Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153605124-153605372 | Rare:33 | ||||
chr1:153605517-153605582 | Rare:18 | ||||
chr1:153605928-153606141 | Rare:47 | ||||
chr1:153606584-153606663 | Rare:15 | ||||
chr1:153612037-153612065 | Rare:2 | ||||
chr1:153612141-153612323 | Common:1; Rare:37 | ||||
chr1:153654252-153654415 | Common:1; Rare:20 | ||||
chr1:153815752-153816034 | Common:3; Rare:58 | ||||
chr1:153835491-153835566 | Rare:12 | ||||
chr1:153995524-153995605 | Rare:8 | ||||
chr1:154275406-154275682 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
chr1:154726654-154726719 | Common:1; Rare:17 | ||||
chr1:154972909-154973186 | Common:1; Rare:58 | ||||
chr1:155003853-155004012 | Rare:37 | ||||
chr1:155052338-155052775 | Rare:106 |