chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101509105115091052TC11GENIChomozygous116497622
101509106815091069TC14GENIChomozygous116497624
101509110115091102TC17GENIChomozygous116497626
101509136415091365CT9GENIChomozygous116497628
101509136615091367GT10GENIChomozygous116497630
101509164415091645AG29GENIChomozygous116497632
101509180315091804GA3GENICheterozygous116859924
101509188715091888AG11GENICheterozygous116737562
101509191815091919AG9GENICheterozygous116859927
101509193415091935CT9GENICheterozygous116859929
101509196115091962AG12GENICheterozygous116737563
101509198315091984CT12GENICheterozygous116497636
101509199715091998AG9GENICheterozygous116497638
101509213415092135AC15GENIChomozygous116497640
101509248515092486GA20GENIChomozygous116497642
101509250315092504GA10GENIChomozygous116497644
101509251715092518AC12GENIChomozygous116497646
101509252715092528CT13GENIChomozygous116497648
101509254515092546AG12GENIChomozygous116497650
101509271915092720AG13GENIChomozygous116497658
101509276315092764CA8GENIChomozygous116497660
101509280215092803GA18GENIChomozygous116497662
101509303515093036GA24GENIChomozygous116497664
101509307815093079CG22GENIChomozygous116497666
101509311215093113CT15GENIChomozygous116497668
101509323815093239CT25GENIChomozygous116497670
101509339715093398AG22GENIChomozygous116497672
101509358515093586CT9GENICheterozygous116497674
101509374815093749AG21GENIChomozygous116497676
101509393315093934GA7GENIChomozygous116497678
101509419415094195GA6GENIChomozygous116497680
101509419715094198AG7GENIChomozygous116497682
101509419815094199GC7GENIChomozygous116497684
101509431315094314GA21GENIChomozygous116497686
101509443615094437GT22GENIChomozygous116497690
101509479715094798GA8GENICheterozygous116497692
101509480015094801TC6GENICheterozygous116497694
101509503715095038AG22GENIChomozygous116497698
101509630115096302GA19GENICheterozygous116497702
101509676015096761TG22GENIChomozygous116497704
101509844615098447GA4GENICheterozygous116497706