Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:1056688-1056878 | Common:3; Rare:69 | ||||
chr10:3785127-3785554 | Common:4; Rare:163 | ||||
chr10:5813220-5813480 | Common:3; Rare:93 | ||||
chr10:6144688-6145008 | Common:2; Rare:82 | ||||
chr10:7787929-7788263 | Common:1; Rare:138 | ||||
chr10:7818396-7818526 | Common:1; Rare:30 | ||||
chr10:12068656-12069014 | Common:2; Rare:124 | ||||
chr10:12195790-12195984 | Rare:50 | ||||
chr10:13099941-13100302 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13300037-13300153 | Rare:46; Clinvar:1 | ||||
chr10:13707550-13707739 | Rare:44 | ||||
chr10:14838029-14838374 | Common:2; Rare:93 | ||||
chr10:14878655-14878909 | Common:2; Rare:73 | ||||
chr10:14953996-14954209 | Rare:75 | ||||
chr10:15097165-15097378 | Common:3; Rare:98 |