Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97426047-97426302 | Common:2; Rare:114 | ||||
chr10:97445955-97446239 | Common:1; Rare:79 | ||||
chr10:97498333-97498749 | Common:2; Rare:151 | ||||
chr10:97687266-97687595 | Common:3; Rare:101 | ||||
chr10:97737031-97737220 | Rare:68 | ||||
chr10:99430616-99430936 | Common:3; Rare:72 | ||||
chr10:99659231-99659571 | Common:2; Rare:89 | ||||
chr10:99732070-99732329 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185928-100186110 | Rare:73 | ||||
chr10:100267623-100267748 | Common:2; Rare:35 | ||||
chr10:100286603-100286725 | Common:4; Rare:74 | ||||
chr10:100346939-100347416 | Common:3; Rare:110 | ||||
chr10:100347422-100347454 | Rare:6 | ||||
chr10:100912629-100912998 | Common:1; Rare:106 | ||||
chr10:100913326-100913356 | Rare:10 |