chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147514341147514342TC8GENIChomozygous112874500
4147514541147514542AG15GENIChomozygous112874501
4147515892147515893AG13GENIChomozygous112874502
4147515921147515922GT21GENIChomozygous112874503
4147516083147516084CA4GENICheterozygous126133871
4147516195147516196AG18GENIChomozygous112874504
4147516424147516425GA15GENIChomozygous112874505
4147517192147517193GA4GENIChomozygous112874506
4147517276147517277AT8GENIChomozygous113059314
4147517278147517279TG10GENIChomozygous119281736
4147517279147517280AT10GENIChomozygous119281738
4147517943147517944CT6GENIChomozygous112874508
4147518342147518343GT19GENIChomozygous112874509
4147518419147518420TC22GENIChomozygous112874510
4147519124147519125AG17GENIChomozygous112874511
4147519515147519516GA14GENIChomozygous112874512
4147520349147520350CT27GENIChomozygous112874514
4147521136147521137TC19GENIChomozygous112874515
4147521218147521219CT23GENIChomozygous112874516
4147521373147521374TC18GENIChomozygous112874517
4147521476147521477GA9GENICheterozygous112874518
4147521625147521626CA9GENICheterozygous112874519
4147522397147522398TC18GENIChomozygous112874520
4147522528147522529GA7GENIChomozygous112874521
4147522690147522691TC18GENICpossibly homozygous112874522
4147524728147524729AG24GENIChomozygous112874523
4147524988147524989TC21GENIChomozygous112874524
4147526134147526135AC11GENICheterozygous126025085
4147526457147526458TG18GENICpossibly homozygous112874525
4147528692147528693GA22GENIChomozygous112874526
4147529237147529238CT15GENIChomozygous112874527
4147529684147529685AG19GENIChomozygous112874528
4147529804147529805GA16GENIChomozygous112874529
4147530560147530561AG19GENIChomozygous112874530
4147530658147530659CT19GENIChomozygous112874531
4147531417147531418CG24GENIChomozygous112874532
4147531579147531580GA20GENIChomozygous112874533
4147531958147531959AC17GENIChomozygous112874534
4147521491147521492AT4GENICheterozygous126054077