chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168130956481309565AG34GENIChomozygous47566100
168130960881309609TC49GENIChomozygous47566102
168131038781310388GA14GENIChomozygous47566104
168131185581311856AAGGAGGCTGGCCCATGGGAACCTTGGGCTTTGGACGTTTGGGGGT30GENIChomozygous48022983
168131264481312645TA12GENIChomozygous47566106
168131275181312752AAAATAATAATAATAATAAT5GENIChomozygous48022984
168131350381313504CT34GENIChomozygous47566115
168131578581315786GA24GENICpossibly homozygous47566117
168131776981317773TGTG----6GENIChomozygous48022985
168131787281317873GGGTGTGT16GENICpossibly homozygous47997966
168132026581320266TC14GENICpossibly homozygous47566123