chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135270786652707867CT27GENIChomozygous50230440
135270849652708498AA--11GENIChomozygous49948652
135270854752708548TC18GENIChomozygous50040672
135270886552708866CT20GENIChomozygous50040674
135270964252709643AG26GENIChomozygous49948659
135270992152709922AG24GENIChomozygous49948660
135271018052710181GA24GENIChomozygous50361177
135271068652710687GA15GENIChomozygous49948661
135271071952710723CACA----9GENIChomozygous50563178
135271087152710872GA30GENIChomozygous49948662
135271102552711026GC25GENIChomozygous49948663
135271123052711231GA25GENIChomozygous49948664
135271125052711251CT31GENIChomozygous49948665
135271134152711342CT21GENIChomozygous49948666
135271135552711356TC24GENIChomozygous49948667
135271138052711381TC29GENIChomozygous49948669
135271163352711634CA29GENIChomozygous49948670
135271179152711792GA21GENIChomozygous49948671
135271180252711803AG18GENIChomozygous49948672
135271182152711822AG20GENIChomozygous49948673
135271185752711858GA25GENICpossibly homozygous49948674
135271214952712150TC27GENIChomozygous49948676
135271226952712270CT35GENIChomozygous49948677
135271236252712363TC30GENIChomozygous49948678
135271242952712430GA26GENIChomozygous49948680