Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10430158-10430548 | Common:7; Rare:95 | ||||
chr1:10430651-10430799 | Common:5; Rare:49 | ||||
chr1:10431206-10431305 | Rare:21 | ||||
chr1:10472417-10472701 | Rare:70 | ||||
chr1:10474847-10475035 | Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11012244-11012432 | Rare:45 | ||||
chr1:11012607-11012742 | Common:1; Rare:44; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11013048-11013142 | Rare:34 | ||||
chr1:11055737-11055835 | Rare:24 | ||||
chr1:11059271-11059612 | Common:1; Rare:88 | ||||
chr1:11059932-11060283 | Common:2; Rare:108 | ||||
chr1:11262496-11262839 | Common:2; Rare:100 | ||||
chr1:11272903-11273238 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273461-11273519 | Common:1; Rare:23; Clinvar (benign):1 | ||||
chr1:11654314-11655062 | Common:5; Rare:188 |