chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143184329143184330GT20GENICpossibly homozygous57506943
4143185628143185629C-18GENIChomozygous58082926
4143186668143186669TC15GENIChomozygous56961804
4143188708143188709TA19GENICpossibly homozygous56961813
4143190016143190017TC12GENICpossibly homozygous56961821
4143190292143190313CCTAAAAGTAACTTTATCTGG---------------------1GENIChomozygous58082927
4143191441143191442AG11GENICheterozygous56961826
4143191850143191851TA14GENICpossibly homozygous57506945
4143192114143192115GA19GENIChomozygous58082928
4143192203143192204AG15GENIChomozygous56961827
4143192669143192670GA27GENICpossibly homozygous57506947
4143192936143192937GA15GENICpossibly homozygous56961829
4143194567143194568CT16GENICpossibly homozygous57506949
4143195199143195200GT26GENIChomozygous56961831
4143196553143196554AAGT3GENIChomozygous58082929
4143196676143196677TC14GENIChomozygous58082930
4143196922143196923GC17GENICpossibly homozygous56961834
4143198336143198337GA9GENIChomozygous56961837
4143198859143198860TC22GENIChomozygous57944467
4143199361143199362CT20GENICheterozygous57944469
4143199990143199991TG23GENIChomozygous56961838
4143201099143201100AC27GENICpossibly homozygous56961840
4143201470143201471GT16GENICpossibly homozygous56961841
4143201924143201925TC20GENICpossibly homozygous56961842