Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93702380-93702723 | Common:5; Rare:110 | ||||
chr10:93893915-93894044 | Rare:55 | ||||
chr10:94362897-94363054 | Common:3; Rare:64 | ||||
chr10:94545686-94545892 | Common:4; Rare:71 | ||||
chr10:95561334-95561576 | Common:3; Rare:66 | ||||
chr10:95656613-95656761 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):2 | ||||
chr10:95656791-95656900 | Rare:23 | ||||
chr10:95693891-95694081 | Common:2; Rare:69; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:95907746-95907967 | Common:3; Rare:67 | ||||
chr10:96043382-96043583 | Common:1; Rare:82 | ||||
chr10:96129695-96129803 | Rare:22 | ||||
chr10:96129924-96130068 | Common:1; Rare:52 | ||||
chr10:96130229-96130461 | Common:1; Rare:84 | ||||
chr10:96130470-96130584 | Rare:32 | ||||
chr10:96831970-96832305 | Rare:130 |