chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1589007548900755CT28GENIChomozygous112449107
1589415248941525GA24GENICheterozygous112449111
1589415278941528GA27GENICheterozygous112449113
1589415338941534GA24GENICheterozygous113069963
1589415358941536CA26GENICheterozygous113069964
1590250209025021AT3GENIChomozygous112449115
1590250219025022AC3GENIChomozygous112449117
1590261849026185TA12GENIChomozygous112449119
1590261919026192TG12GENIChomozygous112449120
1590291149029115AC10GENIChomozygous112449122
1590556519055652AT10GENIChomozygous112449124
1591458719145872CT19GENIChomozygous112449128
1591458989145899CT20GENIChomozygous112449130
1591461009146101AG22GENIChomozygous112449131
1591461489146149TC26GENIChomozygous112449133
1591461699146170GA23GENIChomozygous112449135
1591462019146202CT24GENIChomozygous112449137
1591462429146243AG22GENIChomozygous112449139
1591468309146831TA12GENIChomozygous112449141
1591468839146884GA10GENIChomozygous112449143
1591561359156136AC30GENIChomozygous112449151