chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37259031172590312GA32GENICpossibly homozygous111923510
37259070672590707CT40GENIChomozygous111608283
37259080672590807AG33GENIChomozygous111608284
37259099972591000AT19GENICpossibly homozygous119675505
37259118472591185TC12GENIChomozygous119675506
37259149472591495TC21GENIChomozygous111608285
37259179172591792AG36GENIChomozygous111608286
37259252772592528AG24GENIChomozygous111608288
37259256172592562TC30GENICpossibly homozygous111608289
37259259572592596GA27GENICpossibly homozygous111608290
37259262772592628TG25GENICpossibly homozygous111608291
37259369172593692CA23GENIChomozygous111608292
37259392772593928GA18GENIChomozygous111608293
37259448272594483TG20GENIChomozygous111608294
37259457672594577TC28GENIChomozygous111608295
37259489372594894CA26GENICpossibly homozygous111608297
37259516072595161CG22GENIChomozygous111608298
37259532772595328CT25GENIChomozygous111608300
37259536872595369AG25GENIChomozygous111608301
37259567872595679TG27GENIChomozygous111608302
37259601172596012CT25GENIChomozygous111608303
37259608572596086TC27GENIChomozygous111608304
37259622372596224TC26GENIChomozygous111608305
37259670872596709CT27GENICpossibly homozygous111608306
37259852472598525TA27GENIChomozygous111608307
37259886172598862TC28GENIChomozygous111608308
37260107972601080CT19GENIChomozygous119675507
37260110372601104TC18GENIChomozygous119675508
37260172372601724AG6GENIChomozygous112127666
37260227572602276CT19GENIChomozygous112127667
37260257872602579GA24GENIChomozygous112127668
37260299372602994TG27GENIChomozygous111608312
37260315572603156CT32GENIChomozygous112127669
37260409272604093AG15GENIChomozygous111608313
37260420872604209AT13GENIChomozygous111608314
37260459072604591CT13GENIChomozygous111608315