chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31760458517604586GT33GENIChomozygous112412999
31760464117604642AG42GENIChomozygous112413001
31760465817604659TA45GENIChomozygous112413003
31760469117604692GA49GENIChomozygous112413005
31760473917604740TC48GENIChomozygous112413007
31760501217605013GA44GENIChomozygous112413010
31760501717605018AG42GENIChomozygous112413013
31760507017605071AG51GENIChomozygous112413015
31760510217605103GA47GENIChomozygous112413017
31760520617605207CT53GENICpossibly homozygous112413019
31760522817605229CA51GENICpossibly homozygous112413021
31760523717605238GC48GENICpossibly homozygous112413023
31760531817605319CT40GENIChomozygous112413025
31760536617605367CT52GENIChomozygous112413027
31760556117605562CT55GENIChomozygous112413029
31760556617605567GA53GENIChomozygous112413031
31760575317605754AC38GENIChomozygous112413033
31760581117605812AG26GENIChomozygous112413035
31760581617605817TA22GENIChomozygous112413037
31760586417605865CG27GENIChomozygous112413039
31760593717605938TC36GENIChomozygous112413041
31760595017605951TC37GENIChomozygous112413043
31760603117606032AG38GENIChomozygous112413045
31760605017606051CT40GENIChomozygous112413047
31760659717606598AG49GENIChomozygous112413049
31760667117606672TA51GENIChomozygous112413051
31760712717607128GC70GENIChomozygous112413053
31760735817607359AG47GENIChomozygous112413055
31760757417607575TG43GENIChomozygous112413057