Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:91410185-91410498 | Common:4; Rare:116 | ||||
chr10:92291036-92291317 | Common:3; Rare:83 | ||||
chr10:92574027-92574110 | Common:1; Rare:23 | ||||
chr10:92592952-92593187 | Common:3; Rare:68 | ||||
chr10:92848344-92848530 | Rare:72 | ||||
chr10:93702478-93702709 | Common:4; Rare:86 | ||||
chr10:93757695-93758059 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr10:94362901-94363046 | Common:2; Rare:61 | ||||
chr10:94545714-94545837 | Common:2; Rare:39 | ||||
chr10:95561334-95561541 | Common:3; Rare:53 | ||||
chr10:95693877-95694207 | Common:5; Rare:107; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95907842-95907916 | Rare:19 | ||||
chr10:96271516-96271780 | Rare:47 | ||||
chr10:96831983-96832302 | Rare:123 | ||||
chr10:97426044-97426297 | Common:2; Rare:109 |