Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97445981-97446229 | Rare:64 | ||||
chr10:97713281-97713455 | Rare:27 | ||||
chr10:97714378-97714701 | Common:1; Rare:85 | ||||
chr10:97736994-97737227 | Common:1; Rare:78 | ||||
chr10:99430616-99430959 | Common:3; Rare:83 | ||||
chr10:99659265-99659536 | Common:1; Rare:66 | ||||
chr10:99732072-99732331 | Rare:95; Clinvar:4 | ||||
chr10:100185885-100186203 | Rare:114 | ||||
chr10:100912751-100913023 | Common:1; Rare:84 | ||||
chr10:100987439-100987613 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr10:101031111-101031494 | Common:1; Rare:87 | ||||
chr10:101588180-101588338 | Rare:65 | ||||
chr10:101817983-101818224 | Rare:81 | ||||
chr10:102056100-102056324 | Common:1; Rare:55 | ||||
chr10:102394291-102394582 | Common:1; Rare:78 |