chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53582117935821180CT29GENIChomozygous113741754
53582126135821262GA24GENIChomozygous113741756
53582149435821495CA46GENICpossibly homozygous113741758
53582166335821664CT50GENIChomozygous113741760
53582196735821968TC65GENIChomozygous113741762
53582212735822128TC65GENIChomozygous113741764
53582284935822850GA48GENIChomozygous113741766
53582296935822970CT42GENIChomozygous113741768
53582313335823134GA40GENIChomozygous113741770
53582398235823983AG41GENIChomozygous113741772
53582665635826657TC40GENIChomozygous113741774
53582702635827027CT49GENIChomozygous113741776
53582845435828455AT20GENICpossibly homozygous113741778
53582862835828629TC48GENIChomozygous113741780
53583012435830125CG38GENICheterozygous113741782
53583048235830483TG28GENIChomozygous113741784
53583095135830952AG14GENIChomozygous113741786
53583161835831619CG32GENICpossibly homozygous113741788