Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12348957-12349250 | Common:3; Rare:68 | ||||
chr10:12349363-12349628 | Common:2; Rare:64 | ||||
chr10:12349688-12349990 | Common:1; Rare:89 | ||||
chr10:13001701-13001870 | Rare:50 | ||||
chr10:13099797-13099917 | Rare:28 | ||||
chr10:13099920-13100273 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13100583-13100698 | Common:1; Rare:22 | ||||
chr10:13161246-13161647 | Common:1; Rare:111 | ||||
chr10:13161816-13161950 | Common:2; Rare:24 | ||||
chr10:13299268-13299387 | Common:2; Rare:28 | ||||
chr10:13299440-13299844 | Common:7; Rare:87 | ||||
chr10:13299928-13300235 | Rare:104; Clinvar:2 | ||||
chr10:13302058-13302236 | Common:2; Rare:28 | ||||
chr10:13302263-13302598 | Rare:68 | ||||
chr10:13347255-13347497 | Common:2; Rare:83 |