chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141446165414461655TC9GENIChomozygous125904452
141446169914461700AG6GENIChomozygous125904454
141446170814461709CG8GENIChomozygous125904456
141446324114463242CT14GENIChomozygous125904462
141446850614468507AC7GENIChomozygous125904464
141447233214472333TA6GENIChomozygous125904468
141450597814505979CA3GENICheterozygous125929926
141459771814597719TA3GENICheterozygous125929928
141460704214607043GT6GENIChomozygous125904504
141464228414642285TG17GENIChomozygous125904517
141464231014642311TG11GENIChomozygous125904519
141464240714642408TA17GENIChomozygous125904521
141464246314642464GA13GENIChomozygous125904523
141467759214677593AT6GENIChomozygous125904529
141467788514677886AC6GENIChomozygous125929931
141472067114720672GT6GENIChomozygous125904538
141472482714724828GC5GENIChomozygous125904540
141472690914726910CG8GENIChomozygous125904542