chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147514341147514342TC12GENIChomozygous112874500
4147514541147514542AG21GENIChomozygous112874501
4147515892147515893AG23GENICpossibly homozygous112874502
4147515921147515922GT25GENICpossibly homozygous112874503
4147516195147516196AG25GENIChomozygous112874504
4147516424147516425GA53GENICpossibly homozygous112874505
4147517192147517193GA18GENIChomozygous112874506
4147517276147517277AT25GENIChomozygous113059314
4147517278147517279TG23GENIChomozygous119281736
4147517279147517280AT23GENIChomozygous119281738
4147517933147517934CG33GENIChomozygous112874507
4147517943147517944CT34GENIChomozygous112874508
4147518342147518343GT30GENICpossibly homozygous112874509
4147518419147518420TC26GENIChomozygous112874510
4147519124147519125AG20GENIChomozygous112874511
4147519515147519516GA34GENIChomozygous112874512
4147520349147520350CT34GENICpossibly homozygous112874514
4147521136147521137TC24GENICpossibly homozygous112874515
4147521218147521219CT27GENIChomozygous112874516
4147521373147521374TC33GENIChomozygous112874517
4147521476147521477GA32GENIChomozygous112874518
4147521625147521626CA20GENIChomozygous112874519
4147522397147522398TC35GENIChomozygous112874520
4147522528147522529GA32GENIChomozygous112874521
4147522690147522691TC21GENIChomozygous112874522
4147524728147524729AG30GENIChomozygous112874523
4147524988147524989TC50GENICpossibly homozygous112874524
4147526457147526458TG31GENIChomozygous112874525
4147528692147528693GA35GENIChomozygous112874526
4147529237147529238CT30GENIChomozygous112874527
4147529684147529685AG30GENIChomozygous112874528
4147529804147529805GA34GENIChomozygous112874529
4147530560147530561AG35GENIChomozygous112874530
4147530658147530659CT26GENIChomozygous112874531
4147531417147531418CG31GENIChomozygous112874532
4147531579147531580GA36GENIChomozygous112874533
4147531958147531959AC20GENIChomozygous112874534