Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:11948756-11948826 | Rare:12 | ||||
chr10:11952197-11952451 | Common:1; Rare:63 | ||||
chr10:12163366-12163649 | Common:1; Rare:52 | ||||
chr10:12167750-12168007 | Common:3; Rare:69 | ||||
chr10:12171226-12171451 | Common:1; Rare:46 | ||||
chr10:12184887-12185236 | Rare:58 | ||||
chr10:12186333-12186609 | Common:1; Rare:56 | ||||
chr10:12209777-12210021 | Common:1; Rare:59 | ||||
chr10:12277724-12277866 | Rare:20 | ||||
chr10:12329196-12329214 | Rare:6 | ||||
chr10:13109690-13109714 | Rare:9 | ||||
chr10:13123992-13124336 | Common:1; Rare:76; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr10:13125404-13125931 | Common:2; Rare:120 | ||||
chr10:13451346-13451372 | Rare:5 | ||||
chr10:13527993-13528293 | Rare:83 |