chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31682535316825354TC34GENIChomozygous58086695
31682564516825646TA35GENIChomozygous58086697
31682633716826338CT35GENIChomozygous58086699
31682674016826741CT29GENIChomozygous58086701
31682705716827058GA34GENICpossibly homozygous58086703
31682729516827297CT--30GENIChomozygous58086705
31682765916827660TC33GENIChomozygous58086707
31682769716827709TCAACCAGACTC------------24GENIChomozygous58086709
31682786516827866TC17GENIChomozygous58086712
31682795416827955AG21GENIChomozygous58086714
31682801316828014AG34GENIChomozygous58086716
31682812816828129AG29GENIChomozygous58086718
31682818316828184CG22GENIChomozygous58086720
31682856216828563CT27GENICpossibly homozygous58086722
31682863716828638CT31GENICpossibly homozygous58086724
31682933116829332AG28GENICpossibly homozygous57174005
31682809116828092AG22GENIChomozygous57173999
31682967316829674T-23GENICpossibly homozygous58086728
31683003416830035AG28GENIChomozygous58086730
31683049716830498CT23GENIChomozygous58086732
31683062816830629CG26GENIChomozygous58086734
31683071216830713CCCCCCG16GENIChomozygous58086736
31683084716830848AG26GENIChomozygous58086738
31683126016831261GA29GENIChomozygous58086740
31683147816831479A-21GENIChomozygous58086742