chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67605695276056953GA20GENIChomozygous114862241
67605709076057091AG21GENIChomozygous114862242
67605894876058949CT20GENIChomozygous115258482
67606047076060471TC22GENIChomozygous114862243
67606452776064528CT27GENIChomozygous115258484
67606488576064886TG29GENIChomozygous114862245
67606663376066634CT21GENIChomozygous115258486
67606749776067498AT26GENIChomozygous114862248
67606492976064930GA26GENIChomozygous114862246
67606686376066864CT21GENIChomozygous114862247
67606767876067679CT19GENIChomozygous114862249
67606829176068292TA23GENIChomozygous114862250
67606999176069992CT29GENIChomozygous114862254
67607018376070184AG32GENIChomozygous114862255
67607046876070469AG11GENIChomozygous114862256
67607092576070926CG11GENIChomozygous114862257
67607183276071833GA28GENIChomozygous114862259
67607228276072283AG26GENIChomozygous114862260
67607285376072854GA25GENICpossibly homozygous114862261
67607302176073022GA19GENICpossibly homozygous114862262
67607339476073395GT19GENIChomozygous114862263
67607342476073425CT16GENIChomozygous114862264
67607347576073476TC26GENIChomozygous114862265
67607348376073484AG26GENIChomozygous114862266
67607697076076971TC18GENIChomozygous114862275
67607701076077011GA25GENIChomozygous114862276
67607707976077080GA21GENIChomozygous114862277
67607799176077992GA35GENIChomozygous114862278
67607881176078812AG28GENIChomozygous114862279
67607901676079017CT36GENIChomozygous115258490
67607904976079050GA30GENIChomozygous115258492