chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23068589230685893AG63GENIChomozygous109675582
23068610130686102GT52GENIChomozygous109675584
23068656630686567GC40GENIChomozygous109675586
23068694130686942GT24GENIChomozygous109675588
23068700730687008AG24GENIChomozygous109675590
23068747630687477CG35GENIChomozygous109675592
23068785130687852GT53GENIChomozygous109675594
23068815530688156GC36GENICpossibly homozygous109675596
23068922330689224AG42GENIChomozygous109675598
23068964430689645GC34GENIChomozygous109675600
23069019930690200CT41GENIChomozygous109675602
23069020530690206CT39GENIChomozygous109675604
23069074430690745CT23GENIChomozygous109675606
23069081030690811TG33GENIChomozygous109675608
23069114730691148AT30GENIChomozygous109675610
23069121030691211TA38GENIChomozygous109675612
23069218030692181GA30GENIChomozygous109675614
23069249630692497AT21GENICpossibly homozygous109675616
23069250030692501AT20GENICpossibly homozygous109675618
23069250430692505AT21GENICpossibly homozygous109675620
23069325030693251AC8GENICheterozygous109675622
23069325830693259CT9GENICheterozygous109675624
23069326130693262CT10GENICheterozygous109675626
23069326530693266TC10GENICheterozygous109675628
23069355430693555TA24GENICheterozygous109675630
23069492330694924CT32GENIChomozygous109675631
23069558730695588AG42GENIChomozygous109675633
23069625530696256GA36GENIChomozygous109675635
23069664430696645GA39GENIChomozygous109675637
23069748930697490TC33GENIChomozygous109675639
23071181930711820CG50GENIChomozygous109675641
23071617230716173GA23GENICheterozygous109675643
23072616530726166CT4GENIChomozygous109675645
23072619330726194TG8GENIChomozygous109675647
23072619630726197TC8GENIChomozygous109675649
23072621630726217TC18GENIChomozygous109675651