chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1112085506112085507CT32GENIChomozygous108182113
1112085637112085638TC30GENIChomozygous108182115
1112085671112085672GC23GENIChomozygous108182116
1112085868112085869AG26GENIChomozygous108182118
1112086575112086576CT36GENIChomozygous109123888
1112086900112086901CT23GENIChomozygous109123890
1112087117112087118CT9GENIChomozygous109123892
1112087266112087267TC13GENIChomozygous108182121
1112087625112087626TA20GENIChomozygous109123894
1112087630112087631GA20GENIChomozygous108182122
1112087977112087978GA25GENIChomozygous109123896
1112088215112088216GA28GENIChomozygous109123898
1112088581112088582AC25GENIChomozygous108182125
1112088847112088848AG17GENIChomozygous108182128
1112088848112088849AG17GENIChomozygous108182129
1112088868112088869GA23GENIChomozygous109123900
1112088876112088877AT22GENIChomozygous109123901