Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100286623-100286738 | Common:3; Rare:68 | ||||
chr10:100346928-100347543 | Common:5; Rare:147 | ||||
chr10:100912741-100913039 | Common:1; Rare:94 | ||||
chr10:100969232-100969570 | Common:3; Rare:86 | ||||
chr10:100987156-100987621 | Common:2; Rare:162; Clinvar:1; Clinvar (benign):2 | ||||
chr10:101588140-101588348 | Rare:86; Clinvar:1 | ||||
chr10:101694558-101694780 | Common:4; Rare:57; Clinvar:4; Clinvar (benign):5 | ||||
chr10:101818294-101818762 | Common:1; Rare:131 | ||||
chr10:102056089-102056368 | Common:1; Rare:67 | ||||
chr10:102152029-102152483 | Common:4; Rare:149 | ||||
chr10:102394335-102394570 | Rare:64 | ||||
chr10:102395553-102395735 | Common:1; Rare:51 | ||||
chr10:102432543-102432703 | Common:1; Rare:41 | ||||
chr10:102461384-102461435 | Rare:11 | ||||
chr10:102644985-102645142 | Rare:36 |