Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97736930-97737191 | Common:2; Rare:89 | ||||
chr10:98134561-98134688 | Common:1; Rare:41 | ||||
chr10:98446870-98446977 | Rare:29 | ||||
chr10:99430626-99430923 | Common:3; Rare:68 | ||||
chr10:99659247-99659529 | Common:1; Rare:72 | ||||
chr10:99732072-99732331 | Rare:95; Clinvar:4 | ||||
chr10:100185955-100186190 | Rare:90 | ||||
chr10:100229553-100229689 | Rare:49 | ||||
chr10:100286343-100286735 | Common:5; Rare:143 | ||||
chr10:100346939-100347397 | Common:1; Rare:104 | ||||
chr10:100912759-100913005 | Common:1; Rare:72 | ||||
chr10:100913324-100913367 | Rare:16 | ||||
chr10:100987265-100987599 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031102-101031292 | Common:1; Rare:43 | ||||
chr10:101588174-101588339 | Rare:70 |