chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
458663315866332AG13GENIChomozygous56733942
458674265867427AG21GENIChomozygous56733943
458675595867560AG25GENIChomozygous56733944
458678865867887AAAAAT1GENIChomozygous56733945
458683405868341TC14GENIChomozygous56733946
458708425870848AGACTG------27GENICpossibly homozygous56733947
458717385871739GA23GENIChomozygous56733948
458724045872405TA29GENICpossibly homozygous56733949
458730115873012T-16GENIChomozygous56733950
458730195873020TA17GENICpossibly homozygous58273875
458731045873105GA26GENIChomozygous56733951
458735685873569AC22GENIChomozygous56733952
458740525874053CT14GENICpossibly homozygous56733953
458744855874486TA24GENICpossibly homozygous56733954
458747755874776AG32GENICpossibly homozygous56733955
458752845875285CT33GENICpossibly homozygous56733956
458757005875701CG24GENICpossibly homozygous56733957
458758685875869CA27GENICpossibly homozygous56733958
458760365876037T-25GENIChomozygous56733959
458760995876100GA19GENIChomozygous56733960
458761905876191TTCACA5GENICheterozygous56733961
458773715877372AT31GENICpossibly homozygous56733964
458791315879132AAT24GENICpossibly homozygous56733965
458808855880886CCT25GENIChomozygous56733966
458829525882953AG22GENIChomozygous56733967
458834375883438AG21GENIChomozygous56733968
458836695883670CG26GENIChomozygous56733969
458786505878693CCCAAAACATGTGCTTATATTTATTTACATTTACTGTAAAATG-------------------------------------------16GENICpossibly homozygous58325813