Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97426082-97426302 | Common:2; Rare:97 | ||||
chr10:97445975-97446252 | Rare:73 | ||||
chr10:97498694-97499040 | Common:2; Rare:99 | ||||
chr10:97687175-97687537 | Common:6; Rare:109 | ||||
chr10:98446885-98447021 | Rare:40 | ||||
chr10:99430601-99430936 | Common:3; Rare:77 | ||||
chr10:99659264-99659474 | Common:1; Rare:44 | ||||
chr10:99732076-99732312 | Rare:84; Clinvar:3 | ||||
chr10:100185938-100186132 | Rare:72 | ||||
chr10:100229547-100229631 | Rare:27 | ||||
chr10:100346973-100347438 | Common:3; Rare:103 | ||||
chr10:100529836-100529963 | Rare:37 | ||||
chr10:100535747-100535952 | Common:6; Rare:76 | ||||
chr10:100912637-100913050 | Common:1; Rare:119 | ||||
chr10:100987274-100987564 | Common:1; Rare:108; Clinvar (benign):1 |