chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214609684214609685CT42GENIChomozygous108990454
1214609814214609815TG42GENICpossibly homozygous108990455
1214610026214610026TT45GENIChomozygous131781873
1214610550214610551CT42GENIChomozygous108990456
1214610565214610566GA41GENIChomozygous108990457
1214610611214610612CT41GENIChomozygous108990458
1214610830214610831GA25GENIChomozygous108990459
1214611043214611044AG35GENIChomozygous108990460
1214611218214611219GC28GENIChomozygous108532480
1214611293214611294GT20GENIChomozygous108990461
1214611699214611700TA50GENICheterozygous108990462
1214611700214611701GA53GENICheterozygous108532483
1214611898214611899GA15GENICpossibly homozygous108990463
1214612486214612487TA1GENIChomozygous130852494
1214613227214613228GA115GENICheterozygous108990464
1214613242214613243CG101GENICheterozygous108990465
1214613253214613254CT90GENIChomozygous108532485
1214613425214613426GA17GENICheterozygous108990466
1214613526214613527TC25GENICheterozygous131796116
1214611999214612000TC22GENICheterozygous131796113
1214612774214612775TA23GENICheterozygous131796115
1214613611214613612CG19GENICheterozygous131796117
1214614780214614781CT139GENIChomozygous108532486
1214615053214615054TC30GENICheterozygous133807557
1214615104214615105CG42GENICheterozygous131796119
1214616316214616317TG40GENIChomozygous108532487
1214619489214619490GA35GENIChomozygous108990467
1214621090214621091AG41GENIChomozygous108532491
1214621601214621602TC39GENIChomozygous108990468
1214625456214625457TC40GENIChomozygous108532492
1214628089214628090TG32GENIChomozygous108532498
1214628090214628091TC32GENIChomozygous108532499
1214628823214628824TC37GENIChomozygous108532500
1214629427214629428CG39GENIChomozygous108532502