chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96031579060315791TC12GENIChomozygous138606461
96031609560316096AG7GENIChomozygous138606462
96031625260316253TG16GENIChomozygous138606463
96031736360317364TC18GENIChomozygous138606464
96031744460317447AAT15GENIChomozygous138466922
96031782160317822CT19GENIChomozygous138606465
96031838060318380TCT13GENIChomozygous138466923
96031901760319018G7GENIChomozygous138466924
96032030060320301TC32GENIChomozygous138606466
96032031760320318TG27GENIChomozygous138606467
96032180760321808TC17GENIChomozygous138606468
96032386560323866CT16GENIChomozygous138606469
96032455960324560CA20GENIChomozygous138606470
96032520860325209GC21GENIChomozygous138606471
96032615860326159G10GENIChomozygous138466925
96032618460326185TC10GENIChomozygous138606472
96032619260326193TC10GENIChomozygous138606473
96032628860326298CTAAGACTGC11GENIChomozygous138466926
96032671760326718TC8GENIChomozygous138606474
96032826560328265GAA9GENIChomozygous138466927
96032282960322830AT15GENICheterozygous154594264
96032282960322830A15GENIChomozygous403267001
96032906160329062CT12GENIChomozygous138606475
96032909260329093CT11GENIChomozygous138606476
96032921060329210T18GENIChomozygous138466928
96032998060329981TC10GENIChomozygous138606477
96033186560331866CT13GENIChomozygous138606478
96033342460333425CG12GENIChomozygous138606479
96033665960336660GA11GENIChomozygous138606480
96033701660337017CG11GENIChomozygous138606481
96033865660338656A11GENIChomozygous138466929
96034080860340808T20GENIChomozygous138466930
96034213160342131G13GENIChomozygous138466931
96034140260341403TC18GENIChomozygous138606482
96034204960342050TA8GENIChomozygous138606483
96034246060342461TC13GENIChomozygous138606484
96034252260342523CG11GENIChomozygous138606485
96034257760342578AT18GENIChomozygous138606486
96034257860342579TC18GENIChomozygous138606487