Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:98446880-98447059 | Rare:51 | ||||
chr10:99430596-99430936 | Common:4; Rare:79 | ||||
chr10:99659264-99659539 | Common:1; Rare:67 | ||||
chr10:99732070-99732275 | Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100229583-100229652 | Rare:20 | ||||
chr10:100267616-100267746 | Common:2; Rare:40 | ||||
chr10:100286652-100286730 | Common:1; Rare:39 | ||||
chr10:100346519-100346626 | Common:2; Rare:24 | ||||
chr10:100346900-100347428 | Common:3; Rare:120 | ||||
chr10:100529836-100529972 | Rare:38 | ||||
chr10:100535701-100535952 | Common:6; Rare:87 | ||||
chr10:100912730-100912986 | Common:1; Rare:82 | ||||
chr10:100987228-100987571 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996974-100997132 | Common:1; Rare:42 | ||||
chr10:101588217-101588329 | Rare:47 |