:3858197-3858313 | Rare:20 | ||||
chr3:4318801-4318855 | Common:3; Rare:12 | ||||
chr3:8177268-8177335 | Rare:19 | ||||
chr3:8191776-8191986 | Common:7; Rare:39 | ||||
chr3:9390273-9390494 | Rare:54 | ||||
chr3:9398473-9398602 | Rare:31 | ||||
chr3:9398741-9398879 | Rare:46 | ||||
chr3:9453755-9454044 | Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr3:9914907-9915204 | Common:1; Rare:56 |