chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109202549892025499CT27GENIChomozygous116952584
109202630292026303CT12GENIChomozygous116952586
109202677792026778CT25GENIChomozygous116952588
109202805992028060TA10GENIChomozygous116679089
109202810692028107AG12GENIChomozygous116952590
109202976992029770AG17GENIChomozygous116679093
109202978292029783GA9GENIChomozygous116906399
109202989792029898AG7GENIChomozygous116679097
109202989992029900GT7GENIChomozygous116679099
109203073392030734TC26GENIChomozygous116906403
109203146792031468GC26GENIChomozygous116679107
109203272292032723CA20GENIChomozygous116952592
109203279492032795CT26GENIChomozygous116679109
109203300692033007TC29GENIChomozygous116679111
109203414092034141CG31GENICpossibly homozygous116679113
109203443892034439CT29GENIChomozygous116952598
109203533192035332CG23GENIChomozygous116822912
109203732692037327CT17GENIChomozygous116952600
109203751992037520TC8GENIChomozygous116679115
109203954092039541GT26GENIChomozygous116679121
109204013492040135CT23GENIChomozygous116952602
109203326492033265AC7GENICheterozygous117296971