Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:98267926-98267943 | Rare:2 | ||||
chr10:98268145-98268433 | Common:2; Rare:75 | ||||
chr10:98446634-98446692 | Rare:7 | ||||
chr10:98446801-98446967 | Rare:42; Clinvar:1 | ||||
chr10:99430616-99431001 | Common:3; Rare:92 | ||||
chr10:99659245-99659565 | Common:1; Rare:81 | ||||
chr10:99732063-99732373 | Rare:116; Clinvar:5; Clinvar (benign):1 | ||||
chr10:100185920-100186198 | Rare:107 | ||||
chr10:100229516-100229631 | Rare:42 | ||||
chr10:100286631-100286763 | Common:3; Rare:70 | ||||
chr10:100346939-100347252 | Common:1; Rare:79 | ||||
chr10:100529831-100529968 | Rare:40 | ||||
chr10:100912741-100913050 | Common:1; Rare:95 | ||||
chr10:100913328-100913462 | Rare:34 | ||||
chr10:100969192-100969576 | Common:4; Rare:97 |