chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135270820652708207CT33GENIChomozygous50931820
135270850252708507AAAAT-----15GENIChomozygous50931823
135270854752708548TC15GENIChomozygous50040672
135270964252709643AG23GENICpossibly homozygous49948659
135270992152709922AG24GENIChomozygous49948660
135271068652710687GA16GENIChomozygous49948661
135271087152710872GA25GENIChomozygous49948662
135271102552711026GC18GENIChomozygous49948663
135271123052711231GA21GENICpossibly homozygous49948664
135271125052711251CT22GENICpossibly homozygous49948665
135271134152711342CT16GENIChomozygous49948666
135271135552711356TC16GENIChomozygous49948667
135271138052711381TC20GENICpossibly homozygous49948669
135271163352711634CA21GENICpossibly homozygous49948670
135271179152711792GA24GENICpossibly homozygous49948671
135271180252711803AG28GENIChomozygous49948672
135271182152711822AG27GENIChomozygous49948673
135271185752711858GA35GENIChomozygous49948674
135271192652711927CT22GENIChomozygous50931826
135271214952712150TC22GENICpossibly homozygous49948676
135271226952712270CT25GENICpossibly homozygous49948677
135271236252712363TC14GENICpossibly homozygous49948678
135271242952712430GA40GENICpossibly homozygous49948680
135271018052710181GA21GENICpossibly homozygous50361177