Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:74070667-74071083 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):8 | ||||
chr10:74109526-74109598 | Common:1; Rare:11 | ||||
chr10:74111661-74112050 | Common:2; Rare:107; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr10:74114586-74114896 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
chr10:75230782-75230963 | Common:1; Rare:45 | ||||
chr10:75403542-75403567 | Rare:4 | ||||
chr10:77925358-77925702 | Rare:57 | ||||
chr10:79826315-79826894 | Common:5; Rare:172 | ||||
chr10:80207323-80207452 | Rare:26 | ||||
chr10:86755706-86755896 | Rare:44 | ||||
chr10:86955615-86955791 | Rare:27 | ||||
chr10:86971194-86971468 | Common:2; Rare:91 | ||||
chr10:87342283-87342425 | Common:3; Rare:45 | ||||
chr10:87342625-87342942 | Common:1; Rare:76 | ||||
chr10:88939492-88939847 | Rare:67; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 |