chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
202828397228283973AG40GENIChomozygous130073460
202828671228286713AT26GENIChomozygous130073461
202828790228287903CT24GENIChomozygous130073462
202828858328288584C14GENIChomozygous129989510
202828977128289772G32GENIChomozygous129989512
202829052628290527CT34GENIChomozygous130073463
202829112728291128T16GENICpossibly homozygous129989515
202829214528292146GA27GENIChomozygous130073464
202829307428293075TG33GENICpossibly homozygous130073465
202829346328293464CT35GENIChomozygous130073466
202829346428293465CT35GENIChomozygous130073467
202829371028293711GA26GENICpossibly homozygous130073468
202829391628293917AG30GENIChomozygous130073469
202829429828294299CT20GENIChomozygous130073470
202829441928294420CT21GENIChomozygous130073471
202829442228294423CT22GENIChomozygous130073472
202829655128296552AT34GENIChomozygous130073473
202829660428296605TC31GENIChomozygous130073474
202829666428296665AT30GENIChomozygous130073475
202829729128297291A31GENIChomozygous129989518
202829736228297363GC34GENIChomozygous130073476
202829758128297582CT19GENIChomozygous130073477
202829891928298920GA25GENIChomozygous130073478
202830024628300248TG22GENIChomozygous129989520
202830035328300354CT19GENIChomozygous130073479
202830037228300383GTGTGTGGTGT14GENIChomozygous129989523
202830075128300752TC22GENIChomozygous130073480
202830132928301330TC28GENIChomozygous130073481
202830182028301820GTC26GENIChomozygous129989526
202830260428302605C20GENICpossibly homozygous129989528
202830321628303217G13GENIChomozygous129989531
202830328728303288TA22GENIChomozygous130073482
202830370228303703AG28GENIChomozygous130073483
202830438028304381TC29GENIChomozygous130073484
202830492128304922TC37GENIChomozygous130073485
202830536928305370CT24GENIChomozygous130073486
202830551728305518TC23GENIChomozygous130073487
202830551828305519GC23GENIChomozygous130073488
202830650928306510GT26GENIChomozygous130073489