chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109202185992021860GA20GENIChomozygous116952582
109202549892025499CT22GENIChomozygous116952584
109202630292026303CT27GENIChomozygous116952586
109202677792026778CT22GENIChomozygous116952588
109202805992028060TA20GENIChomozygous116679089
109202810692028107AG12GENIChomozygous116952590
109202976992029770AG14GENIChomozygous116679093
109202978292029783GA16GENIChomozygous116906399
109202989792029898AG25GENIChomozygous116679097
109202989992029900GT25GENIChomozygous116679099
109203073392030734TC17GENIChomozygous116906403
109203102092031021CT19GENICpossibly homozygous117020966
109203103692031037CA18GENICpossibly homozygous118008159
109203123192031232GA20GENIChomozygous117133888
109203135392031354AT23GENIChomozygous118008160
109203146792031468GC28GENIChomozygous116679107
109203165392031654TC15GENIChomozygous116822910
109203272292032723CA14GENIChomozygous116952592
109203279492032795CT15GENIChomozygous116679109
109203300692033007TC32GENIChomozygous116679111
109203312092033121TA28GENIChomozygous116952594
109203312192033122CA28GENIChomozygous116952596
109203414092034141CG19GENIChomozygous116679113
109203443892034439CT22GENIChomozygous116952598
109203533192035332CG17GENIChomozygous116822912
109203732692037327CT19GENIChomozygous116952600
109203751992037520TC19GENIChomozygous116679115
109203954092039541GT27GENIChomozygous116679121
109204013492040135CT22GENIChomozygous116952602
109203100092031001TA21GENIChomozygous117328733