Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92848395-92848527 | Rare:51 | ||||
chr10:93702505-93702714 | Common:3; Rare:73 | ||||
chr10:95656657-95656761 | Rare:36; Clinvar:4 | ||||
chr10:95693856-95694219 | Common:5; Rare:121; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95907850-95907949 | Common:2; Rare:30 | ||||
chr10:96129986-96130053 | Rare:21 | ||||
chr10:96130219-96130523 | Common:1; Rare:103 | ||||
chr10:96832073-96832316 | Rare:94 | ||||
chr10:97334676-97334850 | Common:3; Rare:71 | ||||
chr10:97426032-97426291 | Common:3; Rare:108 | ||||
chr10:97445975-97446226 | Rare:66 | ||||
chr10:97498783-97499082 | Rare:91 | ||||
chr10:97687184-97687441 | Common:5; Rare:77 | ||||
chr10:97736994-97737198 | Common:1; Rare:68 | ||||
chr10:99430596-99430996 | Common:4; Rare:98 |