chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2094183379418338TTGAGTGTTGA25GENIChomozygous45679705
2094183679418368GA23GENIChomozygous45789897
2094183829418383GA25GENIChomozygous45789898
2094183839418384GA25GENIChomozygous45679706
2094184339418434TG20GENIChomozygous45679708
2094186469418647TA22GENIChomozygous45679710
2094190899419090AAC55GENIChomozygous45789899
2094192259419226TA38GENIChomozygous45679712
2094192319419249GATGTAGGCTTACACTCA------------------43GENIChomozygous45679714
2094194179419418GA32GENIChomozygous45679717
2094195099419510AG27GENIChomozygous45679719
2094202849420285GA25GENIChomozygous45679720
2094202939420294CT27GENIChomozygous45679722
2094203139420314CT19GENIChomozygous45679723
2094203239420324TC19GENIChomozygous45679725
2094203509420357TTTTTTT-------14GENIChomozygous45679727
2094203689420369CCT11GENIChomozygous45679728
2094204229420423AG17GENIChomozygous45679730
2094207609420761TA23GENIChomozygous45679733
2094208899420890GGTCAA26GENICpossibly homozygous45679735
2094209499420950GA25GENIChomozygous45679736
2094209909420991AT23GENICpossibly homozygous45679738
2094210149421015AG28GENICpossibly homozygous45679739
2094211609421161CCCT37GENICpossibly homozygous45679741
2094212359421236CT35GENICpossibly homozygous45679743
2094213929421393AG26GENICpossibly homozygous45679744
2094218679421868GA27GENIChomozygous45679746
2094219169421917TA22GENIChomozygous45679747
2094219479421948TG25GENIChomozygous45679749
2094221539422154TC21GENIChomozygous45789900
2094221609422161TC20GENIChomozygous45423424
2094222179422218CT19GENIChomozygous45679753
2094222369422237GA13GENIChomozygous45679754
2094225109422511CT5GENIChomozygous45789901
2094225119422512GGC5GENIChomozygous45679759
2094225609422561AG4GENIChomozygous45789902
2094225839422584CG5GENIChomozygous45423426
2094223399422340G-7GENIChomozygous45855945
2094203609420361TC12GENIChomozygous45819182