chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4176996118176996119GA50GENIChomozygous112966593
4176996668176996669TC50GENIChomozygous112966595
4176996718176996719AG66GENIChomozygous112966597
4176998733176998734GA39GENIChomozygous112966599
4176999157176999158AG59GENIChomozygous112966601
4177000566177000567TC24GENIChomozygous112966603
4177001590177001591TC48GENIChomozygous112966605
4177002472177002473AG56GENIChomozygous112966607
4177002789177002790TC53GENIChomozygous112966609
4177003005177003006AT43GENICpossibly homozygous112966611
4177003308177003309AG46GENIChomozygous112966614
4177003360177003361GA46GENIChomozygous112966616
4177003821177003822CT51GENIChomozygous112966618
4177003915177003916CA60GENICpossibly homozygous112966620
4177003940177003941GA64GENIChomozygous112966622
4177004384177004385GA65GENICpossibly homozygous112966624
4177004836177004837AG57GENIChomozygous112966626
4177004914177004915CT57GENIChomozygous112966628
4177005146177005147TC59GENIChomozygous112966630
4177005712177005713AC64GENICpossibly homozygous112966632
4177005978177005979AG37GENIChomozygous112966634
4177006238177006239AG57GENIChomozygous112966636
4177006632177006633CT30GENIChomozygous112966638
4177009047177009048TC47GENIChomozygous112966640
4177009425177009426AT50GENIChomozygous112966642
4177009908177009909GA64GENICpossibly homozygous112966644
4177010292177010293TC63GENIChomozygous112966646