chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147514341147514342TC21GENIChomozygous112874500
4147514541147514542AG15GENIChomozygous112874501
4147515921147515922GT16GENIChomozygous112874503
4147516195147516196AG21GENIChomozygous112874504
4147516424147516425GA31GENIChomozygous112874505
4147517192147517193GA7GENIChomozygous112874506
4147517943147517944CT7GENIChomozygous112874508
4147518342147518343GT22GENIChomozygous112874509
4147518419147518420TC33GENIChomozygous112874510
4147519124147519125AG16GENIChomozygous112874511
4147520349147520350CT24GENIChomozygous112874514
4147521136147521137TC30GENIChomozygous112874515
4147521373147521374TC27GENIChomozygous112874517
4147521476147521477GA9GENIChomozygous112874518
4147521625147521626CA14GENIChomozygous112874519
4147522397147522398TC21GENIChomozygous112874520
4147522690147522691TC19GENIChomozygous112874522
4147524728147524729AG27GENIChomozygous112874523
4147524988147524989TC22GENIChomozygous112874524
4147526580147526581GA27GENIChomozygous126119182
4147517168147517169GA7GENIChomozygous126119179
4147522016147522017GT4GENIChomozygous126119180
4147526542147526543CT18GENIChomozygous126119181
4147517276147517277AT9GENIChomozygous113059314
4147517278147517279TG6GENIChomozygous119281736
4147517279147517280AT10GENIChomozygous119281738
4147521491147521492AT5GENICheterozygous126054077
4147521492147521493CT3GENICheterozygous126054078
4147526134147526135AC12GENIChomozygous126025085
4147526631147526632GA22GENIChomozygous126119183
4147528692147528693GA10GENIChomozygous112874526
4147528698147528699CA13GENIChomozygous126119184
4147529237147529238CT17GENIChomozygous112874527
4147529684147529685AG27GENIChomozygous112874528
4147529804147529805GA20GENIChomozygous112874529
4147530560147530561AG21GENIChomozygous112874530
4147530658147530659CT14GENIChomozygous112874531
4147531958147531959AC10GENIChomozygous112874534