chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65077330350773304AT15GENIChomozygous966931509
65077445950774460AG32GENIChomozygous966931510
65077452650774527TC38GENIChomozygous966931511
65077597650775977GA46GENIChomozygous966931512
65077644450776445CT18GENIChomozygous966931513
65077671050776711CT23GENIChomozygous966931514
65077698850776989GA15GENICpossibly homozygous966931515
65077786450777865GA12GENIChomozygous966931516
65077907450779075CT28GENIChomozygous966931517
65077909450779095AG32GENIChomozygous966931518
65078189350781894AG37GENICpossibly homozygous966931519
65078208950782090TC31GENIChomozygous966931520
65078330950783310AG26GENIChomozygous966931521
65078338050783381AT20GENIChomozygous966931522
65078358850783589AG25GENICpossibly homozygous966931523