Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:95656647-95656977 | Rare:90; Clinvar:5 | ||||
chr10:95907835-95907914 | Rare:20 | ||||
chr10:96831986-96832299 | Rare:121 | ||||
chr10:97426056-97426302 | Common:2; Rare:107 | ||||
chr10:97445983-97446229 | Rare:63 | ||||
chr10:97498382-97498569 | Common:2; Rare:72 | ||||
chr10:97498694-97498985 | Common:2; Rare:86 | ||||
chr10:98134555-98134688 | Common:1; Rare:43 | ||||
chr10:98446856-98446963 | Rare:27 | ||||
chr10:99430622-99430944 | Common:3; Rare:73 | ||||
chr10:99659258-99659529 | Common:1; Rare:67 | ||||
chr10:99732070-99732339 | Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185895-100186182 | Rare:108 | ||||
chr10:100346921-100347252 | Common:1; Rare:82 | ||||
chr10:100912770-100912998 | Common:1; Rare:66 |