chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106836450106836450G39GENIChomozygous128857576
10106837729106837730GT50GENIChomozygous118012652
10106837742106837743GT47GENIChomozygous118012653
10106837755106837756GT44GENIChomozygous118012654
10106837853106837854GT9GENIChomozygous116961714
10106837881106837882GT3GENIChomozygous116961716
10106837882106837883TC3GENIChomozygous116961718
10106837887106837888G1GENIChomozygous133005862
10106841699106841699TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA10GENICpossibly homozygous128857577
10106841742106841743AG11GENICpossibly homozygous118012657