chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18255674282556743GC15GENIChomozygous108140545
18255675182556752TC9GENICpossibly homozygous108140546
18256092582560926GC11GENIChomozygous108140547
18256092682560927CT11GENIChomozygous108140548
18256125782561258CT14GENIChomozygous108140549
18256216082562161AT18GENIChomozygous108140550
18256220182562202CA12GENIChomozygous108140551
18256269582562696AG10GENIChomozygous108140553
18256276182562762GA22GENIChomozygous108140554
18256465382564654GT14GENIChomozygous108140555
18256857682568577CT46GENIChomozygous108140556
18256858082568581CT46GENIChomozygous108140557
18256858682568587CT49GENIChomozygous108140558
18256859082568591CT43GENIChomozygous108140559
18256859682568597CT46GENIChomozygous108140560