chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108190952108190953TA71GENIChomozygous116715448
10108190953108190954TG71GENIChomozygous116715450
10108190954108190955TA72GENIChomozygous116715452
10108190959108190960TA72GENIChomozygous116715454
10108191494108191495AT32GENIChomozygous116715456
10108191495108191496AG32GENIChomozygous116715458
10108191496108191497AG31GENIChomozygous116715460
10108191743108191743TGGCGCTCCTCGGCAGCACGTTTCTTGTGGCTGGGGGAGCGCGCCTCGCTCTCGGCTGCCTCGCCCGACTTGATCTTCACGGCCTGCATGCCGTTCTCCATGTACTTGCTCATCACGATCACGATGCGCCCATTCTTGTTCTTGTTCTTGACGATTTTCATCTTGCCCCCAATGCCATTACCGGCCACCGCCTCCTTAGGGGCTGGTG53GENICpossibly homozygous128859350
10108193974108193975CG54GENIChomozygous116715462