chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17237687872376879TG28GENICpossibly homozygous792302263
17237895772378958GA36GENIChomozygous792302264
17237943172379432TG8GENIChomozygous792302265
17237943272379433TC8GENIChomozygous792302266
17237943372379434TG8GENIChomozygous792302267
17237943572379436TA8GENIChomozygous792302268
17237986172379862AG32GENIChomozygous792302269