Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:1048874-1049079 | Common:2; Rare:111 | ||||
chr10:3785121-3785551 | Common:4; Rare:162 | ||||
chr10:6202769-6202946 | Common:4; Rare:46 | ||||
chr10:7787929-7788254 | Common:1; Rare:137 | ||||
chr10:7818401-7818541 | Common:1; Rare:32 | ||||
chr10:12195770-12196286 | Rare:148 | ||||
chr10:13099952-13100302 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13161297-13161591 | Common:1; Rare:77 | ||||
chr10:13348006-13348351 | Rare:112 | ||||
chr10:14008135-14008380 | Rare:56 | ||||
chr10:14838029-14838386 | Common:2; Rare:100 | ||||
chr10:14878597-14878890 | Common:2; Rare:94 | ||||
chr10:14954023-14954195 | Rare:61 | ||||
chr10:15097304-15097378 | Common:1; Rare:33 | ||||
chr10:17228463-17228675 | Common:1; Rare:57 |