chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184060816540608166GT1GENIChomozygous623864669
184060913440609135AG9GENICheterozygous623864670
184060922040609221AG7GENIChomozygous623864671
184060963040609631AG2GENIChomozygous623864672
184061194540611946AG8GENIChomozygous623864673
184061233240612333GT6GENICheterozygous623864674
184061304940613050CA12GENICpossibly homozygous623864675
184061710140617102GA19GENICpossibly homozygous623864676
184061773440617735TC6GENIChomozygous623864677
184061774840617749GT12GENIChomozygous623864678
184061833040618331GA16GENICpossibly homozygous623864679
184061875240618753GA21GENICpossibly homozygous623864680
184061904140619042AG16GENICpossibly homozygous623864681
184061928940619290AG9GENICpossibly homozygous623864682
184062017040620171AG8GENICpossibly homozygous623864683
184062099840620999GA25GENIChomozygous623864684
184062283840622839AG12GENICpossibly homozygous623864685
184062301440623015GA12GENICpossibly homozygous623864686
184062450740624508TTTC5GENIChomozygous740361783
184062465840624659GC12GENIChomozygous623864687
184062598440625985GGA1GENIChomozygous740361784
184062819840628199GA24GENIChomozygous623864688
184062860140628602CT10GENICpossibly homozygous623864689
184063123440631235GA9GENIChomozygous623864690
184063172440631725GA11GENIChomozygous623864691
184063333540633336AC14GENIChomozygous623864692
184063387540633876GA13GENICheterozygous623864693