chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101325358813253589AG47GENIChomozygous138725787
101325377313253773C43GENICpossibly homozygous138668999
101325440213254403GA46GENIChomozygous143442398
101326008913260091AC32GENICpossibly homozygous138669000
101326071913260720CT52GENIChomozygous143442401
101326141313261414AG69GENIChomozygous138725793
101326321413263215AG57GENIChomozygous138725796
101326365413263655TC67GENIChomozygous142217064
101326403813264039TC51GENIChomozygous138725798
101326407213264073CA55GENICpossibly homozygous143442402
101327327913273280CT55GENIChomozygous143442403
101327618513276186CA54GENIChomozygous143442404
101327757913277580AC49GENIChomozygous142217077
101327763413277635TC54GENIChomozygous142217078
101327768813277689AC58GENIChomozygous142217079
101327775813277759TC66GENIChomozygous142217080
101327781013277811AC57GENIChomozygous142217081