Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:7787938-7788263 | Common:1; Rare:133 | ||||
chr10:7818342-7818541 | Common:1; Rare:59 | ||||
chr10:11164741-11165594 | Common:3; Rare:195 | ||||
chr10:12043163-12043414 | Common:2; Rare:75 | ||||
chr10:12068649-12069051 | Common:2; Rare:142 | ||||
chr10:12129478-12129733 | Rare:105 | ||||
chr10:12195782-12195980 | Rare:48 | ||||
chr10:13099681-13099935 | Common:1; Rare:59 | ||||
chr10:13099967-13100302 | Common:4; Rare:84; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13116191-13116335 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr10:13300028-13300291 | Rare:81; Clinvar:1 | ||||
chr10:13302137-13302192 | Common:1; Rare:6 | ||||
chr10:13707547-13707653 | Rare:23 | ||||
chr10:13971819-13972109 | Common:2; Rare:60 | ||||
chr10:14008140-14008350 | Rare:52 |