chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105946449959464500TG4GENIChomozygous51897649
105946500559465006GA6GENIChomozygous51897651
105946522459465225GA20GENIChomozygous51897653
105946535459465355GT11GENIChomozygous51897655
105946546659465467AG7GENIChomozygous51897657
105946577859465779AT7GENIChomozygous51897659
105946601859466019TC15GENIChomozygous51897661
105946651959466520TC8GENIChomozygous51897663
105946678259466783GGT1GENIChomozygous51663412
105946696059466961TC9GENIChomozygous51897671
105946721859467219AG18GENIChomozygous51897673
105946791759467933ATATATATATATATAT----------------4GENIChomozygous51897675
105946945259469453AG10GENIChomozygous51897677
105946954359469544CT22GENIChomozygous51897679
105946975159469752TC11GENIChomozygous51897681
105947002259470023GA14GENIChomozygous51897683
105947045159470452CT12GENIChomozygous51897685
105947151459471515AG25GENIChomozygous51897687
105947225459472255GA9GENICpossibly homozygous51897689
105947229959472300CT7GENIChomozygous51897691
105947260959472624CCAAACCAAACCAAA---------------3GENIChomozygous52379096
105946794859467949TC3GENIChomozygous52379088
105946797559468001AGAGAGAGAGAGAGAGAGAGAGAGAG--------------------------5GENIChomozygous52379092
105947203159472032CCGGGGTTGGGGATTTAGCTCAGTGG7GENICheterozygous52379094
105947223259472233CG7GENIChomozygous51465616
105947569359475694GC9GENIChomozygous51897693