chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159932992499329925TG16GENIChomozygous112759883
159933038099330381GT21GENIChomozygous112759885
159933042999330430GC19GENIChomozygous112759887
159933044399330444TA14GENIChomozygous112614757
159933080299330803CA9GENIChomozygous112614759
159933388699333887TA10GENIChomozygous112759897
159933851199338512TA21GENIChomozygous112614778
159933909599339096AT13GENIChomozygous112614780
159934010699340107AG17GENIChomozygous112614782
159934085699340857CT8GENICheterozygous112614784
159934140199341402TC8GENIChomozygous112614786
159934213399342134AT12GENIChomozygous112614788
159934259099342591TA14GENIChomozygous112614790
159934485099344851GT5GENIChomozygous112614792
159934546899345469TA16GENIChomozygous112614794
159934586899345869GT15GENIChomozygous112614796