chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
59226907592269076GT5GENIChomozygous56039329
59226961292269613CCG4GENIChomozygous56039330
59226974992269750AG7GENIChomozygous56170163
59226982092269821CT13GENIChomozygous56039331
59227056392270564GT6GENIChomozygous56039333
59227058392270588TTCTG-----5GENIChomozygous56039334
59227072392270724TC16GENIChomozygous56039335
59227105092271051AG8GENIChomozygous56039336
59227108992271090GA13GENIChomozygous56039337
59227132292271323TTA10GENIChomozygous56039338
59227250592272506CT31GENIChomozygous56039339
59227279092272791GT26GENICpossibly homozygous56039340
59227283892272839GT24GENIChomozygous56039341
59227291392272914AG14GENIChomozygous56039342
59227383292273833TC6GENIChomozygous56039343
59227418892274189CT13GENIChomozygous55559943
59227459892274599GA27GENICpossibly homozygous56039344
59227464592274646AC23GENIChomozygous56039345
59227492292274923AG21GENIChomozygous56039346
59227506992275070GA12GENIChomozygous56039347
59227522792275228CT11GENIChomozygous56170165
59227571492275715TG8GENIChomozygous56039348
59227602792276028GA14GENIChomozygous56039349
59227660492276605CG11GENIChomozygous56039350