chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157247631157247632GT18GENIChomozygous785328680
5157249288157249289AG21GENIChomozygous785328681
5157249348157249349GC27GENIChomozygous785328682
5157250391157250392GC16GENIChomozygous785328683
5157251230157251231AT25GENIChomozygous785328684
5157251778157251779AC24GENIChomozygous785328685
5157251953157251954TC22GENIChomozygous785328686
5157252817157252818TA25GENIChomozygous785328687
5157252823157252824TC23GENIChomozygous785328688
5157253307157253308CA19GENIChomozygous785328689
5157253556157253557GA21GENIChomozygous785328690
5157254353157254354AG13GENIChomozygous785328691
5157254427157254428CA16GENIChomozygous785328692
5157254571157254572CT15GENICpossibly homozygous785328693
5157254586157254587TC15GENIChomozygous785328694
5157254587157254588GA15GENIChomozygous785328695
5157254657157254658AG20GENIChomozygous785328696
5157254884157254885AG21GENIChomozygous785328697
5157255531157255532GA16GENICpossibly homozygous785328698
5157256480157256481CT36GENIChomozygous785328699
5157257110157257111GA9GENICheterozygous785328700
5157257112157257113GA9GENICheterozygous785328701
5157258939157258940CA19GENIChomozygous785328702
5157259659157259660AC22GENIChomozygous785328703
5157260361157260362CT26GENIChomozygous785328704
5157262378157262379AG18GENIChomozygous785328705
5157262635157262636TC22GENIChomozygous785328706
5157262643157262644CT20GENIChomozygous785328707
5157262840157262841AG26GENIChomozygous785328708
5157263309157263310AG13GENIChomozygous785328709
5157263539157263540GA28GENIChomozygous785328710
5157263980157263981AG27GENIChomozygous785328711
5157264515157264516TC19GENIChomozygous785328712
5157265390157265391TC22GENIChomozygous785328713
5157266906157266907AG9GENIChomozygous785328714
5157268052157268053TC31GENIChomozygous785328715
5157268323157268324CT26GENIChomozygous785328716