Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101037904-101038137 | Rare:29 | ||||
chr10:101588211-101588333 | Rare:49 | ||||
chr10:101694859-101694975 | Common:1; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
chr10:101817891-101817912 | Rare:8 | ||||
chr10:101818141-101818762 | Common:1; Rare:177 | ||||
chr10:102056089-102056366 | Common:1; Rare:67 | ||||
chr10:102114925-102115140 | Common:2; Rare:61 | ||||
chr10:102120437-102120565 | Common:1; Rare:50 | ||||
chr10:102152091-102152413 | Common:3; Rare:105 | ||||
chr10:102394337-102394582 | Common:1; Rare:65 | ||||
chr10:102502617-102502755 | Rare:50 | ||||
chr10:102644338-102644556 | Common:1; Rare:62 | ||||
chr10:102644736-102645131 | Rare:94 | ||||
chr10:102714271-102714631 | Common:2; Rare:120 | ||||
chr10:103094378-103094528 | Common:1; Rare:36 |