chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37259031172590312GA16GENIChomozygous111923510
37259070672590707CT16GENIChomozygous111608283
37259080672590807AG17GENIChomozygous111608284
37259099972591000AT13GENIChomozygous119675505
37259118472591185TC8GENIChomozygous119675506
37259149472591495TC10GENIChomozygous111608285
37259179172591792AG8GENIChomozygous111608286
37259252772592528AG16GENIChomozygous111608288
37259256172592562TC14GENIChomozygous111608289
37259259572592596GA13GENIChomozygous111608290
37259262772592628TG10GENIChomozygous111608291
37259369172593692CA14GENIChomozygous111608292
37259392772593928GA10GENIChomozygous111608293
37259448272594483TG13GENIChomozygous111608294
37259457672594577TC11GENIChomozygous111608295
37259489372594894CA11GENIChomozygous111608297
37259516072595161CG12GENIChomozygous111608298
37259532772595328CT10GENIChomozygous111608300
37259536872595369AG12GENIChomozygous111608301
37259567872595679TG9GENIChomozygous111608302
37259601172596012CT15GENIChomozygous111608303
37259608572596086TC9GENIChomozygous111608304
37259622372596224TC12GENIChomozygous111608305
37259670872596709CT9GENIChomozygous111608306
37259852472598525TA15GENIChomozygous111608307
37259886172598862TC14GENIChomozygous111608308
37260107972601080CT10GENICpossibly homozygous119675507
37260110372601104TC10GENICpossibly homozygous119675508
37260172372601724AG7GENIChomozygous112127666
37260184072601841TC3GENIChomozygous111608310
37260227572602276CT7GENICpossibly homozygous112127667
37260257872602579GA19GENIChomozygous112127668
37260299372602994TG8GENIChomozygous111608312
37260315572603156CT8GENICpossibly homozygous112127669
37260409272604093AG6GENIChomozygous111608313
37260420872604209AT9GENIChomozygous111608314
37260459072604591CT3GENIChomozygous111608315