chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121125243011252430AGGC68GENIChomozygous128959439
121125412811254129AG60GENIChomozygous115415385
121125418211254183CT66GENIChomozygous115415387
121125418411254185TC65GENIChomozygous115415389
121125459411254595TC63GENIChomozygous115415391
121125526011255260AAGAGGGTCCTCCCCA58GENIChomozygous128959442
121125558311255584AT73GENIChomozygous115254928
121125560111255602AG77GENIChomozygous115254930
121125585511255856CT52GENIChomozygous115415393
121125594111255942CT52GENIChomozygous115415395
121125599211255993AG48GENIChomozygous115254934
121125608111256086GCCCC54GENIChomozygous128959444
121125632211256323GA55GENIChomozygous115415397
121125684611256847TG61GENIChomozygous115254936
121125686711256868TC62GENIChomozygous115254938
121125711611257117AC59GENIChomozygous115254942
121125754411257545AG60GENIChomozygous115254944
121125755011257551AG57GENIChomozygous115254946
121125778411257785GA28GENIChomozygous115415399
121125790011257900AG50GENIChomozygous128959445
121125886211258863AC52GENIChomozygous115361399
121125989011259891GA58GENIChomozygous115254952
121126014611260147AG36GENIChomozygous115254954
121126044311260444AG36GENIChomozygous115254956
121126060611260607GA52GENIChomozygous115415403
121126105011261051CT48GENIChomozygous115254958
121126109611261097TC47GENIChomozygous115254960
121126124811261249GC69GENIChomozygous115415405
121126127211261273TA53GENIChomozygous115415407
121126127311261274TA53GENIChomozygous115415409
121126133311261334GA59GENIChomozygous115415412
121126163111261632AT51GENIChomozygous115254962
121126312711263128AT30GENIChomozygous115521329
121126379511263796TG54GENIChomozygous115254970
121126433511264335T31GENIChomozygous128959449
121126433611264337GA35GENIChomozygous115254974
121126505211265053CA46GENIChomozygous115254980
121126534711265348AG52GENIChomozygous115254984
121125962111259622A43GENIChomozygous132165316
121126416611264174GCTCGTGT31GENIChomozygous132165317
121126534511265345GA52GENIChomozygous132165318