chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14761766447617665T-17GENIChomozygous60697860
14761839847618399CT26GENIChomozygous61410407
14761977847619779AC28GENIChomozygous61410408
14762049947620500CT23GENIChomozygous61410409
14762095347620954GA29GENIChomozygous61410410
14762124947621250AG23GENIChomozygous60697861
14762318147623182GA23GENIChomozygous61410411
14762555247625553AG17GENICpossibly homozygous61410412
14762557747625578AATTTT5GENIChomozygous60697862
14762611847626119AG31GENIChomozygous61410413
14762816547628166TC22GENIChomozygous60697866
14762987847629879CCAAA4GENIChomozygous60697867
14762989647629897GA17GENICheterozygous60697868
14763216747632168TC28GENIChomozygous60697870
14763322847633230AG--3GENIChomozygous60697871
14763359947633600TC27GENIChomozygous60697873
14763443647634437GA20GENIChomozygous61410414
14763520247635206TGTG----28GENICheterozygous61410415
14763521147635212GA36GENICheterozygous61410416
14763521647635217TC38GENICheterozygous61410417
14763619747636198GA42GENIChomozygous61410418
14763840547638406AG23GENIChomozygous60697876
14764060447640606AC--17GENICpossibly homozygous60697878
14764094447640945T-25GENICheterozygous60697879
14764112447641125TTACACAC15GENIChomozygous61410419
14764117647641180GTGT----19GENICheterozygous60697881
14764117847641180GT--19GENICpossibly homozygous61410420
14764369347643694CT24GENIChomozygous61410421
14763524447635246CA--1GENIChomozygous61666152