chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18017104280171042A14GENIChomozygous131258302
18017118680171187GA10GENIChomozygous109298332
18017194180171942AT16GENIChomozygous109298334
18017203280172033TC14GENIChomozygous109298336
18017368580173686GA18GENIChomozygous133660158
18017400380174004CT23GENIChomozygous109298338
18017421980174220AC10GENIChomozygous109298340
18017443180174432AC19GENIChomozygous109298344
18017582080175821TC18GENIChomozygous109298347
18017590880175909TA19GENIChomozygous109298349
18017677480176775TC18GENIChomozygous109298351
18017697880176978GGGA6GENIChomozygous131575746
18017743980177440AG19GENIChomozygous109298353
18017799780178001CTGT19GENIChomozygous131258303
18018073580180736AT18GENIChomozygous109298355
18018080180180802CT16GENIChomozygous109298357
18018118180181182TC18GENIChomozygous109298359
18018201480182015GA13GENIChomozygous109298361
18018242580182426AG15GENICpossibly homozygous109298363
18018313680183137AG17GENIChomozygous109298367
18018501780185017CCG13GENIChomozygous127397505
18018545580185456CA11GENIChomozygous120868283
18018586380185864CG15GENIChomozygous109298369