Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100912184-100912428 | Rare:53 | ||||
chr10:100912609-100913045 | Common:1; Rare:121 | ||||
chr10:100913282-100913461 | Common:1; Rare:56 | ||||
chr10:100987203-100987616 | Common:2; Rare:148; Clinvar:1; Clinvar (benign):2 | ||||
chr10:100996490-100996591 | Rare:18 | ||||
chr10:100996958-100997290 | Common:2; Rare:84 | ||||
chr10:100997513-100997941 | Common:3; Rare:86 | ||||
chr10:100999173-100999368 | Common:3; Rare:33 | ||||
chr10:100999610-100999732 | Common:1; Rare:31 | ||||
chr10:101031102-101031311 | Common:1; Rare:46 | ||||
chr10:101061088-101061562 | Common:1; Rare:117 | ||||
chr10:101062542-101062848 | Common:3; Rare:110 | ||||
chr10:101066645-101066795 | Common:2; Rare:32 | ||||
chr10:101353753-101354246 | Common:1; Rare:148 | ||||
chr10:101354521-101354607 | Rare:23 |