Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100229553-100229664 | Rare:38 | ||||
chr10:100267601-100267757 | Common:3; Rare:49 | ||||
chr10:100286343-100286434 | Rare:21 | ||||
chr10:100286628-100286717 | Common:2; Rare:56 | ||||
chr10:100912770-100912981 | Common:1; Rare:59 | ||||
chr10:100987436-100987629 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr10:100999664-100999866 | Rare:60 | ||||
chr10:101031102-101031292 | Common:1; Rare:43 | ||||
chr10:101588125-101588327 | Rare:87 | ||||
chr10:101818352-101818762 | Common:1; Rare:109 | ||||
chr10:102120390-102120627 | Common:1; Rare:86 | ||||
chr10:102394344-102394597 | Common:1; Rare:68 | ||||
chr10:102395552-102395718 | Common:1; Rare:45 | ||||
chr10:102420792-102421286 | Common:1; Rare:151 | ||||
chr10:102644934-102645147 | Rare:42 |