Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68600464-68600689 | Rare:38 | ||||
chr10:68632316-68632353 | Common:2; Rare:9 | ||||
chr10:68672458-68672499 | Common:1; Rare:2 | ||||
chr10:68721778-68722032 | Common:1; Rare:48 | ||||
chr10:68756276-68756767 | Rare:80 | ||||
chr10:68778065-68778432 | Rare:76 | ||||
chr10:68952404-68952524 | Common:1; Rare:25 | ||||
chr10:68959558-68959877 | Rare:51 | ||||
chr10:68978832-68978853 | Rare:1 | ||||
chr10:69057345-69057632 | Common:2; Rare:64 | ||||
chr10:69061392-69061430 | Rare:3 | ||||
chr10:69086228-69086425 | Rare:34 | ||||
chr10:69088874-69089358 | Common:4; Rare:92 | ||||
chr10:69186357-69186475 | Rare:21 | ||||
chr10:69369232-69369625 | Common:1; Rare:91; Clinvar (benign):1 |