Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73811374-73812126 | Common:8; Rare:239 | ||||
chr10:73874459-73874813 | Rare:90 | ||||
chr10:73909149-73909450 | Common:2; Rare:41 | ||||
chr10:73910998-73911155 | Rare:47 | ||||
chr10:73997712-73998199 | Common:2; Rare:127; Clinvar (benign):1 | ||||
chr10:74150035-74150330 | Common:1; Rare:45 | ||||
chr10:74150360-74150385 | Rare:3 | ||||
chr10:74150522-74150618 | Rare:28 | ||||
chr10:74150680-74150853 | Common:3; Rare:31 | ||||
chr10:74151011-74151546 | Common:3; Rare:134 | ||||
chr10:74151552-74151784 | Common:2; Rare:44 | ||||
chr10:74176364-74176692 | Common:1; Rare:78; Clinvar:1 | ||||
chr10:74176703-74176818 | Rare:31; Clinvar:2 | ||||
chr10:74176823-74176956 | Common:1; Rare:48; Clinvar (benign):1 | ||||
chr10:74176959-74177283 | Common:1; Rare:60 |