chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143208061143208062AT32GENIChomozygous116099382
7143208561143208562AG31GENIChomozygous115942953
7143209506143209507CG36GENIChomozygous116099384
7143209899143209900AT23GENIChomozygous115942954
7143209973143209974GC20GENIChomozygous115942955
7143210038143210039TC31GENIChomozygous115942956
7143210468143210469AG40GENIChomozygous116099386
7143211397143211398AC27GENIChomozygous115942957
7143211647143211648GT30GENIChomozygous115942958
7143212349143212350TC31GENIChomozygous115942960
7143212825143212826AG39GENIChomozygous115942962
7143212917143212918TG34GENIChomozygous116099390
7143214047143214048TG38GENIChomozygous116099392
7143214166143214167TC38GENIChomozygous116099394
7143214266143214267TC36GENIChomozygous116099396
7143214300143214301CG32GENIChomozygous116099398
7143214353143214354TC29GENIChomozygous116099400
7143215058143215059GA32GENIChomozygous116099402
7143215228143215229AG32GENIChomozygous116099404
7143215413143215414TC48GENIChomozygous116099406
7143215598143215599CA36GENIChomozygous116099408
7143215809143215810AG37GENIChomozygous116099410
7143217393143217394CT36GENIChomozygous115942967