chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17145222671452227CT18GENIChomozygous108863571
17145355171453552CG16GENIChomozygous108863573
17146056671460567GA22GENIChomozygous109560721
17146094571460946AC32GENIChomozygous108863596
17146102571461026AC29GENIChomozygous108863597
17146286471462865AG28GENIChomozygous109560722
17146824071468241GA33GENIChomozygous108132053
17146868971468690AC31GENIChomozygous120893699
17146958071469581TG32GENIChomozygous108863619
17147070571470706CT24GENIChomozygous108863629
17147099671470997GA27GENIChomozygous109560724
17147139971471400CT30GENIChomozygous108132118
17147182871471829CT20GENIChomozygous109560725
17147270071472701TC37GENIChomozygous108863634
17147290071472901AG33GENIChomozygous108863635
17147315271473153GA25GENIChomozygous109560726
17147353671473537CT12GENIChomozygous108863636
17147373371473734AC20GENIChomozygous108863637
17147424871474249CA31GENIChomozygous108863638
17147517871475179AG21GENIChomozygous108863643
17147518871475189TC17GENIChomozygous108863644
17147520771475208TC18GENIChomozygous108863645
17147521171475212AG18GENIChomozygous108863646
17147524771475248AG25GENIChomozygous109560729
17147575571475756GA32GENIChomozygous109291401
17147585671475857AG22GENIChomozygous108863648
17147589471475895GA13GENIChomozygous108863649
17147656471476565CT17GENIChomozygous108863650
17147680671476807GA27GENIChomozygous108863651
17147701971477020CG35GENIChomozygous108863652
17147740071477401CT32GENIChomozygous109496020
17147816871478169TC18GENIChomozygous108863653
17147832371478324CT27GENIChomozygous108863654
17147832471478325CG27GENIChomozygous108863655
17147879671478797CT18GENIChomozygous108863656
17147919871479199CT35GENIChomozygous108863659
17147983071479831AC38GENIChomozygous108863660
17148037671480377CT19GENIChomozygous109496021
17148569971485700CT20GENIChomozygous108863683