chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84867849148678492CT33GENICheterozygous117002545
84867870948678710CT32GENIChomozygous117002547
84867959348679594CT20GENICpossibly homozygous116957374
84867988648679887GT57GENIChomozygous117002549
84867997848679979TC51GENIChomozygous117002551
84868060048680601TA42GENIChomozygous117002553
84868129848681299TC46GENIChomozygous117002555
84868170648681707TA52GENIChomozygous117002557
84868182248681823AG59GENIChomozygous117002559
84868262348682624GA40GENICpossibly homozygous117040042
84868273048682731AG39GENIChomozygous117002561
84868344748683448TC32GENIChomozygous117002563
84868372448683725GA49GENIChomozygous117002565
84868419948684200GA34GENIChomozygous117002567
84868488148684882AG39GENIChomozygous117002569
84868511148685112CT48GENIChomozygous117002571
84868522348685224CT38GENIChomozygous117002573
84868601948686020TC43GENIChomozygous117002575
84868606748686068TC39GENICpossibly homozygous117002577
84868714248687143CT38GENIChomozygous117002579
84868739548687396TC30GENIChomozygous117002581
84868784048687841AG49GENICpossibly homozygous117002583
84868804548688046CT50GENICpossibly homozygous117002585
84868809548688096GC45GENICpossibly homozygous117002587
84868822648688227GA60GENIChomozygous117002589
84868888948688890CT46GENIChomozygous117002591
84868916148689162GA43GENICpossibly homozygous117002593
84868918248689183CT38GENICpossibly homozygous117002595
84869005348690054TC32GENIChomozygous117002597
84869098048690981CT34GENIChomozygous117002599
84869127348691274TC42GENIChomozygous117002601
84869135848691359GC57GENIChomozygous117002603
84869160748691608AG53GENICpossibly homozygous117002605