chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143208061143208062AT24GENIChomozygous116099382
7143208561143208562AG10GENIChomozygous115942953
7143209506143209507CG18GENIChomozygous116099384
7143209899143209900AT16GENIChomozygous115942954
7143209973143209974GC20GENIChomozygous115942955
7143210038143210039TC20GENIChomozygous115942956
7143210468143210469AG13GENICheterozygous116099386
7143211158143211159CT18GENIChomozygous116099388
7143211647143211648GT23GENIChomozygous115942958
7143212349143212350TC13GENIChomozygous115942960
7143212613143212614TC29GENIChomozygous115942961
7143212825143212826AG15GENIChomozygous115942962
7143212917143212918TG12GENIChomozygous116099390
7143214047143214048TG22GENIChomozygous116099392
7143214166143214167TC22GENIChomozygous116099394
7143214266143214267TC14GENIChomozygous116099396
7143214300143214301CG13GENIChomozygous116099398
7143214353143214354TC12GENIChomozygous116099400
7143215058143215059GA21GENIChomozygous116099402
7143215228143215229AG10GENIChomozygous116099404
7143215413143215414TC21GENIChomozygous116099406
7143215598143215599CA25GENIChomozygous116099408
7143215809143215810AG20GENIChomozygous116099410
7143217393143217394CT32GENIChomozygous115942967