Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99235951-99236273 | Common:5; Rare:65 | ||||
chr10:99430622-99430986 | Common:3; Rare:88 | ||||
chr10:99659247-99659554 | Common:1; Rare:77 | ||||
chr10:99732070-99732349 | Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185920-100186198 | Rare:107 | ||||
chr10:100229516-100229657 | Rare:50 | ||||
chr10:100286660-100286763 | Common:2; Rare:46 | ||||
chr10:100912663-100913029 | Common:1; Rare:108 | ||||
chr10:100913338-100913436 | Rare:27 | ||||
chr10:100987270-100987577 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100999701-100999957 | Common:1; Rare:72 | ||||
chr10:101031111-101031292 | Common:1; Rare:40 | ||||
chr10:101588161-101588330 | Rare:70 | ||||
chr10:101818334-101818781 | Common:1; Rare:121 | ||||
chr10:102110602-102110893 | Rare:81 |