chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4123109078123109079GA20GENICheterozygous113155690
4123109365123109366GA11GENIChomozygous113049330
4123110045123110046CG25GENIChomozygous113155691
4123110223123110224AG38GENIChomozygous113155692
4123111145123111146GA21GENIChomozygous113155693
4123111288123111289CT26GENIChomozygous113155694
4123111456123111457GT31GENIChomozygous113155695
4123111698123111699TC21GENIChomozygous113155696
4123111757123111758TC26GENIChomozygous113155697
4123112090123112091TC29GENIChomozygous113155698
4123112345123112346GA27GENIChomozygous113155699
4123112385123112386TC24GENIChomozygous113155700
4123112516123112517GA13GENIChomozygous113155701
4123112730123112731AT23GENIChomozygous113155702
4123113775123113776AC22GENIChomozygous113155703
4123113969123113970AC25GENIChomozygous113155704
4123114068123114069CT28GENIChomozygous113155705
4123114550123114551CT29GENIChomozygous113155706
4123114722123114723AC29GENIChomozygous113155707
4123114927123114928TG29GENIChomozygous113155708
4123115196123115197TC21GENIChomozygous113155709
4123115318123115319TC24GENIChomozygous113155710
4123115329123115330GA24GENIChomozygous113155711
4123115510123115511GA21GENIChomozygous113155712
4123115962123115963AG43GENIChomozygous113155713
4123116298123116299CT23GENIChomozygous113155714
4123116734123116735AG30GENIChomozygous113155715
4123117094123117095GA28GENIChomozygous113155716
4123117701123117702TC27GENIChomozygous113155717
4123117968123117969CT9GENIChomozygous113155718
4123118034123118035CT8GENIChomozygous113155719
4123118048123118049AG8GENIChomozygous113155720