chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1127939352793936CT1GENIChomozygous51150371
1127940852794086AG4GENICheterozygous51063805
1127942502794251GC10GENIChomozygous51063808
1127948732794874AT6GENIChomozygous51150372
1127952082795209CG17GENICpossibly homozygous51150373
1127953692795370CA1GENIChomozygous51063828
1127956092795610GA6GENIChomozygous51063833
1127957292795730AC4GENICheterozygous51150374
1127957762795777GA6GENIChomozygous51063835
1127961452796146T-12GENIChomozygous51063845
1127967682796769TA4GENICheterozygous51150375
1127967752796780ATATT-----3GENICheterozygous51150376
1127969072796908GT2GENIChomozygous51063855
1127969092796910AT2GENIChomozygous51150377
1127970452797046CT15GENICpossibly homozygous51150378