chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1165515768165515769CT4GENIChomozygous954026442
1165516032165516033AG20GENIChomozygous954026443
1165516316165516317GA35GENIChomozygous954026444
1165516385165516386TC36GENIChomozygous954026445
1165516956165516957GA39GENIChomozygous954026446
1165517271165517272GC25GENIChomozygous954026447
1165519823165519824TC26GENIChomozygous954026448
1165520851165520852GA42GENIChomozygous954026449
1165521025165521026CT32GENIChomozygous954026450
1165521467165521468GT36GENIChomozygous954026451
1165521468165521469AG39GENIChomozygous954026452
1165521576165521577GA51GENIChomozygous954026453
1165522002165522003CT33GENIChomozygous954026454
1165522405165522406CT20GENIChomozygous954026455
1165522406165522407CG19GENIChomozygous954026456
1165523734165523735GT17GENIChomozygous954026457
1165523762165523763CT20GENIChomozygous954026458
1165524310165524311TC19GENIChomozygous954026459
1165524973165524974TA9GENIChomozygous954026460
1165525629165525630TC39GENIChomozygous954026461
1165525770165525771TC35GENIChomozygous954026462
1165526964165526965TC31GENIChomozygous954026463
1165527324165527325CA27GENIChomozygous954026464
1165527481165527482AG26GENIChomozygous954026465
1165527942165527943CT18GENIChomozygous954026466
1165528020165528021CA18GENIChomozygous954026467
1165528136165528137AC14GENIChomozygous954026468
1165528448165528449CG29GENIChomozygous954026469
1165528468165528469TG31GENIChomozygous954026470
1165528554165528555TC34GENIChomozygous954026471
1165528709165528710CG35GENIChomozygous954026472
1165528792165528793AT21GENIChomozygous954026473
1165528959165528960AG29GENICpossibly homozygous954026474
1165529106165529107GA24GENICpossibly homozygous954026475
1165529198165529199CT23GENIChomozygous954026476