chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109202549892025499CT25GENIChomozygous116952584
109202630292026303CT17GENIChomozygous116952586
109202677792026778CT16GENIChomozygous116952588
109202805992028060TA8GENIChomozygous116679089
109202810692028107AG14GENIChomozygous116952590
109202958992029590TA5GENICheterozygous118129959
109202976992029770AG8GENIChomozygous116679093
109202978292029783GA10GENIChomozygous116906399
109202989792029898AG20GENIChomozygous116679097
109202989992029900GT20GENIChomozygous116679099
109203073392030734TC26GENIChomozygous116906403
109203100092031001TA28GENIChomozygous117328733
109203102092031021CT30GENIChomozygous117020966
109203103692031037CA31GENICpossibly homozygous118008159
109203135392031354AT23GENIChomozygous118008160
109203146792031468GC27GENIChomozygous116679107
109203165392031654TC20GENICpossibly homozygous116822910
109203272292032723CA27GENIChomozygous116952592
109203279492032795CT20GENIChomozygous116679109
109203300692033007TC23GENIChomozygous116679111
109203414092034141CG24GENIChomozygous116679113
109203443892034439CT29GENIChomozygous116952598
109203533192035332CG20GENIChomozygous116822912
109203732692037327CT32GENIChomozygous116952600
109203751992037520TC22GENIChomozygous116679115
109203954092039541GT21GENIChomozygous116679121
109204013492040135CT29GENIChomozygous116952602
109203123192031232GA17GENIChomozygous117133888