chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127836303127836304AG27GENIChomozygous116719440
8127836311127836312GT25GENIChomozygous116719442
8127836388127836389AT11GENIChomozygous116719444
8127836403127836404AG12GENIChomozygous116719446
8127837054127837055AT24GENIChomozygous116719450
8127837089127837090CT32GENICheterozygous116719452
8127837096127837097TA29GENIChomozygous116719454
8127837203127837204TC37GENICheterozygous116719456
8127838752127838753AC23GENIChomozygous116719458
8127839139127839140GA31GENICpossibly homozygous116719460
8127839286127839287TC24GENIChomozygous116719462
8127839486127839487AG26GENIChomozygous116719464
8127840720127840721TA24GENICpossibly homozygous116719466
8127840870127840871TC29GENIChomozygous116719468
8127840879127840880AC30GENIChomozygous116719470
8127842590127842591AG20GENIChomozygous116719472
8127843240127843241TC20GENIChomozygous116719474
8127843642127843643CT24GENIChomozygous116719476
8127843714127843715CT20GENIChomozygous116719478
8127843717127843718TC20GENIChomozygous116719480
8127844130127844131GA24GENIChomozygous116719482
8127844492127844493TA16GENIChomozygous116719484
8127844756127844757GC3GENIChomozygous116719486
8127845048127845049CT6GENIChomozygous116719488